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Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.



Solubility
&
Precipitation                         Compare and Contrast


                                                 Solubility
                                                        vs
                                              Precipitation
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.

                              • When a solute dissolves in a solvent,
The                             the individual particles of the solute
Solution                        separate from the other particles of
Process                         the solute and move between the
                                spaces of the solvent particles. The
                                solvent particles collide with the
A Review from                   solute particles and forces of
Chemistry 30S                   attraction between solute and solvent
                                particles "hold" the solute particles in
                                the spaces.
                              • For a solute to be dissolved in a
                                solvent, the attractive forces between
                                the solute and solvent molecules
                                must be greater than the forces of
                                attraction between the solute
                                molecules.
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.

                              1. The solvent particles must move apart to
The                              make room for solute particles. This
                                 process requires energy to overcome
Solution                         forces of attraction between solvent
Process                          particles. The first step in the dissolving
                                 process is endothermic.
A 3 Step                      2. The solute particles must separate form
                                 the other solute particles. This process
Process                          also requires energy to overcome the
                                 forces of attraction between the solute
                                 particles. The second step in the dissolving
                                 process is endothermic.
                              3. When the solute particles move between
                                 the solvent particles the forces of attraction
                                 between solute and solvent take hold and
                                 the particles "snap" back and move closer.
                                 This process releases energy. The final
                                 step in the dissolving process is
                                 exothermic.
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.

                              • The total heat change in the
Energy                          dissolving process is the sum of the
Changes                         three heat changes. If the sum of
During                          the heat absorbed in the first two
Dissolving                      steps of the dissolving process is
                                greater than the heat released in the
                                last step, the dissolving of that
                                substance will be endothermic. If
                                the dissolving process for a
                                substance is endothermic, the
                                container will feel cooler as the
                                substance dissolves.
                              • In some cases, the exothermic
                                process is larger than the sum of
                                the two endothermic processes. In
                                these cases, as the solid dissolves
                                large amounts of heat are evolved.
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.

                              • When we talk about the mixing of two
Solubility                      or more substances together in solution
                                we must consider solubility. Simply
                                defined, it is a measure of how much
                                solute will dissolve into the solvent. Not
                                all substances will dissolve in all
                                solvents.
                              • Example 1: NaCl(s) dissolved in water
                                Molecular level:




                                 NaCl (solid) + H2O (liquid)       NaCl(aq)
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.


                              Student TASK
Solubility
                              • Create a series of drawings that outline
                                what happens in the solution process
                                involving NaCl dissolving in water.
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.


                              • Example 1: NaCl(s) dissolved in water
Solubility
                                 Symbolic level:

                                 NaCl(s) → NaCl(aq)
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.


                              • A precipitation reaction is a common
Precipitation                   type of chemical reaction in solution
                                chemistry. Basically, two or more
                                solutions are combined resulting in a
                                reaction that produces an insoluble
                                product, a precipitate. Typically, these
                                types of reactions involve ionic
                                compounds in aqueous solution. The
                                precipitation reaction is said to occur
                                because of the strong attractive forces
                                certain ions have for each other. These
                                ions combine and fall out of solution in
                                the formation of a solid.
                              • The ability to predict precipitate
                                formation is based upon solubility.
                                When the product of a reaction is
                                insoluble, it precipitates.
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.

                              •   Example 1: NaCl(s) and AgNO3 combined together
Precipitation                     Molecular level:




                              •
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.

                              •   Example 1: NaCl(s) and AgNO3 combined together
Precipitation                     Molecular level:




                              •
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.


                              Student TASK
Precipitation
                              • Create a series of 3 diagrams that
                                outline what happens when NaCl and
                                AgNO3 are combined in a precipitation
                                reaction.

                                 Diagram 1 – draw Na+ and Cl- ions
                                 circulating amidst the water molecules
                                 Diagram 2 – AgNO3 is drawn with the
                                 Ag+ and NO3- ions floating around the
                                 water molecules
                                 Diagram 3 – Shows the mixing of the
                                 two solutions. The Ag+ and Cl-
                                 combine to form a precipitate.
Outcome 1-01
 Explain observed examples of solubility and precipitation at the molecular and symbolic
 levels.



 Precipitation

• Symbolic level:

  Molecular equation:
        NaCl (aq) + AgNO3 (aq) → AgCl (s) + NaNO3 (aq)

  Ionic equation:
        Na+ (aq) + Cl- (aq) + Ag+ (aq) + NO3- (aq) → AgCl (s) + Na+ (aq) + NO3- (aq)

  Net ionic equation:
        Ag+ (aq) + Cl- (aq) → AgCl (s)
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.


Precipitation • When certain solutions of electrolytes
                                are mixed, the cation of one solute may
                                combine with the anion of the other
How to write                    solute to form an insoluble compound.
chemical                        This leads to the formation of a
equations for                   precipitate.
precipitation                 • A precipitate is an insoluble solid that
reactions                       settles from a solution. For instance,
                                when a solution of Pb(NO3)2 is mixed
                                with a solution of HCl, a precipitate of
                                insoluble PbCl2(s) forms. This occurs
                                because combining the solutions
                                results in a new solution containing
                                more PbCl2(aq) than is soluble. A
                                condition referred to as
                                supersaturation. In this case, solid
                                PbCl2 must settle out of the solution.
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.


                              • In the molecular equation the
Precipitation                   formulas of the compounds are written
                                as their usual chemical formulas.

                                 Pb(NO3)2 (aq) + 2HCl (aq)             PbCl2 (s) +
                                 2HNO3 (aq)

                              • The precipitation reaction is more
                                accurately represented by the ionic
                                equation. The ionic equation shows
                                the compounds as being dissociated in
                                solution.

                                 Pb2+ (aq) + 2NO3- (aq) + 2H+ (aq) + 2Cl– (aq)
                                     PbCl2 (s) + 2H+ (aq) + 2NO3- (aq)
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.



Precipitation                    Pb2+ (aq) + 2NO3- (aq) + 2H+ (aq) + 2Cl– (aq)
                                       PbCl2 (s) + 2H+ (aq) + 2NO3- (aq)
                              • If you examine the ionic equation, you
                                will notice that the H+ ions and NO3-ions
                                are not involved in the formation of the
                                precipitate. We refer to the ions which
                                are not involved in the reaction as
                                spectator ions. Identical species on
                                both sides of the equation can be
                                omitted from the equation. The net
                                ionic equation shows only the species
                                that actually undergo a chemical
                                change.
                                Pb2+ (aq) + 2Cl– (aq)      PbCl2 (s)
                              • In order to predict whether a precipitate
                                will form when two solutions are mixed,
                                you need to know the solubility rules for
                                ionic compounds.
Outcome 1-01
Explain observed examples of solubility and precipitation at the molecular and symbolic
levels.



Precipitation
Outcome 1-02
Perform a lab to develop a set of solubility rules.
Outcome 1-03
Use a table of solubility rules to predict the formation of a precipitate.


Solubility
Rules
Outcome 1-02
Perform a lab to develop a set of solubility rules.
Outcome 1-03
Use a table of solubility rules to predict the formation of a precipitate.

Process
Notes for
Writing Net
Ionic
Equations
Rules
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a
strong acid.



Acid/Base                              Definitions of acids and bases
Review                                 • Arrhenius
                                         acid: generates [H+] in solution
                                         base: generates [OH-] in solution
                                       • normal Arrhenius equation:
                                         acid + base     salt + water

                                       • example: HCl + NaOH                              NaCl + H2O
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a
strong acid.



Acid/Base                              • A strong acid is defined as an
Review                                   acid that completely dissociates
                                         into ions. This means that if there
                                         are 100 molecules of HCl
                                         dissolved in water, 100 ions of H+
                                         and 100 ions of Cl- are produced.
                                       • It should be stressed that there
                                         are only 6 strong acids. These
                                         are:
                                           –   hydrochloric acid (HCl),
                                           –   hydrobromic acid (HBr),
                                           –   hydroiodic acid (HI),
                                           –   sulfuric acid (H2SO4),
                                           –   nitric acid (HNO3),
                                           –   perchloric acid (HClO4).
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
strong acid.



Acid/Base                              • A strong base is defined as a
Review                                   base that completely dissociates
                                         into ions. This means that if
                                         there are 100 formula units of
                                         NaOH dissolved in water, 100
                                         ions of Na+ and 100 ions of OH-
                                         are produced.
                                       • Strong bases include any ionic
                                         compound that contains the
                                         hydroxide (OH-) ion.
                                       • When combined with the
                                         hydroxide ion, elements found in
                                         groups 1 and 2 form strong
                                         bases.
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
strong acid.


Naming Acids                           • To name a binary acid follow the
                                         steps given:
                                         1. the prefix "hydro" is used
                                         2. the root of the anion is used
                                         3. the suffix "ic" is used
                                         4. the word "acid" is used as the
                                         second word in the name
                                       • Example of naming a binary acid:
                                         HCl
                                         Step 1: hydro-
                                         Step 2: -chloride
                                         Step 3: -chloric
                                         Step 4: hydrochloric acid
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
strong acid.


Naming Acids                           • Naming polyatomic acids follow a different
                                         set of rules. Many of the oxygen-rich
                                         polyatomic negative ions form acids that are
                                         named by replacing the suffix -ate with -ic
                                         and the suffix -ite with -ous.
                                       • To name oxyacids (acids containing the
                                         element oxygen) you recognize them by the
                                         general formula HaXbOc where X represents
                                         an element other than hydrogen or oxygen. If
                                         enough H+ ions are added to a (root)ate
                                         polyatomic ion to completely neutralize its
                                         charge, the (root)ic acid is formed
                                       • Examples of polyatomic acids:
                                         – If one H+ ion is added to nitrate, NO3-
                                         – HNO3 is formed. This is named nitric
                                            acid.
                                         – If two H+ ions are added to sulfate,
                                            SO42-
                                         – H2SO4 is formed. This is named
                                            sulfuric acid.
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
strong acid.



Neutralization                         • Most common acid-base
Reactions                                reactions take place in water
                                         solutions (commonly referred to
                                         as aqueous solutions).
                                       • In the reaction of an acid with a
                                         base in aqueous solution, the
                                         hydrogen ions of the acid react
                                         with the hydroxide ions of the
                                         base to give water. The second
                                         product is a salt, which is
                                         composed of the positive metal
                                         ion from the base and the
                                         negative ion from the acid.
                                       • In general, the reaction for a
                                         neutralization reaction is given by
                                            acid + base → salt + water
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
strong acid.



Neutralization                         • For example,
Reactions                              • HCl(aq) + KOH(aq) → H2O(l) + KCl(aq)
                                       • Since HCl(aq) and KOH(aq) are fully
                                         ionized in solution, the preceding
                                         equation can be written as
                                       • H+ (aq) + Cl− (aq) K+(aq) + OH−(aq) → H2O (l)
                                         K+(aq) + Cl−(aq)
                                       • Ions common to both sides (spectator
                                         ions) can be canceled to yield
                                       • H+(aq) + OH−(aq) → H2O(l)
                                       • This is referred to as the net ionic
                                         equation for the neutralization
                                         reaction. If H3O+ is substituted for H+
                                         (aq) the neutralization equation
                                         becomes
                                       • H3O+(aq) + OH−(aq) → 2 H2O (l)
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
strong acid.


Process
Notes for
Writing Net
Ionic
Equations
Rules
Outcome 1-04
Write balanced neutralization reactions involving strong acids and bases.
Outcome 1-05
Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
strong acid.


Process
Notes for
Writing Net
Ionic
Equations
Rules
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titrations                             • A titration is a carefully
                                            controlled neutralization
                                            reaction.
                                          • To perform a titration, a
                                            standard solution is required. A
                                            standard solution is a solution
                                            of a strong acid or base of
                                            known concentration. To
                                            determine the concentration of
                                            an acid, a basic standard
                                            solution is required, and vice
                                            versa for an unknown base. The
                                            standard solution is usually
                                            added to a sample of unknown
                                            concentration, until
                                            neutralization has occurred.
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titrations                           • A buret is used to control the
                                          additions of acids and bases in a
                                          titration. The buret determines the
                                          volumes of acids and bases added
                                          in a titration.
                                        • If you recall, when an acid or base
                                          is just neutralized, the moles of
                                          hydronium ions from the acid and
                                          moles of hydroxide ions from the
                                          base are equal. The point at which
                                          the amount of standard acid or
                                          base solution added just neutralizes
                                          the unknown sample is called the
                                          equivalence point.
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titrations                              • The equivalence point can be
                                             determined by adding a pH indicator to
                                             the unknown sample or by using a pH
                                             meter to measure the pH change as
                                             standard solution is added to the
                                             sample. If an indicator is used, the point
                                             in the titration at which the desired
                                             colour forms is called the endpoint of
                                             the titration. The indicator is chosen so
                                             that the endpoint and the equivalence
                                             point are very close.
                                           • The endpoint and the equivalence point
                                             are NOT the same thing. The
                                             equivalence point is a single point
                                             defined by the reaction stoichiometry.
                                             The endpoint is determined by the
                                             choice of indicators.
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titrations                            Titration Procedure
                                         • When performing an acid-base titration on an
                                           unknown solution, both the standard and
                                           unknown solutions are placed into separate
                                           burets. For this example, we will determine
                                           the concentration of a hydrochloric acid
                                           solution using a 0.100 mol/L solution of
                                           NaOH.
                                         • Each buret is filled and the initial volume
                                           readings are taken from the bottom of the
                                           meniscus (the smile-shaped surface of the
                                           solution in the container).
                                         • A sample or aliquot of the acid solution is
                                           released into an Erlenmeyer flask. The acid
                                           volume in the buret is read and called the
                                           "final acid volume". The volume of the aliquot
                                           is equal to:
                                            final volume reading - initial volume reading
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titrations                           Titration Procedure - continued
                                        • We will use phenolphthalein as our
                                          indicator. The endpoint will be reached
                                          when the sample turns a light pink. Even
                                          though phenolphthalein turns pink at a pH
                                          of about 8.2, this is not a significant
                                          problem, as we will see later.
                                        • We slowly add the standard base solution
                                          to the flask, with stirring or swirling, until
                                          the solution in the flask turns (and stays) a
                                          light pink. We take the reading on the
                                          base buret and call this the "final base
                                          volume".
                                        • This procedure is repeated until there are
                                          several pieces of consistent data.
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titration
   Procedure
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titration
   Video
   Demo
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.


   Determining                         Example 1
   Concentratio
   n                                   • A titration was performed using a standard
                                         solution of 0.100 mol/L NaOH into and
                                         unknown HCl solution. The following data was
                                         collected:

                                                                         Base                    Acid
                                         Final Volume Reading            14.45 mL                12.57 mL
                                         Initial Volume Reading          0.62 mL                 1.13 mL

                                       Determine the concentration of the acid.
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



  Determini                               Example 2
  ng the
  Mass of                                 • A student receives a solid
  an                                        sample of sulfamic acid (molar
  unknown                                   mass is 97.09 g/mol), a
  Sample                                    monoprotic acid, and dissolves
                                            the sample in enough water to
                                            make 100.0 mL of solution. The
                                            students takes a 12.00 mL
                                            aliquot and titrates with 0.0985
                                            mol/L sodium hydroxide. If
                                            13.38 mL of the base is needed
                                            to reach the endpoint, what is
                                            the mass of the sample of acid?
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titration                             • If pH readings are taken during a
   Curves                                  titration and those pH values are
                                           plotted, a titration curve is
                                           generated. The general shape of the
                                           curves generated may be grouped
                                           into families, according to the solution
                                           titrated and the titrating solutions. We
                                           will discuss four classes of titrations:
                                            –1. Strong acid titrated with strong
                                              base.
                                            –2. Strong base titrated with
                                              strong acid.
                                            –3. Weak acid titrated with strong
                                              base.
                                            –4. Weak base titrated with strong
                                              acid.
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a
 strong acid.



   Titration                            1. Strong Acid Titrated with a Strong Base
   Curves
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titration                             2. Strong Base Titrated with a Strong Acid
   Curves
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titration                             3. Titration of a Weak Acid with a Strong Base
   Curves
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titration                             4. Titration of a Weak Base with a Strong Acid
   Curves
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a
 strong acid.



   Titration
   Curves
Chemistry 40S
 Outcome 1-04                                                         Unit 3 – Acid/Base
Equilibria neutralization reactions involving strong acids and bases.
 Write balanced
 Outcome 1-05
 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a
 strong acid.



   Titration
   Curves
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation                            What is oxidation and reduction?
  Reduction
                                       • The term “oxidation” was first applied
                                         to the combining of oxygen with other
                                         elements (ex. rusting iron or burning
                                         carbon or methane). Burning is
                                         another name for rapid oxidation.
                                       • The term “reduction” originally meant
                                         the removal of oxygen from a
                                         compound. The term reduction comes
                                         from the fact that the free metal has a
                                         lower mass than its oxide compound.
                                         There is a decrease or reduction in
                                         the mass of the material as the
                                         oxygen is removed.
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation                            What is oxidation and reduction?
  Reduction
                                       • Chemists recognized that other
                                         nonmetallic elements unite with
                                         substances in a manner similar to that
                                         of oxygen (ex. hydrogen, antimony,
                                         and sodium will burn in chlorine; iron
                                         will burn in fluorine).
                                       • Therefore, the term oxidation was
                                         redefined as the process by which
                                         electrons are removed from an
                                         atom or ion.
                                       • Reduction was then defined as the
                                         process by which any atom or ion
                                         gains electrons.
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation
  Reduction
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation                            What is oxidation and reduction?
  Reduction
                                       • Oxidation occurs when an atom loses
                                         one or more electrons and reduction
                                         is when an atom gains one or more
                                         electrons. There are two mnemonics
                                         to help us remember these terms:

                                       • "OIL RIG": Oxidation Is Losing
                                         electrons, Reduction Is Gaining
                                         electrons
                                                          Or

                                       • "LEO says GER": Losing Electrons is
                                         Oxidation, Gaining Electrons is
                                         Reduction
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation-                           What are REDOX Reactions?
  Reduction                            • Oxidation-Reduction reactions, or
  Reactions                              Redox reactions, are defined as
                                         chemical changes that occur when
                                         electrons are transferred from one
                                         reactant to another.
                                       • For example,
                                                 2 Mg(s) + O2(g) → 2 MgO(s)
                                       • If this reaction is written in ionic form it
                                         becomes:
                                                  2 Mg0 + O20 → Mg2+ O2-
                                       • Magnesium and oxygen gases are
                                         both elements and have no charge
                                       • Non-scientists usually refer to this
                                         reaction as burning or combustion but
                                         as scientists, we refer to this reaction
                                         as oxidation.
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation-                           What are REDOX Reactions?
  Reduction                            • For example,
  Reactions                                     2 Mg(s) + O2(g) → 2 MgO(s)
                                       • We say that the magnesium has been
                                         oxidized to MgO by the reaction with
                                         oxygen gas
                                       • Considering the charges, the metal
                                         has gone from a 0 charge to 2+ and
                                         the non-metal from 0 charge to 2-
                                       • In this reaction magnesium begins as
                                         a neutral atom and loses two
                                         electrons to become a Mg2+ ion in
                                         MgO. Magnesium is oxidized. Oxygen
                                         begins as a neutral atom and gains
                                         the two electrons from magnesium to
                                         become an O2-¯ion in MgO. Oxygen is
                                         reduced.
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation-                           What are REDOX Reactions?
  Reduction                            • For example,
  Reactions
                                                   2 Mg(s) + O2(g) → 2 MgO(s)

                                       • If we look at the change in ion charge
                                         as a function of electrons, the
                                         following relationships can be written:
                                       • 2 Mg → 2Mg 2+ + 4 e- in this equation,
                                         charge is conserved, 0 charge on both
                                         sides
                                       • O2 + 4 e- → 2O 2- in this equation,
                                         charge is conserved, 4- charge on
                                         both sides
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation-                           What are REDOX Reactions?
  Reduction
  Reactions                            • Similarly, the reaction of magnesium
                                         combining with chlorine to produce
                                         magnesium chloride is also a redox
                                         reaction.

                                                     Mg(s) + Cl2(g) → MgCl2(s)

                                       • Magnesium loses two electrons to
                                         become a Mg2+ ion and is oxidized.
                                         Each chlorine atom gains one electron
                                         from magnesium to become Cl- ions.
                                         Each chlorine atom is reduced.
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation-                           What are REDOX Reactions?
  Reduction
  Reactions
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidation-                           What are REDOX Reactions?
  Reduction
  Reactions
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Reducing                             What are Reducing Agents?
  Agents
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Oxidizing                            What are Oxidizing Agents?
  Agents
Chemistry 40S                                                            Unit 3 – Acid/Base
Equilibria1-08
 Outcome
 Define oxidation and reduction.
 Include: gain and loss of electrons, oxidizing agent, reducing agent.



  Reducing                             What are Reducing & Oxidizing
  &                                     Agents?
  Oxidizing
  Agents                               • Any substance which causes the
                                         reduction of another substance is
                                         called the reducing agent.

                                       • Any substance which causes the
                                         oxidation of another substance is
                                         called an oxidizing agent.

                                                   2 Mg(s) + O2(g) → 2 MgO(s)
Chemistry 40S                                                   Unit 3 – Acid/Base
Equilibria1-09
 Outcome
 Determine the oxidation numbers for atoms in compounds and ions.




  Oxidation                         Assigning Oxidation Numbers
  Numbers
                                    • The oxidation number represents the
                                      charge the atom would have if every
                                      bond were ionic. Not every bond is
                                      ionic, but chemists assume they are
                                      for this system. The oxidation number
                                      is not always the actual charge, but it
                                      is very helpful to follow electrons in
                                      redox reactions.
Chemistry 40S                                                   Unit 3 – Acid/Base
Equilibria1-09
 Outcome
 Determine the oxidation numbers for atoms in compounds and ions.




  Oxidation                         Assigning Oxidation Numbers
  Numbers                              – Oxidation numbers are always
                                         assigned PER ATOM.
                                       – The oxidation numbers of all
                                         uncombined elements is zero. (ex. O2,
                                         K(s), H2,
                                       – The oxidation number of monatomic
                                         ions equals the charge of that ion.
                                       – In compounds, the oxidation number
                                         for alkali metals (ex. Li, Na, K, etc.) is
                                         always +1.
                                       – In compounds, the oxidation number
                                         for the alkaline earth metals (ex. Be,
                                         Mg, Ca, etc.) is always +2.
                                       – In compounds, the oxidation number
                                         of aluminum is always +3.
Chemistry 40S                                                   Unit 3 – Acid/Base
Equilibria1-09
 Outcome
 Determine the oxidation numbers for atoms in compounds and ions.




  Oxidation                         Assigning Oxidation Numbers
  Numbers                              – In compounds, the oxidation number of
                                         fluorine is -1.
                                       – In compounds, the oxidation number of
                                         hydrogen is +1. An exception is in metal
                                         hydrides, such as NaH or MgH2, when
                                         hydrogen is -1.
                                       – In compounds, the oxidation number of oxygen
                                         is -2. An exception is in peroxides, such as
                                         H2O2 or Na2O2, when its oxidation number is
                                         -1.
                                       – For any neutral compound, the sum of the
                                         oxidation numbers for each atom must be
                                         zero.
                                       – For a poly atomic ion, the sum of the oxidation
                                         numbers for each atom must be the charge of
                                         that ion.

                                         Note the difference between ion charge and
                                                        oxidation numbers:
                                           for example, the magnesium ion, Mg 2+
                                                        ion charge = 2+
                                                   oxidation number = +2
Chemistry 40S                                                     Unit 3 – Acid/Base
Equilibria1-10
 Outcome
 Identify and describe reactions as redox or non-redox.
 Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance



  Redox                              Recognizing Redox Reactions
  Reactions
                                        • In order to recognize a redox
                                          reaction, we must follow the
                                          electrons. We can follow the
                                          electrons by determining if
                                          the oxidation numbers
                                          change. If no oxidation
                                          numbers change, the reaction
                                          is NOT a redox reaction.
Chemistry 40S                                                     Unit 3 – Acid/Base
Equilibria1-10
 Outcome
 Identify and describe reactions as redox or non-redox.
 Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance



  Redox                              Recognizing Redox Reactions
  Reactions
                                        Example
                                        – Is the reaction below a redox reaction?
                                                       SO2 + H2O → H2SO3

                                        Solution
                                        – If we assign oxidation numbers to each atom,
                                           we find



                                        – the oxidation number of S remains at +4 in the
                                          reactants and in the products,
                                        – O remains unchanged in the products at -2
                                          and H remains unchanged at +1.
                                        – The oxidation numbers do not change, so
                                          electrons were not transferred. Therefore, this
                                          is not a redox reaction.
Chemistry 40S                                                     Unit 3 – Acid/Base
Equilibria1-10
 Outcome
 Identify and describe reactions as redox or non-redox.
 Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance



  Redox                              Recognizing Redox Reactions
  Reactions
                                        Example
                                        – Is the reaction below a redox reaction?
                                         Cu(s) + 2AgNO3(aq) → Cu(NO3)2(aq) + 2 Ag(s)

                                        Solution
                                        – Assign oxidation numbers to each atom,




                                        – Cu is zero in the reactants and +2 in the
                                          products.
                                        – Ag is +1 in the reactants and zero in the
                                          products.
                                        – N = +5 in both products and reactants.
                                        – O = -2 in both products and reactants.
Chemistry 40S                                                     Unit 3 – Acid/Base
Equilibria1-10
 Outcome
 Identify and describe reactions as redox or non-redox.
 Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance



  Redox                              Recognizing Redox Reactions
  Reactions
                                        Example
                                        – Is the reaction below a redox reaction?
                                         Cu(s) + 2AgNO3(aq) → Cu(NO3)2(aq) + 2 Ag(s)

                                        Solution




                                        – This is redox reaction, since the oxidation
                                          numbers of Cu and Ag change.
                                        – Cu is oxidized because its oxidation number
                                          becomes more positive, indicating it has lost
                                          electrons. .
                                        – The oxidation number of Ag becomes more
                                          negative, indicating a gain of electrons. Ag is
                                          reduced.
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Balancing Redox Reactions
  Redox
  Reactions                          • Redox reactions transfer electrons
                                       from one substance to another.
                                       Balancing a redox reaction balances
                                       the number of electrons lost and
                                       gained, then ensures the reaction
                                       obeys the Law of Conservation of
                                       Mass.

                                     • There are two methods we will use to
                                       balance redox reactions:

                                        – Oxidation Number Method
                                        – Half-Reactions Method
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Oxidation Number Method
  Redox
  Reactions                          • We will learn this method by balancing
                                                the following reaction:
                                        K2Cr2O7 + H2O + S       SO2 + KOH + Cr2O3

                                     • Step 1: Assign oxidation numbers.



                                     • Eventually, you will be able to
                                       recognize those just substances that
                                       are oxidized and reduced. You can
                                       just label those substances.
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Oxidation Number Method
  Redox                                 K2Cr2O7 + H2O + S       SO2 + KOH + Cr2O3
  Reactions
                                     • Step 2: Identify substances oxidized
                                       and reduced, then balance electrons
                                       lost and gained.




                                     • S is oxidized and Cr is reduced.
                                     • Notice that there are two Cr atoms
                                       and each gains three electrons, for a
                                       total of six.
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Oxidation Number Method
  Redox                                 K2Cr2O7 + H2O + S       SO2 + KOH + Cr2O3
  Reactions
                                     • Step 2 (continued): We then
                                       determine the lowest common multiple
                                       of 6 and 4, which is 12. We multiply
                                       the S atoms by 3 and the Cr atoms by
                                       2, so the total number of electrons lost
                                       and gained is 12.
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Oxidation Number Method
  Redox                                  K2Cr2O7 + H2O + S       SO2 + KOH + Cr2O3
  Reactions
                                     • Step 3: Balance all other atoms by
                                       inspection.
                                     • We need 4 K atoms on the left, and 4 H
                                       atoms on the right.




                                     • The final balanced equation is

                                     2K2Cr2O7 + 2H2O + 3S        3SO2 + 4KOH + 2Cr2O3
Chemistry 40S                                                  Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Half-Reactions Method
  Redox                              • Half-reactions, as their name suggests, show the
  Reactions                            oxidation or reduction reaction.
                                     • For example:
                                            Cu(s) + 2AgNO3(aq) Cu(NO3)2(aq) + 2Ag(s)
                                     • The oxidation half reaction shows the oxidation of
                                       copper to copper (II) ions and the loss of electrons:
                                                       Cu(s) Cu2+(aq) + 2e¯
                                     • The loss of electrons is indicated in the equation by
                                       putting electrons on the product side of the
                                       equation.
                                     • The reduction half reaction shows the reduction of
                                       silver ions to metallic silver and the gaining of
                                       electrons:
                                                       Ag+ (aq) + 1e¯    Ag (s)
                                     • Gaining electrons is indicated in the equation by
                                       placing electrons on the reactant side of the
                                       equation.
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Half-Reactions Method
  Redox                              • Redox reactions often occur in the
  Reactions                            presence of acids or bases. The half-
                                       reaction method is the preferred
                                       method for balancing these types of
                                       reactions.
                                     • In general, the method requires the
                                       entire equation to be separated into
                                       the oxidation and reduction half-
                                       reactions. The electrons are balanced
                                       and the overall balanced equation is
                                       produced by adding the two balanced
                                       half-reactions.
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions



  Balancing                          Half-Reactions Method
  Redox                              • Steps for Balancing Redox Reactions in
  Reactions                            Acidic Solutions
                                     • This method will be demonstrated by
                                       balancing the following reaction in an acidic
                                       solution.
                                         Cr2O72¯(aq) + SO3 2¯(aq) Cr3+(aq) + SO42-(aq)
                                     • Step 1: Assign oxidation numbers. Identify
                                       then write the oxidation and reduction half-
                                       reactions.
                                     • Step 2: Balance all elements except hydrogen
                                       and oxygen. Add electrons lost and gained.
                                     • Step 3: Balance oxygen atoms by using H2O.
                                     • Step 4: Balance hydrogen atoms using H+
                                       ions.
                                     • Step 5: Balance the number of electrons lost
                                       and gained.
                                     • Step 6: Add the two half-reactions.
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions


                                     Half-Reactions Method
  Balancing
  Redox                              • The first part of balancing redox
  Reactions                            reactions in basic solutions follows the
                                       same steps as that for acidic
                                       solutions. Before adding the two half-
                                       reactions, you add the same number
                                       of hydroxide ions as hydrogen ions to
                                       BOTH sides of the equation. We
                                       eliminate the hydrogen ions by
                                       forming water
                                                     (H+ + OH-     H2O)
Chemistry 40S                                                 Unit 3 – Acid/Base
Equilibria1-11
 Outcome
 Balance oxidation-reduction reactions using redox methods.
 Include acidic and basic solutions


                                     Half-Reactions Method
  Balancing
  Redox                              • For example, balance the following
  Reactions                            reaction in a basic solution.
                                           MnO4¯ + C2O42¯          CO2 + MnO2

                                     • Step 1: Assign oxidation numbers.
                                       Identify then write the oxidation and
                                       reduction half-reactions.
                                     • Step 2: Add water and hydrogen ions to
                                       balance oxygen and hydrogen.
                                     • Step 3: Add hydroxide ions to each side
                                       for each hydrogen ion.
                                     • Step 4: Change the hydroxides and
                                       hydrogens to waters .
                                     • Step 5: Balance electrons lost and
                                       gained .
                                     • Step 6: Add the two half-reactions.

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Chem 40S Uunit 1 Notes

  • 1.
  • 2. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. Solubility & Precipitation Compare and Contrast Solubility vs Precipitation
  • 3. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • When a solute dissolves in a solvent, The the individual particles of the solute Solution separate from the other particles of Process the solute and move between the spaces of the solvent particles. The solvent particles collide with the A Review from solute particles and forces of Chemistry 30S attraction between solute and solvent particles "hold" the solute particles in the spaces. • For a solute to be dissolved in a solvent, the attractive forces between the solute and solvent molecules must be greater than the forces of attraction between the solute molecules.
  • 4. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. 1. The solvent particles must move apart to The make room for solute particles. This process requires energy to overcome Solution forces of attraction between solvent Process particles. The first step in the dissolving process is endothermic. A 3 Step 2. The solute particles must separate form the other solute particles. This process Process also requires energy to overcome the forces of attraction between the solute particles. The second step in the dissolving process is endothermic. 3. When the solute particles move between the solvent particles the forces of attraction between solute and solvent take hold and the particles "snap" back and move closer. This process releases energy. The final step in the dissolving process is exothermic.
  • 5. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • The total heat change in the Energy dissolving process is the sum of the Changes three heat changes. If the sum of During the heat absorbed in the first two Dissolving steps of the dissolving process is greater than the heat released in the last step, the dissolving of that substance will be endothermic. If the dissolving process for a substance is endothermic, the container will feel cooler as the substance dissolves. • In some cases, the exothermic process is larger than the sum of the two endothermic processes. In these cases, as the solid dissolves large amounts of heat are evolved.
  • 6. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • When we talk about the mixing of two Solubility or more substances together in solution we must consider solubility. Simply defined, it is a measure of how much solute will dissolve into the solvent. Not all substances will dissolve in all solvents. • Example 1: NaCl(s) dissolved in water Molecular level: NaCl (solid) + H2O (liquid) NaCl(aq)
  • 7. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. Student TASK Solubility • Create a series of drawings that outline what happens in the solution process involving NaCl dissolving in water.
  • 8. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • Example 1: NaCl(s) dissolved in water Solubility Symbolic level: NaCl(s) → NaCl(aq)
  • 9. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • A precipitation reaction is a common Precipitation type of chemical reaction in solution chemistry. Basically, two or more solutions are combined resulting in a reaction that produces an insoluble product, a precipitate. Typically, these types of reactions involve ionic compounds in aqueous solution. The precipitation reaction is said to occur because of the strong attractive forces certain ions have for each other. These ions combine and fall out of solution in the formation of a solid. • The ability to predict precipitate formation is based upon solubility. When the product of a reaction is insoluble, it precipitates.
  • 10. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • Example 1: NaCl(s) and AgNO3 combined together Precipitation Molecular level: •
  • 11. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • Example 1: NaCl(s) and AgNO3 combined together Precipitation Molecular level: •
  • 12. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. Student TASK Precipitation • Create a series of 3 diagrams that outline what happens when NaCl and AgNO3 are combined in a precipitation reaction. Diagram 1 – draw Na+ and Cl- ions circulating amidst the water molecules Diagram 2 – AgNO3 is drawn with the Ag+ and NO3- ions floating around the water molecules Diagram 3 – Shows the mixing of the two solutions. The Ag+ and Cl- combine to form a precipitate.
  • 13. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. Precipitation • Symbolic level: Molecular equation: NaCl (aq) + AgNO3 (aq) → AgCl (s) + NaNO3 (aq) Ionic equation: Na+ (aq) + Cl- (aq) + Ag+ (aq) + NO3- (aq) → AgCl (s) + Na+ (aq) + NO3- (aq) Net ionic equation: Ag+ (aq) + Cl- (aq) → AgCl (s)
  • 14. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. Precipitation • When certain solutions of electrolytes are mixed, the cation of one solute may combine with the anion of the other How to write solute to form an insoluble compound. chemical This leads to the formation of a equations for precipitate. precipitation • A precipitate is an insoluble solid that reactions settles from a solution. For instance, when a solution of Pb(NO3)2 is mixed with a solution of HCl, a precipitate of insoluble PbCl2(s) forms. This occurs because combining the solutions results in a new solution containing more PbCl2(aq) than is soluble. A condition referred to as supersaturation. In this case, solid PbCl2 must settle out of the solution.
  • 15. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. • In the molecular equation the Precipitation formulas of the compounds are written as their usual chemical formulas. Pb(NO3)2 (aq) + 2HCl (aq) PbCl2 (s) + 2HNO3 (aq) • The precipitation reaction is more accurately represented by the ionic equation. The ionic equation shows the compounds as being dissociated in solution. Pb2+ (aq) + 2NO3- (aq) + 2H+ (aq) + 2Cl– (aq) PbCl2 (s) + 2H+ (aq) + 2NO3- (aq)
  • 16. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. Precipitation Pb2+ (aq) + 2NO3- (aq) + 2H+ (aq) + 2Cl– (aq) PbCl2 (s) + 2H+ (aq) + 2NO3- (aq) • If you examine the ionic equation, you will notice that the H+ ions and NO3-ions are not involved in the formation of the precipitate. We refer to the ions which are not involved in the reaction as spectator ions. Identical species on both sides of the equation can be omitted from the equation. The net ionic equation shows only the species that actually undergo a chemical change. Pb2+ (aq) + 2Cl– (aq) PbCl2 (s) • In order to predict whether a precipitate will form when two solutions are mixed, you need to know the solubility rules for ionic compounds.
  • 17. Outcome 1-01 Explain observed examples of solubility and precipitation at the molecular and symbolic levels. Precipitation
  • 18. Outcome 1-02 Perform a lab to develop a set of solubility rules. Outcome 1-03 Use a table of solubility rules to predict the formation of a precipitate. Solubility Rules
  • 19. Outcome 1-02 Perform a lab to develop a set of solubility rules. Outcome 1-03 Use a table of solubility rules to predict the formation of a precipitate. Process Notes for Writing Net Ionic Equations Rules
  • 20. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a strong acid. Acid/Base Definitions of acids and bases Review • Arrhenius acid: generates [H+] in solution base: generates [OH-] in solution • normal Arrhenius equation: acid + base salt + water • example: HCl + NaOH NaCl + H2O
  • 21. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a strong acid. Acid/Base • A strong acid is defined as an Review acid that completely dissociates into ions. This means that if there are 100 molecules of HCl dissolved in water, 100 ions of H+ and 100 ions of Cl- are produced. • It should be stressed that there are only 6 strong acids. These are: – hydrochloric acid (HCl), – hydrobromic acid (HBr), – hydroiodic acid (HI), – sulfuric acid (H2SO4), – nitric acid (HNO3), – perchloric acid (HClO4).
  • 22. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Acid/Base • A strong base is defined as a Review base that completely dissociates into ions. This means that if there are 100 formula units of NaOH dissolved in water, 100 ions of Na+ and 100 ions of OH- are produced. • Strong bases include any ionic compound that contains the hydroxide (OH-) ion. • When combined with the hydroxide ion, elements found in groups 1 and 2 form strong bases.
  • 23. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Naming Acids • To name a binary acid follow the steps given: 1. the prefix "hydro" is used 2. the root of the anion is used 3. the suffix "ic" is used 4. the word "acid" is used as the second word in the name • Example of naming a binary acid: HCl Step 1: hydro- Step 2: -chloride Step 3: -chloric Step 4: hydrochloric acid
  • 24. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Naming Acids • Naming polyatomic acids follow a different set of rules. Many of the oxygen-rich polyatomic negative ions form acids that are named by replacing the suffix -ate with -ic and the suffix -ite with -ous. • To name oxyacids (acids containing the element oxygen) you recognize them by the general formula HaXbOc where X represents an element other than hydrogen or oxygen. If enough H+ ions are added to a (root)ate polyatomic ion to completely neutralize its charge, the (root)ic acid is formed • Examples of polyatomic acids: – If one H+ ion is added to nitrate, NO3- – HNO3 is formed. This is named nitric acid. – If two H+ ions are added to sulfate, SO42- – H2SO4 is formed. This is named sulfuric acid.
  • 25. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Neutralization • Most common acid-base Reactions reactions take place in water solutions (commonly referred to as aqueous solutions). • In the reaction of an acid with a base in aqueous solution, the hydrogen ions of the acid react with the hydroxide ions of the base to give water. The second product is a salt, which is composed of the positive metal ion from the base and the negative ion from the acid. • In general, the reaction for a neutralization reaction is given by acid + base → salt + water
  • 26. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Neutralization • For example, Reactions • HCl(aq) + KOH(aq) → H2O(l) + KCl(aq) • Since HCl(aq) and KOH(aq) are fully ionized in solution, the preceding equation can be written as • H+ (aq) + Cl− (aq) K+(aq) + OH−(aq) → H2O (l) K+(aq) + Cl−(aq) • Ions common to both sides (spectator ions) can be canceled to yield • H+(aq) + OH−(aq) → H2O(l) • This is referred to as the net ionic equation for the neutralization reaction. If H3O+ is substituted for H+ (aq) the neutralization equation becomes • H3O+(aq) + OH−(aq) → 2 H2O (l)
  • 27. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Process Notes for Writing Net Ionic Equations Rules
  • 28. Outcome 1-04 Write balanced neutralization reactions involving strong acids and bases. Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Process Notes for Writing Net Ionic Equations Rules
  • 29. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titrations • A titration is a carefully controlled neutralization reaction. • To perform a titration, a standard solution is required. A standard solution is a solution of a strong acid or base of known concentration. To determine the concentration of an acid, a basic standard solution is required, and vice versa for an unknown base. The standard solution is usually added to a sample of unknown concentration, until neutralization has occurred.
  • 30. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titrations • A buret is used to control the additions of acids and bases in a titration. The buret determines the volumes of acids and bases added in a titration. • If you recall, when an acid or base is just neutralized, the moles of hydronium ions from the acid and moles of hydroxide ions from the base are equal. The point at which the amount of standard acid or base solution added just neutralizes the unknown sample is called the equivalence point.
  • 31. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titrations • The equivalence point can be determined by adding a pH indicator to the unknown sample or by using a pH meter to measure the pH change as standard solution is added to the sample. If an indicator is used, the point in the titration at which the desired colour forms is called the endpoint of the titration. The indicator is chosen so that the endpoint and the equivalence point are very close. • The endpoint and the equivalence point are NOT the same thing. The equivalence point is a single point defined by the reaction stoichiometry. The endpoint is determined by the choice of indicators.
  • 32. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titrations Titration Procedure • When performing an acid-base titration on an unknown solution, both the standard and unknown solutions are placed into separate burets. For this example, we will determine the concentration of a hydrochloric acid solution using a 0.100 mol/L solution of NaOH. • Each buret is filled and the initial volume readings are taken from the bottom of the meniscus (the smile-shaped surface of the solution in the container). • A sample or aliquot of the acid solution is released into an Erlenmeyer flask. The acid volume in the buret is read and called the "final acid volume". The volume of the aliquot is equal to: final volume reading - initial volume reading
  • 33. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titrations Titration Procedure - continued • We will use phenolphthalein as our indicator. The endpoint will be reached when the sample turns a light pink. Even though phenolphthalein turns pink at a pH of about 8.2, this is not a significant problem, as we will see later. • We slowly add the standard base solution to the flask, with stirring or swirling, until the solution in the flask turns (and stays) a light pink. We take the reading on the base buret and call this the "final base volume". • This procedure is repeated until there are several pieces of consistent data.
  • 34. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titration Procedure
  • 35. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titration Video Demo
  • 36. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Determining Example 1 Concentratio n • A titration was performed using a standard solution of 0.100 mol/L NaOH into and unknown HCl solution. The following data was collected: Base Acid Final Volume Reading 14.45 mL 12.57 mL Initial Volume Reading 0.62 mL 1.13 mL Determine the concentration of the acid.
  • 37. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Determini Example 2 ng the Mass of • A student receives a solid an sample of sulfamic acid (molar unknown mass is 97.09 g/mol), a Sample monoprotic acid, and dissolves the sample in enough water to make 100.0 mL of solution. The students takes a 12.00 mL aliquot and titrates with 0.0985 mol/L sodium hydroxide. If 13.38 mL of the base is needed to reach the endpoint, what is the mass of the sample of acid?
  • 38. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titration • If pH readings are taken during a Curves titration and those pH values are plotted, a titration curve is generated. The general shape of the curves generated may be grouped into families, according to the solution titrated and the titrating solutions. We will discuss four classes of titrations: –1. Strong acid titrated with strong base. –2. Strong base titrated with strong acid. –3. Weak acid titrated with strong base. –4. Weak base titrated with strong acid.
  • 39. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a strong acid. Titration 1. Strong Acid Titrated with a Strong Base Curves
  • 40. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titration 2. Strong Base Titrated with a Strong Acid Curves
  • 41. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titration 3. Titration of a Weak Acid with a Strong Base Curves
  • 42. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titration 4. Titration of a Weak Base with a Strong Acid Curves
  • 43. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong baseand a strong acid. Titration Curves
  • 44. Chemistry 40S Outcome 1-04 Unit 3 – Acid/Base Equilibria neutralization reactions involving strong acids and bases. Write balanced Outcome 1-05 Perform a lab to demonstrate the stoichiometry of a neutralization reaction between a strong base and a strong acid. Titration Curves
  • 45. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation What is oxidation and reduction? Reduction • The term “oxidation” was first applied to the combining of oxygen with other elements (ex. rusting iron or burning carbon or methane). Burning is another name for rapid oxidation. • The term “reduction” originally meant the removal of oxygen from a compound. The term reduction comes from the fact that the free metal has a lower mass than its oxide compound. There is a decrease or reduction in the mass of the material as the oxygen is removed.
  • 46. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation What is oxidation and reduction? Reduction • Chemists recognized that other nonmetallic elements unite with substances in a manner similar to that of oxygen (ex. hydrogen, antimony, and sodium will burn in chlorine; iron will burn in fluorine). • Therefore, the term oxidation was redefined as the process by which electrons are removed from an atom or ion. • Reduction was then defined as the process by which any atom or ion gains electrons.
  • 47. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation Reduction
  • 48. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation What is oxidation and reduction? Reduction • Oxidation occurs when an atom loses one or more electrons and reduction is when an atom gains one or more electrons. There are two mnemonics to help us remember these terms: • "OIL RIG": Oxidation Is Losing electrons, Reduction Is Gaining electrons Or • "LEO says GER": Losing Electrons is Oxidation, Gaining Electrons is Reduction
  • 49. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation- What are REDOX Reactions? Reduction • Oxidation-Reduction reactions, or Reactions Redox reactions, are defined as chemical changes that occur when electrons are transferred from one reactant to another. • For example, 2 Mg(s) + O2(g) → 2 MgO(s) • If this reaction is written in ionic form it becomes: 2 Mg0 + O20 → Mg2+ O2- • Magnesium and oxygen gases are both elements and have no charge • Non-scientists usually refer to this reaction as burning or combustion but as scientists, we refer to this reaction as oxidation.
  • 50. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation- What are REDOX Reactions? Reduction • For example, Reactions 2 Mg(s) + O2(g) → 2 MgO(s) • We say that the magnesium has been oxidized to MgO by the reaction with oxygen gas • Considering the charges, the metal has gone from a 0 charge to 2+ and the non-metal from 0 charge to 2- • In this reaction magnesium begins as a neutral atom and loses two electrons to become a Mg2+ ion in MgO. Magnesium is oxidized. Oxygen begins as a neutral atom and gains the two electrons from magnesium to become an O2-¯ion in MgO. Oxygen is reduced.
  • 51. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation- What are REDOX Reactions? Reduction • For example, Reactions 2 Mg(s) + O2(g) → 2 MgO(s) • If we look at the change in ion charge as a function of electrons, the following relationships can be written: • 2 Mg → 2Mg 2+ + 4 e- in this equation, charge is conserved, 0 charge on both sides • O2 + 4 e- → 2O 2- in this equation, charge is conserved, 4- charge on both sides
  • 52. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation- What are REDOX Reactions? Reduction Reactions • Similarly, the reaction of magnesium combining with chlorine to produce magnesium chloride is also a redox reaction. Mg(s) + Cl2(g) → MgCl2(s) • Magnesium loses two electrons to become a Mg2+ ion and is oxidized. Each chlorine atom gains one electron from magnesium to become Cl- ions. Each chlorine atom is reduced.
  • 53. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation- What are REDOX Reactions? Reduction Reactions
  • 54. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidation- What are REDOX Reactions? Reduction Reactions
  • 55. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Reducing What are Reducing Agents? Agents
  • 56. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Oxidizing What are Oxidizing Agents? Agents
  • 57. Chemistry 40S Unit 3 – Acid/Base Equilibria1-08 Outcome Define oxidation and reduction. Include: gain and loss of electrons, oxidizing agent, reducing agent. Reducing What are Reducing & Oxidizing & Agents? Oxidizing Agents • Any substance which causes the reduction of another substance is called the reducing agent. • Any substance which causes the oxidation of another substance is called an oxidizing agent. 2 Mg(s) + O2(g) → 2 MgO(s)
  • 58. Chemistry 40S Unit 3 – Acid/Base Equilibria1-09 Outcome Determine the oxidation numbers for atoms in compounds and ions. Oxidation Assigning Oxidation Numbers Numbers • The oxidation number represents the charge the atom would have if every bond were ionic. Not every bond is ionic, but chemists assume they are for this system. The oxidation number is not always the actual charge, but it is very helpful to follow electrons in redox reactions.
  • 59. Chemistry 40S Unit 3 – Acid/Base Equilibria1-09 Outcome Determine the oxidation numbers for atoms in compounds and ions. Oxidation Assigning Oxidation Numbers Numbers – Oxidation numbers are always assigned PER ATOM. – The oxidation numbers of all uncombined elements is zero. (ex. O2, K(s), H2, – The oxidation number of monatomic ions equals the charge of that ion. – In compounds, the oxidation number for alkali metals (ex. Li, Na, K, etc.) is always +1. – In compounds, the oxidation number for the alkaline earth metals (ex. Be, Mg, Ca, etc.) is always +2. – In compounds, the oxidation number of aluminum is always +3.
  • 60. Chemistry 40S Unit 3 – Acid/Base Equilibria1-09 Outcome Determine the oxidation numbers for atoms in compounds and ions. Oxidation Assigning Oxidation Numbers Numbers – In compounds, the oxidation number of fluorine is -1. – In compounds, the oxidation number of hydrogen is +1. An exception is in metal hydrides, such as NaH or MgH2, when hydrogen is -1. – In compounds, the oxidation number of oxygen is -2. An exception is in peroxides, such as H2O2 or Na2O2, when its oxidation number is -1. – For any neutral compound, the sum of the oxidation numbers for each atom must be zero. – For a poly atomic ion, the sum of the oxidation numbers for each atom must be the charge of that ion. Note the difference between ion charge and oxidation numbers: for example, the magnesium ion, Mg 2+ ion charge = 2+ oxidation number = +2
  • 61. Chemistry 40S Unit 3 – Acid/Base Equilibria1-10 Outcome Identify and describe reactions as redox or non-redox. Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance Redox Recognizing Redox Reactions Reactions • In order to recognize a redox reaction, we must follow the electrons. We can follow the electrons by determining if the oxidation numbers change. If no oxidation numbers change, the reaction is NOT a redox reaction.
  • 62. Chemistry 40S Unit 3 – Acid/Base Equilibria1-10 Outcome Identify and describe reactions as redox or non-redox. Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance Redox Recognizing Redox Reactions Reactions Example – Is the reaction below a redox reaction? SO2 + H2O → H2SO3 Solution – If we assign oxidation numbers to each atom, we find – the oxidation number of S remains at +4 in the reactants and in the products, – O remains unchanged in the products at -2 and H remains unchanged at +1. – The oxidation numbers do not change, so electrons were not transferred. Therefore, this is not a redox reaction.
  • 63. Chemistry 40S Unit 3 – Acid/Base Equilibria1-10 Outcome Identify and describe reactions as redox or non-redox. Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance Redox Recognizing Redox Reactions Reactions Example – Is the reaction below a redox reaction? Cu(s) + 2AgNO3(aq) → Cu(NO3)2(aq) + 2 Ag(s) Solution – Assign oxidation numbers to each atom, – Cu is zero in the reactants and +2 in the products. – Ag is +1 in the reactants and zero in the products. – N = +5 in both products and reactants. – O = -2 in both products and reactants.
  • 64. Chemistry 40S Unit 3 – Acid/Base Equilibria1-10 Outcome Identify and describe reactions as redox or non-redox. Include: oxidizing agent, reducing agent, oxidzed substance, and reduced substance Redox Recognizing Redox Reactions Reactions Example – Is the reaction below a redox reaction? Cu(s) + 2AgNO3(aq) → Cu(NO3)2(aq) + 2 Ag(s) Solution – This is redox reaction, since the oxidation numbers of Cu and Ag change. – Cu is oxidized because its oxidation number becomes more positive, indicating it has lost electrons. . – The oxidation number of Ag becomes more negative, indicating a gain of electrons. Ag is reduced.
  • 65. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Balancing Redox Reactions Redox Reactions • Redox reactions transfer electrons from one substance to another. Balancing a redox reaction balances the number of electrons lost and gained, then ensures the reaction obeys the Law of Conservation of Mass. • There are two methods we will use to balance redox reactions: – Oxidation Number Method – Half-Reactions Method
  • 66. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Oxidation Number Method Redox Reactions • We will learn this method by balancing the following reaction: K2Cr2O7 + H2O + S SO2 + KOH + Cr2O3 • Step 1: Assign oxidation numbers. • Eventually, you will be able to recognize those just substances that are oxidized and reduced. You can just label those substances.
  • 67. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Oxidation Number Method Redox K2Cr2O7 + H2O + S SO2 + KOH + Cr2O3 Reactions • Step 2: Identify substances oxidized and reduced, then balance electrons lost and gained. • S is oxidized and Cr is reduced. • Notice that there are two Cr atoms and each gains three electrons, for a total of six.
  • 68. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Oxidation Number Method Redox K2Cr2O7 + H2O + S SO2 + KOH + Cr2O3 Reactions • Step 2 (continued): We then determine the lowest common multiple of 6 and 4, which is 12. We multiply the S atoms by 3 and the Cr atoms by 2, so the total number of electrons lost and gained is 12.
  • 69. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Oxidation Number Method Redox K2Cr2O7 + H2O + S SO2 + KOH + Cr2O3 Reactions • Step 3: Balance all other atoms by inspection. • We need 4 K atoms on the left, and 4 H atoms on the right. • The final balanced equation is 2K2Cr2O7 + 2H2O + 3S 3SO2 + 4KOH + 2Cr2O3
  • 70. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Half-Reactions Method Redox • Half-reactions, as their name suggests, show the Reactions oxidation or reduction reaction. • For example: Cu(s) + 2AgNO3(aq) Cu(NO3)2(aq) + 2Ag(s) • The oxidation half reaction shows the oxidation of copper to copper (II) ions and the loss of electrons: Cu(s) Cu2+(aq) + 2e¯ • The loss of electrons is indicated in the equation by putting electrons on the product side of the equation. • The reduction half reaction shows the reduction of silver ions to metallic silver and the gaining of electrons: Ag+ (aq) + 1e¯ Ag (s) • Gaining electrons is indicated in the equation by placing electrons on the reactant side of the equation.
  • 71. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Half-Reactions Method Redox • Redox reactions often occur in the Reactions presence of acids or bases. The half- reaction method is the preferred method for balancing these types of reactions. • In general, the method requires the entire equation to be separated into the oxidation and reduction half- reactions. The electrons are balanced and the overall balanced equation is produced by adding the two balanced half-reactions.
  • 72. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Balancing Half-Reactions Method Redox • Steps for Balancing Redox Reactions in Reactions Acidic Solutions • This method will be demonstrated by balancing the following reaction in an acidic solution. Cr2O72¯(aq) + SO3 2¯(aq) Cr3+(aq) + SO42-(aq) • Step 1: Assign oxidation numbers. Identify then write the oxidation and reduction half- reactions. • Step 2: Balance all elements except hydrogen and oxygen. Add electrons lost and gained. • Step 3: Balance oxygen atoms by using H2O. • Step 4: Balance hydrogen atoms using H+ ions. • Step 5: Balance the number of electrons lost and gained. • Step 6: Add the two half-reactions.
  • 73. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Half-Reactions Method Balancing Redox • The first part of balancing redox Reactions reactions in basic solutions follows the same steps as that for acidic solutions. Before adding the two half- reactions, you add the same number of hydroxide ions as hydrogen ions to BOTH sides of the equation. We eliminate the hydrogen ions by forming water (H+ + OH- H2O)
  • 74. Chemistry 40S Unit 3 – Acid/Base Equilibria1-11 Outcome Balance oxidation-reduction reactions using redox methods. Include acidic and basic solutions Half-Reactions Method Balancing Redox • For example, balance the following Reactions reaction in a basic solution. MnO4¯ + C2O42¯ CO2 + MnO2 • Step 1: Assign oxidation numbers. Identify then write the oxidation and reduction half-reactions. • Step 2: Add water and hydrogen ions to balance oxygen and hydrogen. • Step 3: Add hydroxide ions to each side for each hydrogen ion. • Step 4: Change the hydroxides and hydrogens to waters . • Step 5: Balance electrons lost and gained . • Step 6: Add the two half-reactions.

Notas do Editor

  1. In this example, 25.0 mL of an HCl solution is titrated with a 0.100 mol/L solution of NaOH. The equation for this reaction is as follows: HCl( aq ) + NaOH( aq )  NaCl( aq ) + H 2 O( l ) At equivalence, the hydronium ion and hydroxide ion concentrations are equal; as are the sodium and chloride ion concentrations. Since sodium ions are a weaker acid than water and chloride ions are a weaker base than water, the solution is neutral. That is, at 25°C the pH will be 7.0. The expected titration curve is shown above. The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L NaOH, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [HCl] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L HCl The pink on the graph indicates the colour change of phenolphthalein with pH change. Despite the colour change at a pH higher than equivalence, the difference is not significant, because the curve is so steep at the equivalence point.
  2. This is very similar to the previous example except, a 25.0 mL sample of strong base, NaOH, is added to the flask and 0.100 mol/L HCl is slowly added from a burette. The curve for this reaction is shown above. Once again, the equivalence volume is at 25.0 mL so the concentration of the NaOH and HCl must be equal at 0.100 mol/L. For both the strong acid with strong base and strong base with strong acid titrations, phenolphtalein (pH range = 8.0 - 9.8), phenol red (pH range = 6.8 - 8.4) or bromothymol blue (pH range = 6.0 - 7.6) would be suitable indicators.
  3. In this example, 25.0 mL of an acetic acid solution is titrated with a 0.100 mol/L solution of NaOH. The equation for this reaction is as follows: HC 2 H 3 O 2 ( aq ) + NaOH( aq ) NaC 2 H 3 O 2 ( aq ) + H 2 O( l ) At equivalence, the [HC 2 H 3 O 2 ] = [OH¯]; [Na + ] = [C 2 H 3 O 2 ¯]; and since sodium ions are a weaker acid than water while C 2 H 3 O 2 ¯ ions are a stronger base than water, the solution will be basic. That is, at 25°C the pH will be greater than 7.0. The expected titration curve is shown above. The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L NaOH, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [HC 2 H 3 O 2 ] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L HC 2 H 3 O 2 The pink on the graph indicates the colour change of phenolphthalein with pH change. Phenolphthalein would be a suitable indicator for this titration. At the half-equivalence volume ( 0.5 V eq ) , half the acid is neutralized, so [HC 2 H 3 O 2 ] = [C 2 H 3 O 2 ¯]. If this is the case, according to the equilibrium law for acetic acid K a = [H 3 O + ]; therefore, pH = pK a (pK a = -logK a ) at half-equivalence volume. A titration curve can be used to find the kA of a weak acid.
  4. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  5. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  6. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  7. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  8. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  9. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  10. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  11. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  12. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  13. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  14. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  15. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  16. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  17. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  18. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  19. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  20. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  21. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  22. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  23. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  24. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  25. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  26. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  27. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  28. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  29. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  30. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  31. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  32. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  33. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  34. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  35. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).
  36. This is very similar to the weak acid/strong base titration, except that the acid is added to the base. In this example, 25.0 mL of an aqueous ammonia solution is titrated with a 0.100 mol/L HCl solution. The equation for the reaction is: HC l ( aq ) + NH 3 ( aq ) NH 4 Cl( aq ) The titration curve appears below: The equivalence point is found in the centre of the steepest portion of the curve, or where the curve appears to change directions. The equivalence volume is 25.0 mL of 0.100 mol/L HCl, since the acid:base stoichiometry is 1:1, moles H + = moles OH¯ = (0.100 mol/L)(0.025 L) = 0.0025 moles [NH 3 (aq)] = 0.0025 moles ÷ 0.025 L = 0.100 mol/L NH 3 (aq) At the half-equivalence volume, [NH 4 + ]=[NH 3 ], and [H 3 O + ]=K a for the conjugate acid NH 4 + . If K a = K W /K b , then at half equivalence volume, pH = pK W - pK b Phenolphthalein would not be a suitable indicator for this reaction, since the equivalence point is at a pH of about 5.3. Suitable indicators would be methyl red (pH range = 4.8 - 6.0) or bromocresol green (pH range = 3.6 - 5.2).