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Umesh Kumar
Assistant Professor
Dept. of Pharm. Chemistry
Hygia Institute of Pharmaceutical Education and Research
Contents
 Biomolecules
 Carbohydrates
 Introduction
 Classification
 Chemical nature
What are Biomolecules?
 Every living matter is composed of mainly six elements - carbon,
hydrogen, oxygen, nitrogen, phosphorus and sulfur.
 Other elements may also include in living matter functionalities like-
Ca, K, Na, Cl, Mg, Fe, Cu, Co, l, Zn, F, Mo and Se.
 These elements form molecules with each other and many molecules
form macromolecules with each others.
 These molecules and macromolecules in living matters are termed as
Biomolecules (Chemical entities for life).
CARBOHYDRATES
Introduction
 Carbohydrates are the most abundant biomolecules on earth.
 Carbohydrates are primarily produced by plants and form a very large
group of naturally occurring organic compounds.
 Carbohydrates are the rich source of energy for living organisms.
 Carbohydrates are polyhydroxy aldehydes or ketones, or substances that
yield such compounds on hydrolysis.
 Carbohydrates have empirical formula (CH2O)n ; some also contains
nitrogen, phosphorous, or sulfur.
Classification of Carbohydrates
 There are major size of classes of carbohydrates;
o Monosaccharides,
o Oligosaccharides, and
o Polysaccharides
• The word “saccharide” is derived form the Greek “sakcharon” , meaning
“sugar”.
1. Monosaccharides
 Monosaccharides (Greek : mono-one) are the simplest group of
carbohydrates and are often referred to as simple sugars.
 They have the general formula Cn(H20)n, and they cannot be further
hydrolyzed.
 Monosaccharides are further classified on the basis of number of carbon
atoms present in the molecule. E.g.
2. Oligosaccharides
 Oligosaccharides (Creek: oligo-few) contain 2-1O monosaccharide
molecules which are liberated on hydrolysis.
 Based on the number of monosaccharide units present, the
oligosaccharides are further subdivided to disaccharides, trisaccharides
etc.
a) Disaccharides - Which yield two monosaccharides’ molecules on hydrolysis.
Which have molecular formula is C12H22O11. e.g., Sucrose, maltose etc.
b). Trisaccharides - Which yield three monosaccharides’ molecules on
hydrolysis and have molecular formula is C18H32O16.
c). Tetrasaccharides - Which yield four monosaccharides molecules
on hydrolysis and have molecular formula is C22H42O21
2. Polysaccharides
 Polysacchari6ls (Creek: poly-many) are polymers of monosaccharide units
with high molecular weight (up to a million).
 They are usually tasteless (non-sugars) and form colloids with water.
 The polysaccharides are of two types - homopolysaccharides and
heteropolysaccharide.
Elucidation of chemical nature of carbohydrates
Glucose………
 Glucose is an aldohexose and is also known
as dextrose.
 It is the monomer of many of the larger
carbohydrates, namely starch, cellulose.
 It is probably the most abundant organic
compound on earth.
 On the basis of glucose properties and
structure, we can elucidate the chemical
nature of carbohydrates.
1. Oxidation
 Glucose gets oxidized to six carbon carboxylic acid (gluconic acid) on
reaction with a mild oxidizing agent like bromine water.
 This indicates that the carbonyl group is present as an aldehydic group.
1. Oxidation
 On oxidation with strong oxidizing agents like nitric acid, glucose as well
as gluconic acid both yield a dicarboxylic acid, saccharic acid.
 This indicates the presence of a primary alcoholic (–OH) group in glucose.
2. Reduction
 On the treatment with reducing agents like sodium amalgam, aldehyde or
ketone group reduces to corresponding alcohols.
C
O H
C
C
C
C
CH2OH
HO
H
H
H
H
H
H
H
D-glucose
+ HgNa
Reduction
CH
HO H
C
C
C
C
CH2OH
HO
H
H
H
H
H
H
H
D-sorbitol
3. Acetylation
 Acetylation of glucose with acetic anhydride gives glucose pentaacetate
which confirms the presence of five –OH groups.
4. Dehydration (Molisch Reagent Test)
 on treatment with H2SO4, carbohydrates eliminate 3 molecules of water
and form furfurals.
C
O H
C
C
C
C
CH2OH
HO
H
H
H
H
H
H
H
D-glucose
Conc.
C
O H
C
C
C
C
CH2OH
H
H
Furfural
O
H2SO4
-3H2O
HYGIA GROUP OF INSTITUTIONS
GHAILA ROAD, GAAZIPUR BALRAM,
FAIZULLAHGANJ, LUCKNOW

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L-2 Biomolecules and carbohydrates.pptx

  • 1. Umesh Kumar Assistant Professor Dept. of Pharm. Chemistry Hygia Institute of Pharmaceutical Education and Research
  • 2. Contents  Biomolecules  Carbohydrates  Introduction  Classification  Chemical nature
  • 3. What are Biomolecules?  Every living matter is composed of mainly six elements - carbon, hydrogen, oxygen, nitrogen, phosphorus and sulfur.  Other elements may also include in living matter functionalities like- Ca, K, Na, Cl, Mg, Fe, Cu, Co, l, Zn, F, Mo and Se.  These elements form molecules with each other and many molecules form macromolecules with each others.  These molecules and macromolecules in living matters are termed as Biomolecules (Chemical entities for life).
  • 4.
  • 6. Introduction  Carbohydrates are the most abundant biomolecules on earth.  Carbohydrates are primarily produced by plants and form a very large group of naturally occurring organic compounds.  Carbohydrates are the rich source of energy for living organisms.  Carbohydrates are polyhydroxy aldehydes or ketones, or substances that yield such compounds on hydrolysis.  Carbohydrates have empirical formula (CH2O)n ; some also contains nitrogen, phosphorous, or sulfur.
  • 7. Classification of Carbohydrates  There are major size of classes of carbohydrates; o Monosaccharides, o Oligosaccharides, and o Polysaccharides • The word “saccharide” is derived form the Greek “sakcharon” , meaning “sugar”.
  • 8. 1. Monosaccharides  Monosaccharides (Greek : mono-one) are the simplest group of carbohydrates and are often referred to as simple sugars.  They have the general formula Cn(H20)n, and they cannot be further hydrolyzed.  Monosaccharides are further classified on the basis of number of carbon atoms present in the molecule. E.g.
  • 9.
  • 10. 2. Oligosaccharides  Oligosaccharides (Creek: oligo-few) contain 2-1O monosaccharide molecules which are liberated on hydrolysis.  Based on the number of monosaccharide units present, the oligosaccharides are further subdivided to disaccharides, trisaccharides etc. a) Disaccharides - Which yield two monosaccharides’ molecules on hydrolysis. Which have molecular formula is C12H22O11. e.g., Sucrose, maltose etc.
  • 11. b). Trisaccharides - Which yield three monosaccharides’ molecules on hydrolysis and have molecular formula is C18H32O16. c). Tetrasaccharides - Which yield four monosaccharides molecules on hydrolysis and have molecular formula is C22H42O21
  • 12.
  • 13. 2. Polysaccharides  Polysacchari6ls (Creek: poly-many) are polymers of monosaccharide units with high molecular weight (up to a million).  They are usually tasteless (non-sugars) and form colloids with water.  The polysaccharides are of two types - homopolysaccharides and heteropolysaccharide.
  • 14.
  • 15. Elucidation of chemical nature of carbohydrates Glucose………  Glucose is an aldohexose and is also known as dextrose.  It is the monomer of many of the larger carbohydrates, namely starch, cellulose.  It is probably the most abundant organic compound on earth.  On the basis of glucose properties and structure, we can elucidate the chemical nature of carbohydrates.
  • 16. 1. Oxidation  Glucose gets oxidized to six carbon carboxylic acid (gluconic acid) on reaction with a mild oxidizing agent like bromine water.  This indicates that the carbonyl group is present as an aldehydic group.
  • 17. 1. Oxidation  On oxidation with strong oxidizing agents like nitric acid, glucose as well as gluconic acid both yield a dicarboxylic acid, saccharic acid.  This indicates the presence of a primary alcoholic (–OH) group in glucose.
  • 18. 2. Reduction  On the treatment with reducing agents like sodium amalgam, aldehyde or ketone group reduces to corresponding alcohols. C O H C C C C CH2OH HO H H H H H H H D-glucose + HgNa Reduction CH HO H C C C C CH2OH HO H H H H H H H D-sorbitol
  • 19. 3. Acetylation  Acetylation of glucose with acetic anhydride gives glucose pentaacetate which confirms the presence of five –OH groups.
  • 20. 4. Dehydration (Molisch Reagent Test)  on treatment with H2SO4, carbohydrates eliminate 3 molecules of water and form furfurals. C O H C C C C CH2OH HO H H H H H H H D-glucose Conc. C O H C C C C CH2OH H H Furfural O H2SO4 -3H2O
  • 21. HYGIA GROUP OF INSTITUTIONS GHAILA ROAD, GAAZIPUR BALRAM, FAIZULLAHGANJ, LUCKNOW