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Principal components of food

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Function maintains the structure and proper functioning of all living ... 4 chiral carbons. 24 = 16 stereoisomers. Glucose. Glucose. Open chain (acyclic form) ... – PowerPoint PPT presentation

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Title: Principal components of food


1
Principal components of food
2
Principal components
  • Proteins
  • Carbohydrates
  • Fats and oils

3
Proteins
  • Function maintains the structure and proper
    functioning of all living organisms.
  • Structure a polymer formed from about 20 amino
    acids by peptide linkage.

4
Some amino acids
5
Peptide linkage
6
Hydrolysis of proteins
  • Breaks the peptide linkages in a protein molecule
  • The composition of the protein molecule may be
    deduced by using paper chromatography

7
Hydrolysis of proteins
8
Past paper questions
  1. 2001 6c
  2. 2001 6d
  3. 2000 7b

9
Carbohydrates
  • Function provide energy
  • Formula Cx H2yOy
  • Monosaccharides C6H12O6 (glucose, fructose)
  • Disaccharide C12H22O11 (sucrose, maltose)
  • Polysaccharides (C6H10O5)n (starch, cellulose)

10
Stereoisomers of C6H12O6
4 chiral carbons 24 16 stereoisomers
11
Glucose
12
Glucose
  • Open chain (acyclic form)
  • Two Ring forms (cyclic form)
  • M.p. 146oC , 150oC
  • Optical rotations
  • 112o , 19o ? 52.7o

13
(No Transcript)
14
Fructose
15
Reducing sugars
16
Reducing sugars
17
Disaccharides
18
Maltose
19
Maltose
20
Sucrose
21
Polysaccharides
  • Carbohydrate polymers
  • Storage polysaccharides
  • Energy storage starch and glycogen
  • Structural polysaccharides
  • Use to provide protective walls to cells -
    cellulose

22
Starch
23
Cellulose
24
Hydrolysis of sucrose
  • Sucrose, like all disaccharides, is hydrolysed by
    dilute mineral acids to two monosaccharides,
    glucose and fructose
  • C12H22O11 H2O ? C6H12O6 C6H12O6
  • The reaction can be effected by enzyme

25
Hydrolysis of starch
  • A solution of starch can be hydrolysed in the
    presence of an enzyme to a disaccharide, maltose.
  • 2(C6H10O5)n nH2O ? nC12H22O11(maltose)
  • It starch is boiled with dilute sulphuric acid,
    it is hydrolyzed to a monosaccharide, glucose.
    (C6H10O5)n nH2O ? nC6H12O6

26
Past paper questions
  1. 2001 7c
  2. 2000 6c
  3. 1998 7b

27
Fats and oils
28
Triglyceride
29
Fatty acids
30
Fatty acid
31
Fatty acid
32
Hardening of vegetable oil
  • Unsaturated oils usually have a lower melting
    point and exist as a liquid.
  • Hydrogenation of some of the CC bonds converts
    to solid fats.
  • E.g. Margarine

33
Hydrolysis of fats and oils
  • Fats and oils are hydrolysed into carboxylic acid
    and glycerol in human body.
  • The substances are then used as fuel, or used in
    building cell membranes and fatty tissues.
  • In laboratory, hydrolysis can be carried out in
    an alkaline medium (i.e. saponification)

34
Iodine value
  • Unsaturated fat is considered desirable in our
    diet.
  • Iodine value is defined as the number of grams of
    iodine that reacts with 100 grams of fats/oils.

35
Fats / Oils Fats / Oils Iodine values
Animal fats Butter 25-30
Animal fats Dripping 35-65
Animal fats Lard 45-65
Vegetable oils Coconut oil 8-10
Cotton seed oil 80-140
Ground-nut oil 85-105
Olive oil 80-90
Almond oil 90-110
Corn oil 115-130
36
Rancidity
  • Rancidity is caused by reactions of fats / oils
    which release foul smelling aldehydes and fatty
    acids.
  • Two types
  • Hydrolytic rancidity
  • Oxidative rancidity

37
Hydrolytic rancidity
  • Occurs as a result of hydrolysis of glyceride
    molecules to glyerol and free carboxylic acids by
    the presence of moisture in the oils.
  • E.g. Frying of chips in oil at high temp.
  • The reaction is speeded up in the presence of
    certain micro-organisms or enzymes.

38
Oxidative rancidity
  • Occurs when fats/oils are exposed to air and
    undergo oxidation.
  • Fats/oils have a high degree of unsaturation are
    more susceptible to oxidation.
  • The oxidation is a free radical mechanism and is
    accelerated by trace metals, light and free
    radical initiators.

39
Past paper questions
  1. 2000 6a
  2. 1999 7d
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