Biomolecules Flashcards

1
Q

Carbohydrates: definition

A

Carbohydrates are polyhydroxy aldehydes or polyhydroxy ketonesm or large polymeric molecules which on hydrolysis yield polyhydroxy aldehydes and polyhdroxy ketones.

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2
Q

Monosaccharides: Definition

A

Carbohydrates which cannot be decomposed by further hydrolysis to give simpler carbohydrates

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3
Q

Monosaccharides: General formula + examples

A

(CH2O)n
n = 3 - 7

C6H10O6
Glucose, fructose, galactose
C6H10O5: ribose

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4
Q

Oligosaccharides: definition

A

Carbohydrates which upon hydrolysis give a definite number (2-10) of molecules of monosaccharides are called oligosaccharides

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5
Q

Disaccharides

A

Oligosaccharides

Carbohydrates which upon hydrolysis give two units of the same or different monosaccharides.

E.g. C12H22O11
Maltose, sucrose, lactose

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6
Q

Trisaccharides

A

Oligosaccharides

Carbohydrates which upon hydrolysis give three units of the same or different monosaccharides.

E.g. C18H32O16
Raffinose + 2H2O —hydrolysis—> glucose + fructose + galactose

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7
Q

Tetrasaccharide

A

Oligosaccharides

Carbohydrates which upon hydrolysis give four units of the same or different monosaccharides.

E.g. C24H42O21
Stachyrose + 3H2O —hydrolysis—> glucose + fructose + 2(galactose)

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8
Q

Polysaccharides: definition, general formula, examples

A

The carbohydrates which upon hydrolysis give a large number of monosaccharide molecules are called polysaccharides

(C6H10O5)n
where n = 100 - 3000

E.g. starch, cellulose, glycogen

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9
Q

Reducing sugars: Definition + example

A

Carbohydrates which are capable of reducing Tollen’s reagent and Fehling’s solution are called reducing sugars

E.g all monosaccharides and disaccharides except sucrose

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10
Q

Non-reducing sugars

A

Carbohydrates unable to reduce Tollen’s reagent and Fehling’s solution are called non-reducing sugars

E.g. Sucrose

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11
Q

Aldoses

A

Monosaccharides possessing an aldehyde group (-CHO) are called aldoses

Always present on terminal carbon atom

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12
Q

Ketoses

A

Monosaccharides containing a keto group are called ketoses.

In naturally occurring ketoses, the keto group is present on the second carbon atom

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13
Q

D-configuration

A

When the -OH group on the C atom adjacent to CH2OH group lies on the right hand side in the Fischer projection, the monosaccharide has D-configuration

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14
Q

L-configuration

A

When the -OH group on the C atom adjacent to CH2OH group lies on the left hand side in the Fischer projection, the monosaccharide has L-configuration

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15
Q

Structure of glucose

A
  1. Presence of a straight chain of 6 carbon atoms
  2. Presence of carbonyl group (>C=O)
  3. Presence of aldehydic (-CHO) group
  4. Presence of 5 hydroxyl (-OH) groups
  5. Presence of primary alcoholic group
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16
Q

Glucose structure: prove presence of straight chain of 6 carbon atoms

A

HI + heat
glucose -> n-hexane + water

17
Q

Glucose structure: prove presence of carbonyl group

A

rxn w hydroxylamine NH2OH
glucose -> oxime

18
Q

Glucose structure: prove presence of aldehydic group

A

[O] + Br water

Glucose-> Gluconis acid

19
Q

Glucose structure: prove presence of 5 -OH groups

A

acetic anhydride

glucose -> pentaacetate

20
Q

Presence of primary alcoholic group

A

oxidation with nitric acid

glucose -> saccharic acid