Carbohydrates are hydrated carbons; general formula is CH_2O
Three main groups:
Monosaccharides (Single sugars, monomers)
Disaccharides (Double sugars, bond of two monosaccharides)
Polysaccharides (Polymers of monosaccharides)
Describe physical properties of key carbohydrates
Mono- and disaccharides:
Small molecules
Simple sugars
water-soluble (polar; -OH groups)
Crystalline
Taste sweet (e.g. sugar)
Polysaccharides:
Macromolecules (large)
Polymers
Insoluble in water
Do not taste sweet (e.g. flour)
Glucose
Hexose sugar; six-membered structure
Formula: C_6H_12O_6
To count carbon, find oxygen, then count going clockwise
OH is hydroxyl group
In ring structure and straight form in solution, equilibrium between them, but ring is predominant
Glucose Diagram
Label
A) CH_2OH
B) O
C) H
D) OH
E) OH
F) H
G) H
H) OH
I) OH
J) H
K) H
Monosaccharide
Monomers of single sugar unit
General formula is (CH_2O)n
Sub-grouped according to their carbon atoms
Suffix-ose is used in naming, mostly
-OH group is a hydroxyl group (polar, reason for water-solubility)
In straight-chain form, all but 1 C has attached -OH; other has carbonyl group (C=O); ketone or aldehyde, makes them reducing sugars
Benedict’s test: Reducing sugars give positive test; reduce copper (II)sulphate to copper (I), change from blue to brick red, green, or orange-brown (depends on sugar concentration)
Monosaccharide types
Hexose:
6 carbon sugar
General Formula: C_6H_12O_6
Glucose (for respiration)
Fructose (in nectar, sweetness attracts pollinators)
Galactose (With glucose, fors lactose, energy source for young animals)
Pentose:
5 carbon sugar
General Formula: C_5H_10O_5
Ribose (In RNA + ATP)
Deoxyribose (In DNA)
Triose:
3 carbon sugar
General Formula: C_3H_6O_3
Isomers
Many chemical bonds in glucose release energy when hydrolysed in respiration (for ATP)
Plants and animals respire alphaglucose, not betaglucose
Structural Isomers:
Slightly different properties
Monosaccharides have same molecular formula but varied structural formulae
Stereoisomers:
Glucose has two; vary slightly structurally (α-glucose and β-glucose) and have different properties
Disaccharides
2 monosaccharides bond (by condensation reaction); forms disaccharide and water molecule
Bond between reacting monosaccharides is glycosidic
General formula: 2(CH_2O)n - H_2O
Can be hydrolysed into monosaccharide monomers by adding water
Maltose and lactose are both reducing, Sucrose is not (carbonyl group lost in glycosidic bond formation)
Gives negative reaction to Benedict's
Test for non-reducing sugars
Boil with dilute hydrochloric acid to hydrolyse sugar to constituent monosaccharides
Neutralise by mixing with sodiumhydroxide
Retest with Benedict's
Disaccharide types
Maltose:
From 2 α-glucose molecule (between carbons 1 and 4; α 1-4glycosidic bond)
Glucose (energy) source in germinating seeds (formed in starch breakdown in seed food store)
Sucrose
Glucose + Fructose
Form sugars transported in green plants (in phloem)
Lactose:
Glucose + Galactose
Milk Sugar, energy source for young mammals
Polysaccharide
Formed when many monosaccharide monomers bond together by condensation