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Cambridge International A Level Biology Revision Guide

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Chapter 2: Biological molecules<br />

The tails of some fatty acids have double bonds between<br />

neighbouring carbon atoms, like this: –C C–. Such fatty<br />

acids are described as unsaturated because they do not<br />

contain the maximum possible amount of hydrogen. They<br />

form unsaturated lipids. Double bonds make fatty acids<br />

and lipids melt more easily – for example, most oils are<br />

unsaturated. If there is more than one double bond, the<br />

fatty acid or lipid is described as polyunsaturated; if there<br />

is only one it is monounsaturated.<br />

Animal lipids are often saturated (no double<br />

bonds) and occur as fats, whereas plant lipids are often<br />

unsaturated and occur as oils, such as olive oil and<br />

sunflower oil.<br />

Alcohols and esters<br />

Alcohols are a series of organic molecules which contain a<br />

hydroxyl group, –OH, attached to a carbon atom. Glycerol<br />

is an alcohol with three hydroxyl groups (Figure 2.12).<br />

The reaction between an acid and an alcohol produces<br />

a chemical known as an ester. The chemical link between<br />

the acid and the alcohol is known as an ester bond or an<br />

ester linkage.<br />

C COOH + HO C C COOC + H 2 O<br />

acid alcohol ester<br />

The –COOH group on the acid reacts with the –OH<br />

group on the alcohol to form the ester bond , –COO− .<br />

This is a condensation reaction because water is formed<br />

as a product. The resulting ester can be converted back to<br />

acid and alcohol by the reverse reaction of adding water, a<br />

reaction known as hydrolysis.<br />

Triglycerides<br />

The most common lipids are triglycerides (Figure 2.13).<br />

These are fats and oils. A glyceride is an ester formed by<br />

a fatty acid combining with the alcohol glycerol. As we<br />

have seen, glycerol has three hydroxyl groups. Each one is<br />

able to undergo a condensation reaction with a fatty acid.<br />

When a triglyceride is made, as shown in Figure 2.12, the<br />

final molecule contains three fatty acids tails and three<br />

ester bonds (‘tri’ means three). The tails can vary in length,<br />

depending on the fatty acids used.<br />

37<br />

H<br />

O<br />

head<br />

H<br />

3 hydrocarbon<br />

tails<br />

O<br />

H<br />

H<br />

C<br />

C<br />

OH<br />

OH<br />

HO<br />

HO<br />

C<br />

O<br />

C<br />

O<br />

condensation<br />

3H 2 O<br />

H C O<br />

H C O<br />

C<br />

O<br />

C<br />

O<br />

H<br />

C<br />

OH<br />

HO<br />

C<br />

H<br />

C<br />

O<br />

C<br />

H<br />

H<br />

glycerol +<br />

3 fatty acid molecules<br />

with hydrocarbon tails<br />

triglyceride<br />

molecule<br />

fatty acid<br />

fatty acid<br />

or, more simply<br />

glycerol<br />

fatty acid<br />

fatty acid<br />

condensation<br />

3H 2 O<br />

glycerol<br />

fatty acid<br />

fatty acid<br />

Key<br />

glycerol<br />

fatty acid<br />

ester bond<br />

Figure 2.12 Formation of a triglyceride from glycerol and three fatty acid molecules.

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