What are lipids?
Lipids are a group of biomolecules that do not dissolve in water but dissolve in organic solvents such as ether or alcohol. They are made mostly of carbon, hydrogen and a little oxygen.
Jobs of lipids:
- Energy store: 1 g of fat gives about 37 kJ, roughly twice as much as 1 g of sugar.
- Insulation and protection: fat under the skin keeps heat in and cushions organs.
- Cell membranes: made of phospholipids.
- Hormones and vitamins: steroid hormones (like testosterone), vitamin D.
- Waterproofing: wax on leaves and feathers.
Fatty acids: saturated and unsaturated
A fatty acid is a long hydrocarbon chain with a carboxyl group (–COOH) at one end. General formula of a saturated one: CnH2n+1COOH.
- Palmitic acid: C15H31COOH, 16 carbons, saturated.
- Stearic acid: C17H35COOH, 18 carbons, saturated.
- Oleic acid: C17H33COOH, 18 carbons, one C=C double bond, unsaturated.
How to tell them apart in the lab: shake with bromine water (orange). Oleic acid decolourises it, because bromine adds across the C=C bond. Palmitic and stearic acids leave it orange.
Shorthand: 18:1 means 18 carbons and 1 double bond.
Fats and oils: esters of glycerol
A fat (triglyceride) forms when glycerol (propane-1,2,3-triol) reacts with three fatty acids. Each –OH of glycerol and –COOH of an acid join and release one water molecule. The new link is an ester bond, so fats are esters.
glycerol + 3 fatty acids → triglyceride + 3 H2O
Classification:
- By origin: animal fats (butter, lard) and plant oils (sunflower, coconut).
- By state: solid fats (mostly saturated) and liquid oils (mostly unsaturated). Coconut and palm oil are plant fats that are fairly saturated.
Properties: lighter than water, insoluble in water, greasy. Unsaturated oils decolourise bromine water. Hydrogenation adds hydrogen to C=C bonds with a nickel catalyst and turns oil into solid fat (margarine, vanaspati). Hydrolysis splits a fat back into glycerol and fatty acids; with an alkali it gives soap (saponification).
Uses: food and energy, cooking, soap, candles and cosmetics, biodiesel.
Other lipids: phospholipids, steroids, waxes
Saponifiable lipids contain fatty acids joined by ester bonds, so an alkali can turn them into soap: fats/oils (triglycerides), phospholipids, waxes.
- Phospholipids: glycerol + 2 fatty acids + a phosphate group. The head loves water, the tails hate it, so they form a double layer: the cell membrane.
- Waxes: one long fatty acid + one long alcohol. Waterproof coats on leaves and in ears.
Non-saponifiable lipids have no fatty acids, so no soap forms:
- Steroids: four joined carbon rings. Cholesterol (in membranes), sex hormones, vitamin D, bile salts.
- Terpenes: built from isoprene units, for example vitamin A and the pigments that colour carrots (carotenoids).
Try it: solid or liquid?
Put a spoon of ghee or butter and a spoon of cooking oil in two cups in the fridge for an hour. Which one becomes hard first? Predict using the tail shapes, then compare with step 4 and free play in the 3D. (Ask an adult before using the kitchen.)
Key formulas and definitions
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Worked examples
1. How many water molecules are released when one triglyceride forms?
Three: one for each ester bond between glycerol and a fatty acid.
2. A fat is made from glycerol + 3 stearic acids. Will it be solid or liquid at 25 °C?
Solid. Stearic acid is saturated, so the straight tails stack tightly.
3. How can you tell oleic acid from stearic acid?
Add bromine water. Oleic acid (C=C bond) turns it colourless; stearic acid does not.
4. Is cholesterol saponifiable? Why?
No. It is a steroid with no fatty acid or ester bond, so an alkali cannot make soap from it.
Common mistakes
- Saying unsaturated means "has no hydrogen". It means it has fewer H atoms because of C=C double bonds.
- Calling fats polymers. A triglyceride is one molecule made of 4 pieces, not a long repeating chain.
- Thinking all plant oils are unsaturated. Coconut and palm oil are rich in saturated fat.
- Forgetting the 3 water molecules when writing the ester reaction.