AQA · A-Level · Chemistry

    Course version: 7405 · Version from Sept 2016

    Vegetable oils and animal fats can be hydrolysed in alkaline conditions to…

    Full specification wording

    Carboxylic acids and esters (A-level only): Vegetable oils and animal fats can be hydrolysed in alkaline conditions to give soap (salts of long-chain carboxylic acids) and glycerol.

    Saponification is alkaline hydrolysis carried out on a triglyceride.

    Checked against the AQA 7405 specification (opens in a new tab) on .

    • Point 6 of 8
    • 4 key terms

    Study notes

    From the checked teaching notes for this specification point.

    The idea

    Saponification is alkaline hydrolysis carried out on a triglyceride. Three ester links means three moles of sodium hydroxide per mole of fat, and the products are three molecules of a sodium salt of a long-chain carboxylic acid, RCOO⁻Na⁺, plus one molecule of glycerol. That salt is the soap. It works because it has two incompatible ends: a long non-polar hydrocarbon tail, which mixes with grease, and an ionic COO⁻ head, which is attracted to water. Soap molecules surround a grease droplet with their tails inwards and heads outwards, forming a micelle whose charged surface keeps droplets apart so the grease is lifted and suspended. In hard water the calcium and magnesium salts are insoluble, so scum forms instead.

    What earns the marks

    • Three moles of sodium hydroxide reacting per mole of triglyceride.
    • Glycerol, propane-1,2,3-triol, given as the second product.
    • The soap written as the sodium salt of a long-chain carboxylic acid.
    • Describing the hydrocarbon tail as non-polar and the COO⁻ head as attracted to water.

    Common mistakes and how to put them right

    • Giving the free long-chain carboxylic acid rather than its sodium salt as the product of the alkali.

    • Using one mole of sodium hydroxide per triglyceride instead of three.

    • Naming the alcohol product as ethanol rather than glycerol.

    • Saying the hydrocarbon tail dissolves in the water and the head in the grease.

    Exam tips

    • Count the ester links before you balance: three links means three moles of alkali and three moles of soap.
    • When explaining how soap cleans, name the two ends and say what each is attracted to; 'it dissolves grease' alone scores nothing.

    Try the lesson

    The start of the Carboxylic acids and esters (A-level only): Vegetable oils and animal fats can be hydrolysed in alkaline conditions to give soap (salts of long-chain carboxylic acids) and glycerol. lesson, made from checked teaching notes for this specification point.

    Have a go first

    Which two products are formed when a vegetable oil is hydrolysed with hot aqueous sodium hydroxide?

    Listen

    Saponification is alkaline hydrolysis carried out on a triglyceride. Three ester links means three moles of sodium hydroxide per mole of fat, and the products are three molecules of a sodium salt of a long-chain carboxylic acid, RCOO⁻Na⁺, plus one molecule of glycerol. That salt is the soap. It works because it has two incompatible ends: a long non-polar hydrocarbon tail, which mixes with grease, and an ionic COO⁻ head, which is attracted to water. Soap molecules surround a grease droplet with their tails inwards and heads outwards, forming a micelle whose charged surface keeps droplets apart so the grease is lifted and suspended. In hard water the calcium and magnesium salts are insoluble, so scum forms instead. A strong answer earns marks for these points. three moles of sodium hydroxide reacting per mole of triglyceride. glycerol, propane-1,2,3-triol, given as the second product. the soap written as the sodium salt of a long-chain carboxylic acid. describing the hydrocarbon tail as non-polar and the COO⁻ head as attracted to water. Exam tip: Count the ester links before you balance: three links means three moles of alkali and three moles of soap.

    See it

    A top-down flowchart. A triglyceride undergoes alkaline hydrolysis. This uses three moles of sodium hydroxide per mole of triglyceride and gives two products: soap, the sodium salt of a long-chain carboxylic acid, and glycerol, propane-1,2,3-triol. The soap molecule has two parts: a non-polar hydrocarbon tail and an ionic COO⁻ head attracted to water. Both parts lead to the tails pointing inwards around a grease droplet, forming a micelle whose charged surface keeps droplets apart, so the grease is lifted and suspended.
    It shows the alkaline hydrolysis of a triglyceride giving soap and glycerol, and how the two ends of the soap molecule form a micelle that lifts grease.

    Key words

    Say what each word means before you turn the card.

    saponification

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    soap as a salt

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    glycerol

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    hydrophobic tail and ionic head

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    See every definition
    saponification
    Alkaline hydrolysis carried out on a triglyceride, giving soap and glycerol.
    soap as a salt
    The sodium salt of a long-chain carboxylic acid, RCOO⁻Na⁺, produced along with glycerol.
    glycerol
    Propane-1,2,3-triol, given as the second product of the alkaline hydrolysis.
    hydrophobic tail and ionic head
    A non-polar hydrocarbon tail that mixes with grease and an ionic COO⁻ head that is attracted to water.

    Label the diagram

    Some boxes have lost their names. Pick the right name for each number.

    The diagram again, with 3 boxes numbered instead of named. A top-down flowchart. A triglyceride undergoes alkaline hydrolysis. This uses three moles of sodium hydroxide per mole of triglyceride and gives two products: soap, the sodium salt of a long-chain carboxylic acid, and glycerol, propane-1,2,3-triol. The soap molecule has two parts: a non-polar hydrocarbon tail and an ionic COO⁻ head attracted to water. Both parts lead to the tails pointing inwards around a grease droplet, forming a micelle whose charged surface keeps droplets apart, so the grease is lifted and suspended.
    • 1Box 1

    • 2Box 2

    • 3Box 3

    0 of 3 labelled

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