3.3.9
Carboxylic Acids
and Derivatives
Section 3.3.9 covers carboxylic acids and esters (3.3.9.1): acids as weak acids, esterification, the uses of esters, fats and oils, hydrolysis, soap and biodiesel; and acylation (3.3.9.2): acyl chlorides, acid anhydrides and amides, nucleophilic addition–elimination with water, alcohols, ammonia and primary amines, and the manufacture of aspirin.
Revision Notes
4 revision notes, in the order the specification teaches them.
Carboxylic Acids: Structure, Properties and Preparation
Carboxylic acids: structure and naming, hydrogen bonding, boiling point and solubility, and preparation by oxidation, with nitrile hydrolysis as an extension.
Start revisingReactions of Carboxylic Acids
Reactions of carboxylic acids: salts, esterification.
Start revisingAcyl Chlorides and Acid Anhydrides
Acyl chlorides and acid anhydrides: structure, reactions with water, alcohols, ammonia and amines and the addition–elimination mechanism.
Start revisingEsters: Hydrolysis, Fats, Soap and Biodiesel
Esters: naming, formation, acid and alkaline hydrolysis, fats and oils, soap and biodiesel.
Start revisingSummary Map
Download, print and revise the reactions of this topic at a glance.
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Carboxylic Acids Map
AQA A Level Chemistry · 3.3.9 Carboxylic acids and derivatives
Every reaction on one A4 page: reagents, conditions and reaction type for each arrow, colour coded, with the key tests.
Acyl Chlorides Map
AQA A Level Chemistry · 3.3.9 Carboxylic acids and derivatives
Every reaction on one A4 page: reagents, conditions and reaction type for each arrow, colour coded, with the key tests.
Esters Map
AQA A Level Chemistry · 3.3.9 Carboxylic acids and derivatives
Every reaction on one A4 page: reagents, conditions and reaction type for each arrow, colour coded, with the key tests.
Carboxylic Acids and Derivatives Summary Map
AQA A-level Chemistry · 3.3.9 Carboxylic acids and derivatives
The whole section on one A4 page: carboxylic acids, esterification, ester hydrolysis, fats, soap and biodiesel, acyl chlorides, anhydrides and aspirin.
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3.3.9.1
- iii a
know that carboxylic acids react with alcohols in the presence of an acid catalyst to give esters
Revise - iii b
know that alcohols react with carboxylic acids in the presence of an acid catalyst to give esters
Revise - vi a
know that esters can be hydrolysed in acid conditions to form alcohols and carboxylic acids
Revise - vi b
know that esters can be hydrolysed in alkaline conditions to form alcohols and salts of carboxylic acids
Revise - vii
know that vegetable oils and animal fats can be hydrolysed in alkaline conditions to give soap and glycerol
Revise - viii
know that biodiesel is a mixture of methyl esters of long-chain carboxylic acids produced by reacting vegetable oils with methanol in the presence of a catalyst
Revise
3.3.9.2
- ii h
know the nucleophilic addition-elimination reaction of primary amines with acid anhydrides
Revise - iii
know the industrial advantages of ethanoic anhydride over ethanoyl chloride in the manufacture of aspirin
Revise - iv a
outline the mechanism of nucleophilic addition-elimination reactions of acyl chlorides with water
Revise - iv b
outline the mechanism of nucleophilic addition-elimination reactions of acyl chlorides with alcohols
Revise - iv c
outline the mechanism of nucleophilic addition-elimination reactions of acyl chlorides with ammonia
Revise - iv d
outline the mechanism of nucleophilic addition-elimination reactions of acyl chlorides with primary amines
Revise
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