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IGCSE Chemistry: Cambridge 0620 tutoring, Malaysia

Ester – IGCSE Chemistry Definition

IGCSE Chemistry definition of ester: an organic compound formed from an acid and alcohol. Covers naming, formation, uses, and exam tips for Cambridge 0620.

Published by IGCSEChemistry.com.my

Chemistry teaching team: K. S. Tan (15+ years teaching IGCSE Chemistry) and Ms Yash (10+ years teaching IGCSE Chemistry) and Ms Kartini (15+ years teaching IGCSE Chemistry).

Mapped to Cambridge IGCSE Chemistry 0620 (2026–2028). Last updated 2026-08-19.

Esters link the alcohol and carboxylic acid topics and are a favourite for Paper 4 questions. The naming convention, formation equation, and typical uses are all regularly examined.

The 0620 definition

An ester is an organic compound formed by the reaction of a carboxylic acid with an alcohol, with the loss of water. Esters contain the functional group −COO−.

Formation of esters (esterification)

General equation:

Carboxylic acid + alcohol ⇌ ester + water

Example:

CH₃COOH + C₂H₅OH ⇌ CH₃COOC₂H₅ + H₂O

(Ethanoic acid + ethanol → ethyl ethanoate + water)

Conditions: concentrated sulfuric acid catalyst, gentle warming. The reaction is reversible.

Naming esters

The ester name has two parts:

  1. First part: from the alcohol, ending in −yl (methyl, ethyl, propyl)
  2. Second part: from the acid, ending in −anoate (methanoate, ethanoate, propanoate)
AcidAlcoholEster nameFormula
Methanoic acidMethanolMethyl methanoateHCOOCH₃
Ethanoic acidEthanolEthyl ethanoateCH₃COOC₂H₅
Ethanoic acidMethanolMethyl ethanoateCH₃COOCH₃
Propanoic acidEthanolEthyl propanoateC₂H₅COOC₂H₅

Properties and uses of esters

PropertyDetail
SmellSweet, fruity — many artificial flavourings are esters
SolubilitySlightly soluble in water; miscible with organic solvents
VolatilityRelatively volatile (low boiling points)

Uses:

  • Flavourings and fragrances in food and perfumes
  • Solvents for paints, varnishes, and nail polish remover
  • Polyester manufacture (condensation polymerisation of diesters)

Worked exam question

Ethanol reacts with propanoic acid. (a) Name the ester formed. [1] (b) State the catalyst used. [1] (c) State one use of esters. [1]

Mark scheme

(a) Ethyl propanoate [1]

(b) Concentrated sulfuric acid [1]

(c) Flavourings / fragrances / solvents [1]

Common exam mistakes

  • Reversing the ester name — the alcohol part comes first (−yl), the acid part comes second (−anoate). Ethanol + ethanoic acid = ethyl ethanoate, not ethanoyl ethane.
  • Forgetting the catalyst — concentrated sulfuric acid is required for esterification.
  • Confusing ester formation with neutralisation — neutralisation involves inorganic acids and bases; esterification is an organic reaction.

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Frequently asked questions

How are esters formed?

By reacting a carboxylic acid with an alcohol in the presence of a concentrated sulfuric acid catalyst. Water is also produced: acid + alcohol → ester + water.

How do you name an ester?

The first part of the name comes from the alcohol (ending in −yl), the second part comes from the acid (ending in −anoate). For example, ethanol + ethanoic acid → ethyl ethanoate.

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