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IUPAC Nomenclature Rules for Esters

By German Fernandez, 5 March, 2024

Rule 1. Esters result from the condensation of acids with alcohols and are named as salts of the acid they derive from. The IUPAC nomenclature changes the -oic ending of the acid to -oate, ending with the name of the alkyl group attached to the oxygen.

Rule 2. Esters are priority groups over amines, alcohols, ketones, aldehydes, nitriles, amides, and acyl halides. These groups are named as substituents with the ester being the functional group.

Rule 3. Carboxylic acids and anhydrides have priority over esters, which are then named as substituents (alkoxycarbonyl......).

Rule 4. When the ester group is attached to a cycle, the cycle is named as the main chain and the ester is named using the -alkyl carboxylate ending.

Book traversal links for Reglas IUPAC de Nomenclatura para Éteres

  • IUPAC Nomenclature Rules for Anhydrides
  • Up
  • IUPAC Nomenclature Rules for Amides

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