15.6 Esters: Structures and Names

Esters have the general formula RCOOR′, where R may be a hydrogen atom, an alkyl group, or an aryl group, and R′ may be an alkyl group or an aryl group but not a hydrogen atom. (If it were hydrogen atom, the compound would be a carboxylic acid.) Figure 15.4 “The Structure of Esters” shows models for two common esters.

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Figure 15.4 The Structure of Esters. Esters feature a carbon-to-oxygen double bond that is also singly bonded to a second oxygen atom, which is then joined to an alkyl or an aryl group. The esters shown here are ethyl acetate (a) and methyl butyrate (b).

Esters occur widely in nature. Unlike carboxylic acids, esters generally have pleasant odors and are often responsible for the characteristic fragrances of fruits and flowers. Once a flower or fruit has been chemically analyzed, flavor chemists can attempt to duplicate the natural odor or taste. Both natural and synthetic esters are used in perfumes and as flavoring agents.

Note

Fats and vegetable oils are esters of long-chain fatty acids and glycerol. Esters of phosphoric acid are of the utmost importance to life. (For more information about fats/oils and esters, see Chapter 17 “Lipids”, Section 17.2 “Fats and Oils”, and Section 15.10 “Esters of Phosphoric Acid”, respectively.)

Names of Esters

Although esters are covalent compounds and salts are ionic, esters are named in a manner similar to that used for naming salts. The group name of the alkyl or aryl portion is given first and is followed by the name of the acid portion. In both common and International Union of Pure and Applied Chemistry (IUPAC) nomenclature, the –ic ending of the parent acid is replaced by the suffix –ate (Table 15.3 “Nomenclature of Esters”).

Table 15.3 Nomenclature of Esters
Condensed Structural Formula Common Name IUPAC Name
HCOOCH3 methyl formate methyl methanoate
CH3COOCH3 methyl acetate methyl ethanoate
CH3COOCH2CH3 ethyl acetate ethyl ethanoate
CH3CH2COOCH2CH3 ethyl propionate ethyl propanoate
CH3CH2CH2COOCH(CH3)2 isopropyl butyrate isopropyl butanoate
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 ethyl benzoate ethyl benzoate

Example 5

Give the common and IUPAC names for each compound.

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Skill-Building Exercise

Give the common and IUPAC names for each compound.

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Example 6

Draw the structure for ethyl pentanoate.

Skill-Building Exercise

  1. Draw the structure for phenyl pentanoate.

Concept Review Exercises

  1. From what carboxylic acid and what alcohol can isopropyl hexanoate be made?

  2. From what carboxylic acid and what alcohol can cyclobutyl butyrate be made?

Key Takeaway

  • An ester has an OR group attached to the carbon atom of a carbonyl group.

Exercises

  1. Draw the structure for each compound.

    1. methyl acetate
    2. ethyl pentanoate
    3. phenyl acetate
    4. isopropyl propionate

  2. Draw the structure for each compound.

    1. ethyl hexanoate
    2. ethyl benzoate
    3. phenyl benzoate
    4. ethyl 3-methylhexanoate

  3. Name each compound with both the common name and the IUPAC name.

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  4. Name each compound with both the common name and the IUPAC name.

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