Ester: Difference between revisions
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{{Image|Ethyl Acetate stickfigure.jpg|right|350px|Ethyl acetate, a small ester.}} | |||
In chemistry, an '''ester''' is a chemical compound that contains a carbonyl functionality attached to an alkoxide. | In chemistry, an '''ester''' is a chemical compound that contains a carbonyl functionality (C=O) attached to an alkoxide. This is done by replacing a hydroxyl group (R-OH) of an acid with an alkoxy group (-O-R) from another molecule such as an alcohol. | ||
== ester | ==Applications== | ||
Esters are widely used in the food industry as artificial flavors. Small esters can be used as [[solvent]]s. Another ester, acetylsalicylic acid or [[aspirin]], is used for medicinal purposes<ref name=Wilcox1984>Wilcox, C.F. (1984). ''Experimental Organic Chemistry, Theory and Practice.'' Macmillan. p. 332; ch. 24.</ref>. | |||
==Synthesis== | |||
Esters may be formed through a variety of [[esterification]] reactions, most typically the condensation reaction of a [[carboxylic acid]] and an [[alcohol]]<ref name=McMurry1996>McMurry, J. (1996). ''Organic Chemistry (4th ed.)''. Scarborough, Ontario: Nelson Canada. pp. 222, 639, 803, 814, 816-817, 823-825.</ref>. For instance, the ester ethyl acetate (shown in the figure) can be produced from the condensation reaction between [[acetic acid]] and [[ethanol]]. Another method of ester preparation ([[alcoholysis]]) uses an acid chloride instead of a carboxylic acid. Both methods involve [[nucleophilic acyl substitution]], that is, the replacement of one [[nucleophile]] attached to a [[carbonyl]] group with an [[alkoxide]] - a superior nucleophile<ref name=McMurry1996 />. In alcoholysis, the leaving nucleophile is a [[halide]] rather than a [[hydroxyl]] group. | |||
An alternative process, suitable for the addition of a relatively small molecule to an alcohol<ref name=McMurry1996 />, is the combination of an alcohol and an [[acid anhydride]]. [[Aspirin]] can be produced by such a reaction, between salicylic acid and acetic anhydride. In these reactions a [[carboxylate]] [[ion]] substitutes instead of an [[alkoxide]]. In all of these reactions an [[oxygen]] in the alcohol's hydroxyl group is retained in the ester linkage<ref name=Wilcox1984 />. | |||
==References== | |||
<references/>[[Category:Suggestion Bot Tag]] | |||
Latest revision as of 16:00, 13 August 2024
In chemistry, an ester is a chemical compound that contains a carbonyl functionality (C=O) attached to an alkoxide. This is done by replacing a hydroxyl group (R-OH) of an acid with an alkoxy group (-O-R) from another molecule such as an alcohol.
Applications
Esters are widely used in the food industry as artificial flavors. Small esters can be used as solvents. Another ester, acetylsalicylic acid or aspirin, is used for medicinal purposes[1].
Synthesis
Esters may be formed through a variety of esterification reactions, most typically the condensation reaction of a carboxylic acid and an alcohol[2]. For instance, the ester ethyl acetate (shown in the figure) can be produced from the condensation reaction between acetic acid and ethanol. Another method of ester preparation (alcoholysis) uses an acid chloride instead of a carboxylic acid. Both methods involve nucleophilic acyl substitution, that is, the replacement of one nucleophile attached to a carbonyl group with an alkoxide - a superior nucleophile[2]. In alcoholysis, the leaving nucleophile is a halide rather than a hydroxyl group.
An alternative process, suitable for the addition of a relatively small molecule to an alcohol[2], is the combination of an alcohol and an acid anhydride. Aspirin can be produced by such a reaction, between salicylic acid and acetic anhydride. In these reactions a carboxylate ion substitutes instead of an alkoxide. In all of these reactions an oxygen in the alcohol's hydroxyl group is retained in the ester linkage[1].