Chemistry, 06.12.2019 00:31 mslamaya11
Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution between an alcohol and a carboxylic acid; this process is called the fischer esterification reaction. because the alcohol oxygen is a poor nucleophile, the carbonyl carbon is made a better electrophile by protonation of the carbonyl oxygen. the steps of the synthesis are all reversible. the reaction is generally driven to completion by using an excess of the liquid alcohol as a solvent, or by distilling off the product as it forms.
draw curved arrows to show the movement of electrons in this step of the mechanism.
Answers: 2
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Sheela and her brother hari were sitting in the living room, watching tv. suddenly hari said that he thinks something is burning in the other room. how did he get the burning smell?
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Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution between an alcohol and...
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