Please draw out the mechanism for the reaction that involves the deprotonation of the acidic hydrogen on the ester followed by nucleophilic attack on the carbonyl carbon to form an enolate intermediate.
Please draw out the mechanism for the reaction that involves the deprotonation of the acidic hydrogen on the ester followed by nucleophilic attack on the carbonyl carbon to form an enolate intermediate.
Chapter17: Alcohols And Phenols
Section17.SE: Something Extra
Problem 71AP: A problem often encountered in the oxidation of primary alcohols to acids is that esters are...
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Please draw out the mechanism for the reaction that involves the deprotonation of the acidic hydrogen on the ester followed by nucleophilic attack on the carbonyl carbon to form an enolate intermediate.
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