Which of the following statements is correct regarding nucleophilic acyl substitution?
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Correct Answer: E. Addition of a nucleophile to the carbonyl is followed by loss of the leaving group.
Carbonyl compounds react with nucleophiles via an addition mechanism: the nucleophile attacks the carbonyl carbon, forming a tetrahedral intermediate. The tetrahedral intermediate itself can be an alcohol or alkoxide, depending on the pH of the reaction. The tetrahedral intermediate of an acyl compound contains a substituent attached to the central carbon that can act as a leaving group. After the tetrahedral intermediate forms, it collapses, recreating the carbonyl C=O bond and ejecting the leaving group in an elimination reaction. In nucleophilic acyl substitution, the leaving group is ejected in a separate exothermic step. The Hammond Postulate predicts that the transition state for this step resembles the tetrahedral intermediate. Therefore, in the transition state for this step minimal bond breaking has occurred, and the importance of the nature of the leaving group is diminished.
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