In nucleophilic acyl substitution, addition to the carbonyl by a nucleophile is followed by loss of the leaving group. O loss of the leaving group is followed by rearrangement of the carbocation. ester hydrolysis is followed by deprotonation. O protonation of the carbonyl is followed immediately by loss of the leaving grou O an SN2 reaction occurs.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter24: Amines And Heterocycles
Section24.9: Heterocyclic Amines
Problem 22P
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Question 23
In nucleophilic acyl substitution,
O addition to the carbonyl by a nucleophile is followed by loss of the leaving group.
O loss of the leaving group is followed by rearrangement of the carbocation.
O ester hydrolysis is followed by deprotonation.
O protonation of the carbonyl is followed immediately by loss of the leaving grour
O an SN2 reaction occurs.
Transcribed Image Text:Question 23 In nucleophilic acyl substitution, O addition to the carbonyl by a nucleophile is followed by loss of the leaving group. O loss of the leaving group is followed by rearrangement of the carbocation. O ester hydrolysis is followed by deprotonation. O protonation of the carbonyl is followed immediately by loss of the leaving grour O an SN2 reaction occurs.
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