7. Substitution Reactions
SN1 Reaction
3:04 minutes
Problem 26c
Textbook Question
Textbook QuestionPropose a mechanism involving a hydride shift or an alkyl shift for each solvolysis reaction.
Explain how each rearrangement forms a more stable intermediate.
Hint: Most rearrangements convert 2° (or incipient 1°) carbocations to 3° or resonance-stabilized carbocations.
c. <IMAGE> + CH3C=O(OH) heat—> <IMAGE> + <IMAGE>
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