7. Substitution Reactions
SN1 Reaction
Problem 6e
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. b.
![](/channels/images/assetPage/verifiedSolution.png)
This video solution was recommended by our tutors as helpful for the problem above
Video duration:
10mPlay a video:
446
views
Was this helpful?