Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
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Chapter 7, Problem 7.13YT
Interpretation Introduction

Interpretation:

The curved arrow notation for the carbocation rearrangement shown is to be supplied.

Concept introduction:

Carbocation rearrangement involves the movement of a hydrogen atom or a methyl group along with their bond pair from an adjacent carbon to the carbon with positive charge. This is possible if it leads to a more stable carbocation. The order of stability of carbocations is 1o < 2o < 3o.

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Problem: Consider the addition of HCI shown below. (a) Draw the arrows for the first step of the mechanism, and show all possible carbocation intermediates. (b) Identify the most stable carbocation intermediate and explain your reasoning. (c) Draw the arrows for the second step of the mechanism, and give the expected major product(s). Pay attention to stereochemistry. Br HCI
Please explain in detail, thank you!
CO2 Follow the curved arrows and draw the product of this reaction. You do not have to consider stereochemistry.

Chapter 7 Solutions

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)

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