ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
10th Edition
ISBN: 9781259972348
Author: Carey
Publisher: MCG CUSTOM
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Chapter 6.8, Problem 12P
Interpretation Introduction

Interpretation:

It is to be explained that the carbocation intermediate in the hydrolysis of 2-bromo-3-methylbutane rearranges by a hydride shift rather than a methyl shift.

Concept introduction:

The stability order of carbocation is methyl < primary < secondary < tertiary.

The carbocation can be stabilized by rearrangement due to shift of hydride or methyl group of adjacent carbon.

The selection of hydride or methyl group shift depends on the stability of carbocation formed.

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Predict the products of this organic reaction: O N IN A N + H2O + HCI ? Specifically, in the drawing area below draw the skeletal ("line") structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. 田 C + Explanation Check Click and drag to start drawing a structure. C © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center
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