Organic Chemistry: Principles And Mechanisms
Organic Chemistry: Principles And Mechanisms
2nd Edition
ISBN: 9780393630756
Author: KARTY, Joel
Publisher: W.w. Norton & Company,
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Chapter 12, Problem 12.14P
Interpretation Introduction

Interpretation:

The reagent which can be used for the given transformation is to be determined.

Concept introduction:

The conversion of an alkene to alcohol is carried out by the oxymercuration-reduction reaction. Rearrangement generally does not take place with oxymercuration-reduction because a carbocation intermediate is not formed. The intermediate is a cyclic mercurinium ion.

The product of oxymercuration-reduction follows Markovnikov’s rule. The hydroxyl group (OH) is added to the more substituted carbon atom of the initial double bond. The oxymercuration-reduction carried out with Hg(OAc)2, H2O/THF followed by a reduction using NaBH4, ethanol respectively.

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In the acid-catalyzed aromatic alkylation involving 1-methylcyclohexene and benzene, two isomeric products are possible, but only one is formed, as shown here. Draw the complete mechanism that leads to each product, and explain why only one isomer is formed.
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PROBLEM How might you carry out the following transformation? More than one 20-12 step is needed. -CH2OH ? -CH2CH2OH

Chapter 12 Solutions

Organic Chemistry: Principles And Mechanisms

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