Organic Chemistry, Books a la Carte Plus Mastering Chemistry with Pearson eText -- Access Card Package (8th Edition)
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Chapter 12, Problem 33P
Interpretation Introduction

Interpretation:

The possible monochlorination products along with the stereoisomers has to be drawn.

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Radical bromination of cyclohexene using NBS gives 3-bromo-1-cyclohexene. Draw the allylic radical intermediate formed during this reaction, showing both resonance structures
Draw the major product(s) of the reaction of 1-methylcyclohexene with the following reagents, disregarding stereoisomers: 1. NBS/∆/peroxide    2 . Br2/CH2Cl2      3. HBr        4. HBr/peroxideb. For each reaction, show which stereoisomers are obtained.
Draw the four resonance forms of the allylic carbocation intermediates when the alkene below reacts with HBr as shown below.

Chapter 12 Solutions

Organic Chemistry, Books a la Carte Plus Mastering Chemistry with Pearson eText -- Access Card Package (8th Edition)

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