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3-Bromocyclohexene is a secondary halide, and benzyl

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr ISBN: 9780321768414 33

Solution for problem 24P Chapter 6

Organic Chemistry | 8th Edition

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Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Organic Chemistry | 8th Edition

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Problem 24P

3-Bromocyclohexene is a secondary halide, and benzyl bromide is a primary halide. Bothhalides undergo SN1 substitution about as fast as most tertiary halides. Use resonance structures to explain this enhanced reactivity.

Step-by-Step Solution:

Answer :

Step 1</p>

When 3-bromo cyclohexene is used for SN1 substitution reaction then initially it forms allylic carbocation .This allylic carbocation is secondary carbocation .But due to resonance structures of allylic carbocation .But due to resonance structures of allylic carbocation .it reacts faster by SN1 substitution reaction .

Step 2 of 2

Chapter 6, Problem 24P is Solved
Textbook: Organic Chemistry
Edition: 8
Author: L.G. Wade Jr
ISBN: 9780321768414

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3-Bromocyclohexene is a secondary halide, and benzyl

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