When exposed to a radical initiator, the C-H bond in HCC13 will cleave homolytically and undergo radical addition to alkenes. With this in mind, propose a mechanism for the following reaction: CCB 0 HCC13 peroxides

When exposed to a radical initiator, the C-H bond in HCC13 will cleave homolytically and undergo radical addition to alkenes. With this in mind, propose a mechanism for the following reaction: CCB 0 HCC13 peroxides

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...

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Question

When exposed to a radical initiator, the C-H bond in HCC13 will cleave homolytically and undergo
radical addition to alkenes. With this in mind, propose a mechanism for the following reaction:
CCB
0:
HCC13
peroxides

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