Trifluoroiodomethane undergoes an addition to alkenes in the presence of light by a free-radical chain mechanism. The

Question:

Trifluoroiodomethane undergoes an addition to alkenes in the presence of light by a free-radical chain mechanism. CHCHCHCH=CH + CF3I light CHCHCHCH-CH-CF3 I

The initiation step of this reaction is the light-induced homolysis of the C—I bond: F3C light F3C + I

Using the fishhook notation, write the propagation steps of a free-radical chain mechanism for this reaction.

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Organic Chemistry

ISBN: 9781936221349

6th Edition

Authors: Marc Loudon, Jim Parise

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Question Posted: Nov 26, 2023 12:08 AM

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Trifluoroiodomethane undergoes an addition to alkenes in the presence of light by a free-radical chain mechanism. The

Question:

CH₂CH₂CH₂CH=CH₂ + CF3I light CH3CH₂CH₂CH-CH₂-CF3 I

Step by Step Answer:

Because the CF 3 group has added to the carbon of the double bo...View the full answer

Organic Chemistry

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