Solved: Iodination of alkanes using iodine (I2) is usually an unfavorable reaction. (See

Chapter 0, Problem 4-57

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Iodination of alkanes using iodine (I2) is usually an unfavorable reaction. (See 4-17, for example.) Tetraiodomethane (CI4) can be used as the iodine source for iodination, in the presence of a free-radical initiator such as hydrogen peroxide. Propose a mechanism (involving mildly exothermic propagation steps) for the following proposed reaction. Calculate the value of for each of the steps in your proposed mechanism.

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