(3) HI does not undergo free radical addition with 1-butene, even in the presence of a peroxide. Please provide an explanation by analyzing the propagation steps if the same radical reaction occurred with HI. Besides the bond dissociation enthalpies in the appendix, the following approximate bond dissociate enthalpies might be useful to you: The component of C=C -310 kJ/mol CH3CH₂CH₂CH₂-Br CH3CH₂CH₂CH₂-I -290 kJ/mol (C-Br bond) -235 kJ/mol (C-I bond)

(3) HI does not undergo free radical addition with 1-butene, even in the presence of a peroxide. Please provide an explanation by analyzing the propagation steps if the same radical reaction occurred with HI. Besides the bond dissociation enthalpies in the appendix, the following approximate bond dissociate enthalpies might be useful to you: The component of C=C -310 kJ/mol CH3CH₂CH₂CH₂-Br CH3CH₂CH₂CH₂-I -290 kJ/mol (C-Br bond) -235 kJ/mol (C-I bond)

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.44P

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