1. NaOH HBr H20 Br 2. Ph Ethanol H3C. -Ph КОн Ph KCI H20 H. CI a = Proton transfer d = Radical chain addition g= E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution c = Radical chain substitution f=E1 Elimination i = Sn2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers.

1. NaOH HBr H20 Br 2. Ph Ethanol H3C. -Ph КОн Ph KCI H20 H. CI a = Proton transfer d = Radical chain addition g= E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution c = Radical chain substitution f=E1 Elimination i = Sn2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers.

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

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.21P

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What are the species type of I and II (nucleophile or electrophile)?
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