H,SO4 1. H20 n-Bu 2. Na NH2 CN 2 Br NaBr NH3 toluene, reflux n-Bu a = Proton transfer d = Radical chain addition g= E2 Elimination b = Lewis acid/base e = Electrophilic addition h = Syl Nucleophilic substitution c = Radical chain substitution f=El 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.
H,SO4 1. H20 n-Bu 2. Na NH2 CN 2 Br NaBr NH3 toluene, reflux n-Bu a = Proton transfer d = Radical chain addition g= E2 Elimination b = Lewis acid/base e = Electrophilic addition h = Syl Nucleophilic substitution c = Radical chain substitution f=El 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.
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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