H Ph 1. HO A NaOH Ph Br DMSO / H20 2. N-Br ...HO. N-H a = Proton transfer d = Radical chain addition g = E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution %3D %3D 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. 2.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter8: Addition Via Carbocation
Section: Chapter Questions
Problem 18CTQ: The reactants, intermediates, final products, and all curved arrows showing bonds forming...
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H Ph
1.
HO
NaOH
Ph
Br
DMSO / H20
2.
N-Br
..OH
N-H
a = Proton transfer
d = Radical chain addition
E2 Elimination
b = Lewis acid/base
e = Electrophilic addition
h = SN1 Nucleophilic substitution
Radical chain substitution
f=E1 Elimination
i= SN2 Nucleophilic substitution
C =
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.
2.
Transcribed Image Text:H Ph 1. HO NaOH Ph Br DMSO / H20 2. N-Br ..OH N-H a = Proton transfer d = Radical chain addition E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution Radical chain substitution f=E1 Elimination i= SN2 Nucleophilic substitution C = 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. 2.
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