1. 2. Br 1. + H₂O a = Proton transfer b = Lewis acid/base c = Radical chain substitution 2. NaOH Aqueous acetone OH + OH 앳 H OH + + HBr d = Radical chain addition e = Electrophilic addition f = E1 Elimination Nal Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution

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
Chapter10: Alcohols
Section: Chapter Questions
Problem 10.50P
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1.
2.
Br
1.
+ H₂O
a = Proton transfer
b = Lewis acid/base
c = Radical chain substitution
2.
NaOH
Aqueous acetone
OH
+
OH
앳
H OH
+
+ HBr
d = Radical chain addition
e = Electrophilic addition
f = E1 Elimination
Nal
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers.
g= E2 Elimination
h = SN1 Nucleophilic substitution
i = SN2 Nucleophilic substitution
Transcribed Image Text:1. 2. Br 1. + H₂O a = Proton transfer b = Lewis acid/base c = Radical chain substitution 2. NaOH Aqueous acetone OH + OH 앳 H OH + + HBr d = Radical chain addition e = Electrophilic addition f = E1 Elimination Nal Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution
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