1. 2. CH3 1. tom 2. aqueous H₂SO4 a Proton transfer b = Lewis acid/base c = Radical chain substitution HBr CH₂ d = Radical chain addition e = Electrophilic addition f = E1 Elimination 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.
-CH3
1.
tom
2.
OH +
aqueous H₂SO4
a Proton transfer
=
b = Lewis acid/base
c = Radical chain substitution
HBr
OH
CH3
ti
Br
d = Radical chain addition
e = Electrophilic addition
f = E1 Elimination
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. -CH3 1. tom 2. OH + aqueous H₂SO4 a Proton transfer = b = Lewis acid/base c = Radical chain substitution HBr OH CH3 ti Br d = Radical chain addition e = Electrophilic addition f = E1 Elimination 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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