1. Ethanol 2. Ph. Ph KOH Ph- ota. En a осон OH = Proton transfer d Radical chain addition. E2 Elimination. = Lewis acid/base e Electrophilic addition SN1 Nucleophilic substitution = Radical chain substitution f = E1 Elimination i SN2 Nucleophilic substitution dentify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. -CH3 H + KCI HCI H₂O g h

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter10: Organohalides
Section10.SE: Something Extra
Problem 45AP
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1.
CH3
Ph
oto
KOH
O
OH
Ethanol
Ph
Ph-H
-CH₂
+
KCI
H₂O
2.
OCOH
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.
2.
HCI
Transcribed Image Text:1. CH3 Ph oto KOH O OH Ethanol Ph Ph-H -CH₂ + KCI H₂O 2. OCOH 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. 2. HCI
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