OH 1. H20 HI 2. BH3 0-BH3 f = SN1 Nucleophilic substitution g = SN2 Nucleophilic substitution a = Proton transfer d = El Elimination b = Lewis acid/base e = E2 Elimination c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a g for your answers. 1. 2. Submit Answer Retry Entire Group 8 more group attempts remaining

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
Section16.SE: Something Extra
Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...
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OH
1.
H20
HI
2.
BH3
O-BH3
d = El Elimination
f = SN1 Nucleophilic substitution
a = Proton transfer
e = E2 Elimination
g = SN2 Nucleophilic substitution
b = Lewis acid/base
c = Electrophilic addition
The rections above involve synthesis or reactions of alcohols and ethers.
Identify the mechanism by which they proceed from anmong the mechanisms listed. Use the letters a - g for your answers.
1.
2.
Submit Answer
Retry Entire Group
8 more group attempts remaining
Transcribed Image Text:OH 1. H20 HI 2. BH3 O-BH3 d = El Elimination f = SN1 Nucleophilic substitution a = Proton transfer e = E2 Elimination g = SN2 Nucleophilic substitution b = Lewis acid/base c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from anmong the mechanisms listed. Use the letters a - g for your answers. 1. 2. Submit Answer Retry Entire Group 8 more group attempts remaining
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