1. 2. H₂SO4 oto a Proton transfer b = Lewis acid/base -CH3 Aqueous acetone e = Electrophilic addition f = E1 Elimination g = E2 Elimination + H₂O OH HO- -CH3 h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution j= Electrophilic aromatic substitutic

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter20: Acidity And Pka Of Phenols
Section: Chapter Questions
Problem 11E
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1.
2.
HO
a = Proton transfer
b = Lewis acid/base
1. f
2.
toto.
H₂SO4
Submit Answer
-CH3
Aqueous
acetone
e = Electrophilic addition
f = E1 Elimination
g=E2 Elimination
OH
H₂O
Retry Entire Group 1 more group attempt remaining
K
...OH
=
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your
answers.
+ HO-S
-CH3
h SN1 Nucleophilic substitution
i
SN2 Nucleophilic substitution
j = Electrophilic aromatic substitution
Transcribed Image Text:1. 2. HO a = Proton transfer b = Lewis acid/base 1. f 2. toto. H₂SO4 Submit Answer -CH3 Aqueous acetone e = Electrophilic addition f = E1 Elimination g=E2 Elimination OH H₂O Retry Entire Group 1 more group attempt remaining K ...OH = Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. + HO-S -CH3 h SN1 Nucleophilic substitution i SN2 Nucleophilic substitution j = Electrophilic aromatic substitution
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