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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Question
![1.
2.
Ph
1.
Ph
2
OH
AlBrs
a = Proton transfer
b = Lewis acid/base
c = Radical chain substitution
NMe₂
H₂SO4
Ph
Ph
NMe₂
Tamoxifen
anti (brest) cancer drug
AlBr
J
Ph
Ph
C
d = Radical chain addition
e = Electrophilic addition
f = E1 Elimination
NMе₂
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
iSN2 Nucleophilic substitution](https://content.bartleby.com/qna-images/question/d60261f3-72eb-4b33-bd74-516ec2297ca3/77f8d492-9810-4ef9-bbdb-450e8c5e61dd/yflxfb6_thumbnail.jpeg)
Transcribed Image Text:1.
2.
Ph
1.
Ph
2
OH
AlBrs
a = Proton transfer
b = Lewis acid/base
c = Radical chain substitution
NMe₂
H₂SO4
Ph
Ph
NMe₂
Tamoxifen
anti (brest) cancer drug
AlBr
J
Ph
Ph
C
d = Radical chain addition
e = Electrophilic addition
f = E1 Elimination
NMе₂
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
iSN2 Nucleophilic substitution
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