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

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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
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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