n-Bu Na NH2 1. -CN CN 2 Br NaBr NH3 toluene, reflux n-Bu OH Aqueous acetone 2. H20 HBr optically active racemic d = Radical chain addition g- E2 Elimination h = SN1 Nucleophilic substitution a - Proton transfer b = Lewis acid/base e - Electrophilic addition 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.

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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n-Bu
Na
NH,
1.
-CN
CN
2 Br
NaBr
NH3
toluene, reflux
n-Bu
OH
Aqueous acetone
2.
H,0
HBr
racemic
optically active
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.
Transcribed Image Text:n-Bu Na NH, 1. -CN CN 2 Br NaBr NH3 toluene, reflux n-Bu OH Aqueous acetone 2. H,0 HBr racemic optically active 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.
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