1. 2. CH3 H3C- -Br CH3 1. + a = Proton transfer b = Lewis acid/base c = Radical chain substitution 2. ICI C₂H5 N-C₂H5 C₂H5 d = Radical chain addition e = Electrophilic addition f = E1 Elimination C₂H5 H-N-C₂Hs Br C₂H5 g = E2 Elimination h = Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution

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Chapter1: Chemical Foundations
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1.
2.
CH3
H₂C+B
-Br
CH3
a Proton transfer
b = Lewis acid/base
c = Radical chain substitution
1.
2.
ICI
C₂H5
N-C₂H5
C₂H5
d = Radical chain addition
Electrophilic addition
e =
f = E1 Elimination
C₂H5
+1
H-N-C₂H5 Br
C₂H5
g = E2 Elimination
h
=
SN1 Nucleophilic substitution
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.
Transcribed Image Text:1. 2. CH3 H₂C+B -Br CH3 a Proton transfer b = Lewis acid/base c = Radical chain substitution 1. 2. ICI C₂H5 N-C₂H5 C₂H5 d = Radical chain addition Electrophilic addition e = f = E1 Elimination C₂H5 +1 H-N-C₂H5 Br C₂H5 g = E2 Elimination h = SN1 Nucleophilic substitution 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.
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