Worksheet 6.1 Nucleophilic substitutions (SN1 and SN2) 1. In a typical SN2 substitution reaction, a nucleophile (Nuc-) reacts with an alkyl halide that contains a leaving group (X-) in a one-step process. a) Label nucleophile, alkyl halide and leaving group in each of the following reactions b) What bond is formed in this reactions and what bond is broken? Show curly arrow to show mechanism in each case. H3C CH2 H3C-CH2 CI :: Na H3 H₂C-Br CH2 Alhy Halide NaCN NC 0-CH2 CH3 + CH2 + NaBr CH2 CH₂ S Nat + H3C + NaBr Br H₂C-CH3 NaCl Ly
Worksheet 6.1 Nucleophilic substitutions (SN1 and SN2) 1. In a typical SN2 substitution reaction, a nucleophile (Nuc-) reacts with an alkyl halide that contains a leaving group (X-) in a one-step process. a) Label nucleophile, alkyl halide and leaving group in each of the following reactions b) What bond is formed in this reactions and what bond is broken? Show curly arrow to show mechanism in each case. H3C CH2 H3C-CH2 CI :: Na H3 H₂C-Br CH2 Alhy Halide NaCN NC 0-CH2 CH3 + CH2 + NaBr CH2 CH₂ S Nat + H3C + NaBr Br H₂C-CH3 NaCl Ly
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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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Transcribed Image Text:Worksheet 6.1
Nucleophilic substitutions (SN1 and SN2)
1. In a typical SN2 substitution reaction, a nucleophile (Nuc-) reacts with an alkyl
halide that contains a leaving group (X-) in a one-step process.
a) Label nucleophile, alkyl halide and leaving group in each of the following
reactions
b) What bond is formed in this reactions and what bond is broken? Show curly
arrow to show mechanism in each case.
H3C CH2
H3C-CH2
CI
:: Na
H3
H₂C-Br
CH2
Alhy
Halide
NaCN
NC
0-CH2
CH3
+
CH2
+ NaBr
CH2
CH₂
S Nat + H3C
+ NaBr
Br
H₂C-CH3
NaCl
Ly
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