H3C Br H3C ĈX CH3 tert-butyl bromide a + b Prelab Question #1 Homework Unanswered Why does tert-butyl bromide (Scheme 1) not participate in SN2 reactions? d OH # 1-propanol Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. Scheme 1. Tertiary alkyl halides do not undergo an SN2 reaction. bromide is not a sufficiently good leaving group с tert-butyl bromide is a nucleophile tert-butyl bromide is too sterically congested for nucleophiles to approach H3C OH H3C CH3 tert-butanol SN2 reactions require 2 nucleophiles to effectively proceed + Br

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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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H3C.
H₂C+
CH3
tert-butyl bromide
a
Br
b
с
Prelab Question #1
Homework Unanswered
d
K
Why does tert-butyl bromide (Scheme 1) not participate in SN2 reactions?
OH
#
1-propanol
Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer.
bromide is not a sufficiently good leaving group
tert-butyl bromide is a nucleophile
Scheme 1. Tertiary alkyl halides do not undergo an SN2 reaction.
tert-butyl bromide is too sterically congested for nucleophiles to approach
H₂C OH
ने
CH3
H₂C
SN2 reactions require 2 nucleophiles to effectively proceed
tert-butanol
K
Br
Transcribed Image Text:H3C. H₂C+ CH3 tert-butyl bromide a Br b с Prelab Question #1 Homework Unanswered d K Why does tert-butyl bromide (Scheme 1) not participate in SN2 reactions? OH # 1-propanol Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. bromide is not a sufficiently good leaving group tert-butyl bromide is a nucleophile Scheme 1. Tertiary alkyl halides do not undergo an SN2 reaction. tert-butyl bromide is too sterically congested for nucleophiles to approach H₂C OH ने CH3 H₂C SN2 reactions require 2 nucleophiles to effectively proceed tert-butanol K Br
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