1. Steric hindrance is the unfavorable electron-electron repulsion that results when bonds are forced too close to each other. a. Draw the SN2 mechanism using curved arrows for the reaction of bromoethane with Nu:. asi2 b. Draw the SN2 mechanism using curved arrows for the reaction of 2-bromopropane with Nu:. tipizod c. Given that steric hindrance is unfavorable, predict whether the SN2 reaction of bromoethane bromopropane would be faster.

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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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. Base
. The
imol
1. The
forme
e. Bas
perfo
In 1
Orav
cta
1. Steric hindrance is the unfavorable electron-electron repulsion that results when bonds are forced too
close to each other.
a. Draw the SN2 mechanism using curved arrows for the reaction of bromoethane with Nu:-.
siz
b. Draw the SN2 mechanism using curved arrows for the reaction of 2-bromopropane with Nu:.
vtisizvod
c. Given that steric hindrance is unfavorable, predict whether the SN2 reaction of bromoethane or 2-
bromopropane would be faster.
d. Determine in general the order of reactivity of all alkyl halides in an SN2 reaction (methyl, 1º, etc.)
Transcribed Image Text:. Base . The imol 1. The forme e. Bas perfo In 1 Orav cta 1. Steric hindrance is the unfavorable electron-electron repulsion that results when bonds are forced too close to each other. a. Draw the SN2 mechanism using curved arrows for the reaction of bromoethane with Nu:-. siz b. Draw the SN2 mechanism using curved arrows for the reaction of 2-bromopropane with Nu:. vtisizvod c. Given that steric hindrance is unfavorable, predict whether the SN2 reaction of bromoethane or 2- bromopropane would be faster. d. Determine in general the order of reactivity of all alkyl halides in an SN2 reaction (methyl, 1º, etc.)
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