3. Mechanism: Show a detailed reaction mechanism for the following reaction. Include the structure of the expected products and appropriate stereochemistry for all steps. Assume all reagents are in excess. CI-CI H-Oom hin H step 1 sifzodie lyne step 2 4 step 3 wellot smys 4 bers product(s) a. The name of this mechanism is: b. This reaction follows inversion / scrambling / syn / anti/ other stereoselectivity. c. This reaction follows Hofmann / Saytzev / Markovnikov / anti-Markovnikov / none / other regioselectivity.

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter16: Aldehydes And Ketones
Section: Chapter Questions
Problem 16.63P
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Mechanism: Show a detailed reaction mechanism for the following reaction. Include the structure of the expected products and appropriate stereochemistry for all steps. Assume all reagents are in excess.

3. Mechanism:
Show a detailed reaction mechanism for the following
reaction. Include the structure of the expected products and appropriate
stereochemistry for all steps. Assume all reagents are in excess.
Asunt ad
H-O
H
CI-CI
step 1
oil zodi
051912
gontoplo siv ons lla
dira epl on sell of H
step 2
4
foib lanimey
step 3
avollot
nab terli
odlazovie onvolle na to
product(s)
s as of bobbe
a.
The name of this mechanism is:
b. This reaction follows inversion / scrambling / syn / anti/ other stereoselectivity.
This reaction follows Hofmann / Saytzev/ Markovnikov / anti-Markovnikov /
none / other regioselectivity.
c.
The purpose of CH3OH in this reaction is
d.
and
none. We do / do not expect carbocation rearrangements in this mechanism.
f. If we switched the solvent to CCl4 we would get the same / a different
mechanism and the same / a different product.
Transcribed Image Text:3. Mechanism: Show a detailed reaction mechanism for the following reaction. Include the structure of the expected products and appropriate stereochemistry for all steps. Assume all reagents are in excess. Asunt ad H-O H CI-CI step 1 oil zodi 051912 gontoplo siv ons lla dira epl on sell of H step 2 4 foib lanimey step 3 avollot nab terli odlazovie onvolle na to product(s) s as of bobbe a. The name of this mechanism is: b. This reaction follows inversion / scrambling / syn / anti/ other stereoselectivity. This reaction follows Hofmann / Saytzev/ Markovnikov / anti-Markovnikov / none / other regioselectivity. c. The purpose of CH3OH in this reaction is d. and none. We do / do not expect carbocation rearrangements in this mechanism. f. If we switched the solvent to CCl4 we would get the same / a different mechanism and the same / a different product.
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