Identify the major and minor product(s) of the following reaction: A. OH conc. H,50 Heat Major product(s): OH ? B. Identify the major and minor product(s) of the following reaction: C. Identify the major and minor product(s) of the following reaction: NaOEt NICH ? ? Major product(s): रा eTextbook and Media eTextbook and Media Minor product(s): Minor product(s): @ Oth OH Major product(s): EtO (racemic) eTextbook and Media Minor product(s): D. There are two stereoisomers of 1-tert-butyl-4-chloro-cyclohexane. One of these isomers reacts with sodium ethoxide in an E2 reaction that is 500 times faster than the reaction of the other isomer. Identify the isomer that reacts faster, and explain the difference in rate for these two isomers. fizi The an isomer rapidly undergoes an E2 reaction because it is locked in a chair conformation in which the chlorine occupies position, as shown in drawing antiperiplanar to a beta proton. Because of the bulky tert-butyl group, the and the leaving group -isomer is essentially locked in a chair conformation in which the chlorine occupies an position, as shown in drawing and the leaving group is not antiperiplanar to a beta proton. EtO (racemic)

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Chapter1: Chemical Foundations
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Identify the major and minor product(s) of the following reaction:
A.
OH
conc. H,50
Heat
Major product(s):
OH
?
B.
Identify the major and minor product(s) of the following reaction:
C.
Identify the major and minor product(s) of the following reaction:
NaOEt
NICH
?
?
Major product(s):
रा
eTextbook and Media
eTextbook and Media
Minor product(s):
Minor product(s):
@ Oth
OH
Major product(s):
EtO
(racemic)
eTextbook and Media
Minor product(s):
D.
There are two stereoisomers of 1-tert-butyl-4-chloro-cyclohexane. One of these isomers reacts with sodium ethoxide in an E2
reaction that is 500 times faster than the reaction of the other isomer. Identify the isomer that reacts faster, and explain the difference
in rate for these two isomers.
fizi
The
an
isomer rapidly undergoes an E2 reaction because it is locked in a chair conformation in which the chlorine occupies
position, as shown in drawing
antiperiplanar to a beta proton.
Because of the bulky tert-butyl group, the
and the leaving group
-isomer is essentially locked in a chair conformation in which the chlorine
occupies an
position, as shown in drawing
and the leaving group is not antiperiplanar to a beta proton.
EtO
(racemic)
Transcribed Image Text:Identify the major and minor product(s) of the following reaction: A. OH conc. H,50 Heat Major product(s): OH ? B. Identify the major and minor product(s) of the following reaction: C. Identify the major and minor product(s) of the following reaction: NaOEt NICH ? ? Major product(s): रा eTextbook and Media eTextbook and Media Minor product(s): Minor product(s): @ Oth OH Major product(s): EtO (racemic) eTextbook and Media Minor product(s): D. There are two stereoisomers of 1-tert-butyl-4-chloro-cyclohexane. One of these isomers reacts with sodium ethoxide in an E2 reaction that is 500 times faster than the reaction of the other isomer. Identify the isomer that reacts faster, and explain the difference in rate for these two isomers. fizi The an isomer rapidly undergoes an E2 reaction because it is locked in a chair conformation in which the chlorine occupies position, as shown in drawing antiperiplanar to a beta proton. Because of the bulky tert-butyl group, the and the leaving group -isomer is essentially locked in a chair conformation in which the chlorine occupies an position, as shown in drawing and the leaving group is not antiperiplanar to a beta proton. EtO (racemic)
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