The following compounds are stereoisomers. Rank in order of increasing the stability (the least stable to the most stable.) CI OH A. SUBSTITUENT -CI -OH -CH3 -CH₂CH3 -CH(CH3)2 -C(CH3)3 A
The following compounds are stereoisomers. Rank in order of increasing the stability (the least stable to the most stable.) CI OH A. SUBSTITUENT -CI -OH -CH3 -CH₂CH3 -CH(CH3)2 -C(CH3)3 A
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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both
![The following compounds are stereoisomers. Rank in order of increasing the stability (the least stable to the most stable.).
CI OH
A.
SUBSTITUENT
-CI
-OH
-CH3
-CH₂CH3
-CH(CH3)2
-C(CH3)3
A<C< B <D
D<B<A <C
C<A<B<D
A<B<C<D
OD<C<B<A
CI
B.
OH
CI
1,3-DIAXIAL INTERACTIONS
(KJ/MOL)
2.0
4.2
7.6
8.0
9.2
22.8
C.
CI
D.
EQUATORIAL-AXIAL RATIO
(AT EQUILIBRIUM)
70: 30
83 17
95:5
96:4
97:3
9999 : 1
OH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F19a6b6af-96fa-49d6-a477-e3a40b254e0f%2F90d0bfc5-8346-4416-8f6a-9722f82f7fec%2Fwjrs5k_processed.png&w=3840&q=75)
Transcribed Image Text:The following compounds are stereoisomers. Rank in order of increasing the stability (the least stable to the most stable.).
CI OH
A.
SUBSTITUENT
-CI
-OH
-CH3
-CH₂CH3
-CH(CH3)2
-C(CH3)3
A<C< B <D
D<B<A <C
C<A<B<D
A<B<C<D
OD<C<B<A
CI
B.
OH
CI
1,3-DIAXIAL INTERACTIONS
(KJ/MOL)
2.0
4.2
7.6
8.0
9.2
22.8
C.
CI
D.
EQUATORIAL-AXIAL RATIO
(AT EQUILIBRIUM)
70: 30
83 17
95:5
96:4
97:3
9999 : 1
OH
![In the following five isomers, which compounds can have the most stable conformer? (each isomer has two chair conformations.)
B
C
D
Et
Et
Me
La 1818-18.
t-Bu
Me
'Me t-Bu
A
t-Bu
SUBSTITUENT
-CI
-OH
-CH3
-CH₂CH3
-CH(CH3)2
-C(CH3)3
A
Et
B
E
Me
1,3-DIAXIAL INTERACTIONS
(KJ/MOL)
2.0
4.2
7.6
8.0
9.2
22.8
t-Bu
Et
EQUATORIAL-AXIAL RATIO
(AT EQUILIBRIUM)
70: 30
83: 17
95:5
96:4
97:3
9999: 1
E
t-Bu
'Me](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F19a6b6af-96fa-49d6-a477-e3a40b254e0f%2F90d0bfc5-8346-4416-8f6a-9722f82f7fec%2Fsiepdpn_processed.png&w=3840&q=75)
Transcribed Image Text:In the following five isomers, which compounds can have the most stable conformer? (each isomer has two chair conformations.)
B
C
D
Et
Et
Me
La 1818-18.
t-Bu
Me
'Me t-Bu
A
t-Bu
SUBSTITUENT
-CI
-OH
-CH3
-CH₂CH3
-CH(CH3)2
-C(CH3)3
A
Et
B
E
Me
1,3-DIAXIAL INTERACTIONS
(KJ/MOL)
2.0
4.2
7.6
8.0
9.2
22.8
t-Bu
Et
EQUATORIAL-AXIAL RATIO
(AT EQUILIBRIUM)
70: 30
83: 17
95:5
96:4
97:3
9999: 1
E
t-Bu
'Me
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