Strain Energies for Monosubstituted CyclohexanesSubstituent kJ/mol Substituent kJ/mol-CN, cyano-F-I-C=CH, ethynyl 0.85-CI-Br-OH-C6H50.4Br0.5NC0.951.11.26.3-NH₂Br.-COOHCN-CH=CH₂1.95 -C(CH3)3-CH32.952.953.553.64-CH₂CH3-CH(CH3)2 4.5Click on the following structures that represent the most stable conformation of trans-1-bromo-3-cyanocyclohexane.3.6510.5BrCNBr-CN

Answered: Image /qna-images/answer/a11df6f8-36c5-49dd-b182-96e8f90dde45.jpg

Strain Energies for Monosubstituted Cyclohexanes Substituent kJ/mol Substituent kJ/mol -CN, cyano -F -I -CECH, ethynyl 0.85 -CI -Br -OH -C6H5 0.4 Br 0.5 NC 0.95 1.1 1.2 1.95 6.3 -NH₂ Br -COOH CN 7° 2.95 2.95 -CH=CH₂ -CH3 -CH₂CH3 -CH(CH3)2 4.5 -C(CH3)3 Click on the following structures that represent the most stable conformation of trans-1-bromo-3-cyanocyclohexane. 3.55 3.64 3.65 10.5 Br CN CN

Strain Energies for Monosubstituted Cyclohexanes Substituent kJ/mol Substituent kJ/mol -CN, cyano -F -I -CECH, ethynyl 0.85 -CI -Br -OH -C6H5 0.4 Br 0.5 NC 0.95 1.1 1.2 1.95 6.3 -NH₂ Br -COOH CN 7° 2.95 2.95 -CH=CH₂ -CH3 -CH₂CH3 -CH(CH3)2 4.5 -C(CH3)3 Click on the following structures that represent the most stable conformation of trans-1-bromo-3-cyanocyclohexane. 3.55 3.64 3.65 10.5 Br CN CN

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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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

Strain Energies for Monosubstituted Cyclohexanes
Substituent kJ/mol Substituent kJ/mol
-CN, cyano
-F
-I
-C=CH, ethynyl 0.85
-CI
-Br
-OH
-C6H5
0.4
Br
0.5
NC
0.95
1.1
1.2
6.3
-NH₂
Br.
-COOH
CN
-CH=CH₂
1.95 -C(CH3)3
-CH3
2.95
2.95
3.55
3.64
-CH₂CH3
-CH(CH3)2 4.5
Click on the following structures that represent the most stable conformation of trans-1-bromo-3-cyanocyclohexane.
3.65
10.5
Br
CN
Br
-CN

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