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The most stable conformation of the compound shown has: CH CH CH O all methyl groups are equatorial O None of these O equatorial methyl groups at C-1 and C-3; axial at C-2 equatorial methyl groups at C-2 and C-3; axial at C-1 O equatorial methyl groups at C-1 and C-2; axial at C-3

The most stable conformation of the compound shown has: CH CH CH O all methyl groups are equatorial O None of these O equatorial methyl groups at C-1 and C-3; axial at C-2 equatorial methyl groups at C-2 and C-3; axial at C-1 O equatorial methyl groups at C-1 and C-2; axial at C-3

Chemistry
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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The image displays a cyclohexane ring with methyl groups attached at the 1, 2, and 3 positions. The accompanying question asks: "The most stable conformation of the compound shown has:" Options: - O all methyl groups are equatorial - O None of these - O equatorial methyl groups at C-1 and C-3; axial at C-2 - O equatorial methyl groups at C-2 and C-3; axial at C-1 - O equatorial methyl groups at C-1 and C-2; axial at C-3 The diagram shows a skeletal structure of a cyclohexane molecule, with each carbon atom of the ring labeled from 1 to 3. Methyl groups (CH₃) are attached at these positions. The question involves analyzing the stability based on the positions (axial vs. equatorial) of these methyl groups.
Transcribed Image Text:The image displays a cyclohexane ring with methyl groups attached at the 1, 2, and 3 positions. The accompanying question asks: "The most stable conformation of the compound shown has:" Options: - O all methyl groups are equatorial - O None of these - O equatorial methyl groups at C-1 and C-3; axial at C-2 - O equatorial methyl groups at C-2 and C-3; axial at C-1 - O equatorial methyl groups at C-1 and C-2; axial at C-3 The diagram shows a skeletal structure of a cyclohexane molecule, with each carbon atom of the ring labeled from 1 to 3. Methyl groups (CH₃) are attached at these positions. The question involves analyzing the stability based on the positions (axial vs. equatorial) of these methyl groups.
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