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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trans-1-chloro-3-methylcyclohexane as well as a chair structure.
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Conformational isomers: The conformational isomers are formed by the rotation of a carbon-carbon single bond in a compound.
In the chair conformation of cyclohexane, there are two types of hydrogen atoms, axial and equatorial hydrogen atoms. By the substitution of these hydrogen atoms, we get two types of substituents in the chair conformation of cyclohexane.
The most stable chair conformation of the given compound is that which has the bulky and most substituents present at the equatorial position. In the equatorial position, there is a large space hence less steric hindrance compared to the axial position.
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