2. Draw the most stable conformations of the following compounds: a) trans-1,2-cyclohexanediol b) cis-1-t-butyl-2-methylcyclohexane c) trans-1-chloro-4-methylcyclohexane
2. Draw the most stable conformations of the following compounds: a) trans-1,2-cyclohexanediol b) cis-1-t-butyl-2-methylcyclohexane c) trans-1-chloro-4-methylcyclohexane
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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Transcribed Image Text:2.
3.
Draw the most stable conformations of the following compounds:
a) trans-1,2-cyclohexanediol
b)
cis-1-t-butyl-2-methylcyclohexane
c) trans-1-chloro-4-methylcyclohexane
Using Newman projections, draw each of the following molecules in its most
stable conformation with respect to the bond indicated:
a) 2,2-dimethylpentane, C3-C4 bond;
b) 2-bromo-3-methylbutane, C2-C3 bond;
c) 2-methylbutane, C2-C3 bond;
d) 2,2-dimethylbutane, C2-C3 bond
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Step 1: Given compounds
2. The given compound names are shown below.
- Trans-1,2-cyclohexanediol;
- cis-1-t-butyl-2-methylcyclohexane;
- Trans-1-chloro-4-methylcyclohexane.
We have to draw their most stable chair conformations.
Since, you have posted multiple questions. So, we have to answer only the first question or the first three subparts according to the BartleBy Q&A guidelines. Kindly, post the remaining questions.
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