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

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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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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 Text Predictions: On Q Search Accessibility: Investigate L SPIN D Foc D
Expert Solution
Step 1: Given compounds

2. The given compound names are shown below.

  1. Trans-1,2-cyclohexanediol;
  2. cis-1-t-butyl-2-methylcyclohexane;
  3. Trans-1-chloro-4-methylcyclohexane.

We have to draw their most stable chair conformations.


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