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choli [55]
3 years ago
9

Draw a chair conformation for cis-1-bromo-2,4-dimethylcyclohexane showing equatorial and axial positions at the carbon atoms bea

ring the substituents (all substituents are at cis configuration) g

Chemistry
1 answer:
Ahat [919]3 years ago
6 0

Answer:

See attachment.

Explanation:

Mono-substituted cyclohexanes are more stable with their substituents in an equatorial position. However, with poly-substituted cyclohexanes, the situation is more complex since the steric effects of all substituents have to be taken into account. In this case, you can see that <u>the interconversion is shifted towards the conformation in the bottom because there is less tension between the substituents</u>.

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