For cis-4-t-butylcyclohexanol and tras-4-t-butylcyclohexanol, why do the two isomeric products have different relative chromatographic movements?
For cis-4-t-butylcyclohexanol and tras-4-t-butylcyclohexanol, why do the two isomeric products have different relative chromatographic movements?
Homework Answers
Yes. two isomeric products, cis and trans -4-t-butylcyclohexanol will have different chromatographic moveents. Depends upon the interaction of hydroxyl group interaction with the chromatographic plate, it will move. In trans product, OH group is freely appear so it will interact with chromatographic plate more so it has high polarity. In cis,isomer there is a steric hindrance so, we can expect it will move faster.
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For cis-4-t-butylcyclohexanol and tras-4-t-butylcyclohexanol,
why do the two isomeric products have different relative
chromatographic movements?
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