On a separate sheet of paper, draw the two alternative chair conformations for the product formed by the addition of bromine to 4-tert-butylcyclohexene. The Gibbs free-energy differences between equatorial and axial substituents on a cyclohexane ring are 21 kJ/mol for tert-butyl, and 2.3 kJ/mol for bromine. Calculate the ratio of the two observed products at 46.0 °C using the following equation: AG-RT ln Keq The gas constant, R, is 8.314 J/K-mol. (Enter your answer to two significant figures.) Ratio: Major to 1 Minor

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On a separate sheet of paper, draw the two alternative chair conformations for the product formed by the addition of bromine to 4-tert-butylcyclohexene. The Gibbs
free-energy differences between equatorial and axial substituents on a cyclohexane ring are 21 kJ/mol for tert-butyl, and 2.3 kJ/mol for bromine.
Calculate the ratio of the two observed products at 46.0 °C using the following equation:
AG-RT In Keq
The gas constant, R, is 8.314 J/K.mol.
(Enter your answer to two significant figures.)
Ratio:
Major
to 1
Minor
Transcribed Image Text:On a separate sheet of paper, draw the two alternative chair conformations for the product formed by the addition of bromine to 4-tert-butylcyclohexene. The Gibbs free-energy differences between equatorial and axial substituents on a cyclohexane ring are 21 kJ/mol for tert-butyl, and 2.3 kJ/mol for bromine. Calculate the ratio of the two observed products at 46.0 °C using the following equation: AG-RT In Keq The gas constant, R, is 8.314 J/K.mol. (Enter your answer to two significant figures.) Ratio: Major to 1 Minor
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