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 32.0 °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: to 1 Major 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 32.0 °C using the following equation:
AG° = -RT In Keg
The gas constant, R, is 8.314 J/K mol.
(Enter your answer to two significant figures.)
Ratio:
to 1
Major
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 32.0 °C using the following equation: AG° = -RT In Keg The gas constant, R, is 8.314 J/K mol. (Enter your answer to two significant figures.) Ratio: to 1 Major Minor
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