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 ditferences between equatorial and axial substituents on a cyclohexane ring are 21 klimol for tert-butyl, and 23 kl/mol for bromine. Cakulate the ratio of the two observed products at 48.0 °C using the following equation: AG --RT'In Ka The gas constant, R, is 8.314 JK-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 kl/mol for tert-butyl, and 2.3 k/mol for bromine.
Calculate the ratio of the two observed products at 48.0 "C using the following equation:
AG --RT In Ka
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 kl/mol for tert-butyl, and 2.3 k/mol for bromine. Calculate the ratio of the two observed products at 48.0 "C using the following equation: AG --RT In Ka 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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