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Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane? for UPSC 2024 is part of UPSC preparation. The Question and answers have been prepared
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Find important definitions, questions, meanings, examples, exercises and tests below for Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane?.
Solutions for Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane? in English & in Hindi are available as part of our courses for UPSC.
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Here you can find the meaning of Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane? defined & explained in the simplest way possible. Besides giving the explanation of
Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane?, a detailed solution for Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane? has been provided alongside types of Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane? theory, EduRev gives you an
ample number of questions to practice Which of the following statements most accurately describes the stereochemistry between the various cyclohexanes?A. Cis-1,2-dichlorocyclohexane and trans-1,2-dichlorocyclohexane rotate plane-polarized light in opposite directions, and together in equal proportions form a racemic mixture. B. The diaxial and diequatorial forms of trans-1,3-dichlorohexane can be separated by their differingphysical properties. C. The conformational isomers of trans-1,2-dichlorocyclohexane are enantiomers, which are not interconvertible, but resolvable.D. Only cis-1,4-dichlorocyclohexane is achiral due to a plane of symmetry, and cis-1,4- dichlorocyclohexane is diastereomeric to trans-1,4-dichlorocyclohexane? tests, examples and also practice UPSC tests.