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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 differing
physical 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?
Most Upvoted Answer
Which of the following statements most accurately describes the stereo...
- **Cis-1,4-dichlorocyclohexane and trans-1,4-dichlorocyclohexane stereochemistry**
**Explanation:**
- Cis-1,4-dichlorocyclohexane is achiral due to having a plane of symmetry, which allows for superimposition of the molecule on its mirror image.
- Trans-1,4-dichlorocyclohexane is diastereomeric to cis-1,4-dichlorocyclohexane because they are not mirror images of each other and have different physical properties.
- The presence of a plane of symmetry in cis-1,4-dichlorocyclohexane makes it optically inactive, while trans-1,4-dichlorocyclohexane lacks a plane of symmetry and can exhibit optical activity.
- Therefore, the stereochemistry of cis-1,4-dichlorocyclohexane and trans-1,4-dichlorocyclohexane differs due to the presence or absence of a plane of symmetry and their ability to rotate plane-polarized light.
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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?
Question Description
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 according to the UPSC exam syllabus. Information about 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? covers all topics & solutions for UPSC 2024 Exam. 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. Download more important topics, notes, lectures and mock test series for UPSC Exam by signing up for free.
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.
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