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The necessary condition for a molecule t...

The necessary condition for a molecule to exhibit optical isomerism is dissymmetry or chiral. Thus all organic compounds which contain one assymetric carbon atom are chiral and exist in two stereoisomers. Although the two forms have the same structure, they have different arrangements of groups about the assymmetric carbon. In fact, they represent assymetric molecules. They do not have a plane of symmetry. They are related to each other as an object to its miror image and are non superimposable. The two structures actually stand for dextro or (+) and leavo or (-) isomers. Since they are related each other as mirror images, they are commonly called enantiomers.
Consider the following structers A,B,C,D

Which of the following statements is not correctConsider the following structers A,B,C,D

Which of the following statements is not correct

A

B and C are identical

B

A and B are enantiomers

C

A and C are enantiomers

D

B and D are enantiamers

Text Solution

Verified by Experts

The correct Answer is:
D
B and D are enantiamers
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The necessary condition for a molecule to exhibit optical isomerism is dissymmetry or chiral. Thus all organic compounds which contain one as symetric carbon atom are chiral and exist in two stereoisomers. Although the two forms have the same structure, they have different arrangements of groups about the as symmetric carbon. In fact, they represent as symetric molecules. They do not have a plane of symmetry. They are related to each other as an object to its mirror image and are non superimposable. The two structures actually stand for dextro or (+) and leavo or (-) isomers. Since they are related each other as mirror images, they are commonly called enantiomers. Consider the following structures A,B,C,D Which of the following statements is not correct

The necessary condition for a molecule to exhibit optical isomerism is dissymmetry or chiral. Thus all organic compounds which contain one assymetric carbon atom are chiral and exist in two stereoisomers. Although the two forms have the same structure, they have different arrangements of groups about the assymmetric carbon. In fact, they represent assymetric molecules. They do not have a plane of symmetry. They are related to each other as an object to its miror image and are non superimposable. The two structures actually stand for dextro or (+) and leavo or (-) isomers. Since they are related each other as mirror images, they are commonly called enantiomers. Which of the following compounds is optically inactive

The necessary condition for a molecule to exhibit optical isomerism is dissymmetry or chiral. Thus all organic compounds which contain one as symetric carbon atom are chiral and exist in two stereoisomers. Although the two forms have the same structure, they have different arrangements of groups about the as symmetric carbon. In fact, they represent as symetric molecules. They do not have a plane of symmetry. They are related to each other as an object to its mirror image and are non superimposable. The two structures actually stand for dextro or (+) and leavo or (-) isomers. Since they are related each other as mirror images, they are commonly called enantiomers. Which of the following statements is correct regarding compounds I to III

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