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A racemic mixtrue is optically inactive ...

A racemic mixtrue is optically inactive due to :

A

The presence of plane of symmetry

B

External compensation

C

Internal compensation

D

None of these

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To solve the question regarding why a racemic mixture is optically inactive, we can break it down into the following steps: ### Step-by-Step Solution: 1. **Understanding Racemic Mixture**: A racemic mixture consists of equal amounts of two enantiomers (optical isomers) of a chiral molecule. Enantiomers are molecules that are non-superimposable mirror images of each other. 2. **Optical Activity of Enantiomers**: Each enantiomer has the ability to rotate plane-polarized light. One enantiomer will rotate the light in a clockwise direction (dextrorotatory), while the other will rotate it in an anticlockwise direction (levorotatory). 3. **Cancellation of Optical Activity**: In a racemic mixture, since both enantiomers are present in equal amounts, the rotation caused by one enantiomer is exactly canceled out by the rotation caused by the other enantiomer. This results in no net rotation of plane-polarized light. 4. **Conclusion on Optical Inactivity**: Because the effects of the two enantiomers cancel each other out, the racemic mixture does not exhibit any optical activity. Therefore, it is considered optically inactive. 5. **Identifying the Correct Answer**: The reason for the optical inactivity of a racemic mixture is due to "external compensation," where the rotations from the two enantiomers compensate for each other. Thus, the correct answer to the question is "external compensation." ### Final Answer: A racemic mixture is optically inactive due to **external compensation**. ---

To solve the question regarding why a racemic mixture is optically inactive, we can break it down into the following steps: ### Step-by-Step Solution: 1. **Understanding Racemic Mixture**: A racemic mixture consists of equal amounts of two enantiomers (optical isomers) of a chiral molecule. Enantiomers are molecules that are non-superimposable mirror images of each other. 2. **Optical Activity of Enantiomers**: ...
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CENGAGE CHEMISTRY ENGLISH-ISOMERISM-Single correct answer type (Exercise)
  1. A compound whose molecule is superimposabel on its mirror image despit...

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  2. The IUPAC name of the compound with formula C(n)H(2n+2), having the lo...

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  3. A racemic mixtrue is optically inactive due to :

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  4. The pair of structures given below represents:

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  5. The degree of unsaturation or index of hydrogen deficiency in the foll...

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  6. The degree of unsaturation in i. C(3)H(3)Cl(3), ii. C(3)H(4)O, iii. ...

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  7. Which of the following alkenes is most stable?

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  8. Which of the following will have zero dipole moment?

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  9. The number of conformations exhibited by ethane is

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  10. Which of the following is not an isomer of butanal?

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  11. The least energetic conformation of cyclohexane is:

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  12. How many chiral carbons are present in glucose molecule CHO(CHOH)(4)CH...

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  13. The process of separation of a recemic mixture into d- and 1- componen...

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  14. If a compound has n asymmetric carbon atoms with different terminal gr...

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  15. How many chiral compounds are possible on monochlorination of 2-methyl...

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  16. A hydrocarbon with formula C(8)H(18) gives one monochloro derivative. ...

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  17. The most stained cycloalkane is :

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  18. The total number of acyclic isomers, including the stereoisomers, with...

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  19. Mesotartaric acid is optically inactive due to the presence of:

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  20. Butene when treated with chlorine at about 500^(@)C forms:

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