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(A): Meso tartaric acid is optically ina...

(A): Meso tartaric acid is optically inactive
(R): Meso tartaric acid has no asymmetric carbon

A

Both (A) and (R) are true and (R) is the correct explanation of (A)

B

Both (A) and (R) are true and (R) is not the correct explanation of (A)

C

(A) is true but (R) is false

D

(A) is false but (R) is true

Text Solution

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The correct Answer is:
C

(A) is true but (R) is false
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AAKASH SERIES-ISOMERISM -PRACTICE SHEET (EXERCISE-III) STRAIGHT OBJECTIVE TYPE QUESTIONS)
  1. In the representation of specific rotation ([alpha](D)^(250C)), .D. in...

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  2. A molecule as a whole is asymmetric if it does not possess

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  3. For an optically active compound specific rotation ([alpha](D)^(25)) d...

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  4. Which of the following exists in enantiomeric pair

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  5. When two or more isotopic atoms are connected to the asymmetric chiral...

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  6. (A): Meso tartaric acid is optically inactive (R): Meso tartaric aci...

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  7. (+-) Lactic acid is optically inactive due to

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  8. If the specific rotation produced by the compound ‘A’is +52^(@), the...

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  9. The incorrect statement about

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  10. The pair of structures given below represent

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  11. Which of the following statements is not correct regarding enantiomers...

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  12. Which of the following can show optical isomerism

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  13. 2, 3-pentadiene is optically active since it

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  14. How many chiral carbon atoms are present in 2, 3, 4 -trichoropentane?

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  15. How many isomers could be obtained by replacing one hydrogen of propen...

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  16. For an optically active compound alpha(obs) depends on

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  17. Which statement is incorrect about diastereomers

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  18. If a compound has ‘n’ different types of asymmetric carbon atoms then ...

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  19. For tartaric acid total number of possible stereo isomers (configurati...

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  20. Total number of possible isomers (configuartional only ) for 2,3,4- tr...

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