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Meso form of tartaric acid is –...

Meso form of tartaric acid is –

A

Dextorotatory

B

Laevorotatory

C

Neither Laevo nor dextro rotatory due to internal compensation

D

A mixture of equal quantities of dextro and leavo rotatory forms

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AI Generated Solution

The correct Answer is:
To determine the meso form of tartaric acid, we can follow these steps: ### Step 1: Understand the Structure of Tartaric Acid Tartaric acid is a naturally occurring organic acid with the formula C4H6O6. It has two carboxylic acid groups (-COOH) and two hydroxyl groups (-OH) attached to a carbon backbone. The structure can be represented as follows: ``` HOOC | C / \ OH C | HOOC ``` ### Step 2: Identify Chiral Centers In tartaric acid, there are two chiral centers. A chiral center is a carbon atom that has four different substituents. In the case of tartaric acid, both chiral centers are attached to different groups: 1. The first chiral carbon has -OH, -COOH, -H, and the other carbon as substituents. 2. The second chiral carbon has -OH, -COOH, -H, and the other carbon as substituents. ### Step 3: Determine the Meso Form A meso compound is a type of stereoisomer that has multiple chiral centers but is superimposable on its mirror image due to an internal plane of symmetry. For tartaric acid, if we arrange the two hydroxyl groups (-OH) on the same side (either both above or both below the plane of the molecule), we can find a plane of symmetry. This arrangement leads to the following structure: ``` HOOC | C / \ OH C | HOOC ``` In this structure, if we draw a line (the plane of symmetry) through the molecule, the upper half is a mirror image of the lower half. ### Step 4: Confirm Optical Inactivity Due to the presence of the plane of symmetry, the meso form of tartaric acid does not rotate plane-polarized light. This is because the optical activities of the two halves cancel each other out, resulting in no net rotation. This phenomenon is referred to as "internal compensation." ### Step 5: Conclusion The meso form of tartaric acid is optically inactive because of the internal compensation caused by the plane of symmetry. Therefore, the correct answer is that the meso form of tartaric acid is neither dextrorotatory nor levorotatory.
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MOTION-ISOMERISM-Exercise 1
  1. The process of separation of racemic modifications into d and l enanti...

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  2. Which of the following compounds may not exist as enantiomers?

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  3. Meso form of tartaric acid is –

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  4. How many asymmetric carbon atoms are present in - (i) 1,2-dimethyl c...

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  5. The number of geometrical isomers of CH(3)CH=CH-CH=CH-CH=CHCl is -

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  6. The number of optically active isomer possible for CH(3)-underset(OH)u...

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  7. A compound can be divided into two equal halves & contains even 'n' as...

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  8. Number of optically active isomers of tartaric acid is – underset(C...

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  9. Isomers which can be interconverted through rotation around a single b...

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  10. CH(3)-CH(2)-CH(2)-CH(3). There is free rotation about (C(2)ul(sigma)C(...

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  11. The total number of conformations of ethane is:

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  12. The eclipsed and staggered conformation of ethane is due to -

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  13. What are the type of isomers in following pairs-

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  14. At room temperature the eclipsed and the staggered forms of ethane can...

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  15. The phenomenon involving the migration of a proton to give two structu...

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  16. Which of the following compounds can exhibit tautomerism

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  17. Tautomerism is exhibited by -

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  18. Ethyl acetoacetate shows -

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  19. Which of the following does not show tautomerism ?

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  20. Which of the following shows tautomerism ?

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