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The optically active tartaric acid is na...

The optically active tartaric acid is named as `D-(+)-` tartaric acid because it has a positive

A

Optical rotation and is derived from `D`-glucose.

B

`pH` in organic solvent.

C

Optical rotation and is derived from `D-(+)-` glyceral-dehyde.

D

Optical rotation when substituted by deuterium.

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The correct Answer is:
To solve the question regarding why the optically active tartaric acid is named `D-(+)-` tartaric acid, we can break down the reasoning step by step. ### Step-by-Step Solution: 1. **Understanding Tartaric Acid**: - Tartaric acid is a naturally occurring organic acid that has two carboxylic acid groups (-COOH) and multiple hydroxyl groups (-OH). It is a chiral molecule, meaning it has non-superimposable mirror images (enantiomers). 2. **Optical Activity**: - Optical activity refers to the ability of a compound to rotate plane-polarized light. The direction of this rotation can be either to the right (clockwise) or to the left (counterclockwise). Compounds that rotate light to the right are designated as (+) or "dextrorotatory," while those that rotate light to the left are designated as (-) or "levorotatory." 3. **D-Configuration**: - The "D" in `D-(+)-` tartaric acid refers to the configuration of the molecule based on the reference compound D-glyceraldehyde. In D-glyceraldehyde, the hydroxyl group (-OH) on the penultimate carbon (the second last carbon) is on the right side when the molecule is drawn in a Fischer projection. 4. **Positive Optical Rotation**: - The (+) sign indicates that the compound has a positive optical rotation, meaning it rotates plane-polarized light to the right. This is a characteristic of the specific stereoisomer of tartaric acid that is derived from D-glyceraldehyde. 5. **Conclusion**: - Therefore, `D-(+)-` tartaric acid is named so because it is derived from D-glyceraldehyde and exhibits positive optical rotation. ### Final Answer: The correct answer is that `D-(+)-` tartaric acid is named because it has a positive optical rotation and is derived from D-glyceraldehyde. ---

To solve the question regarding why the optically active tartaric acid is named `D-(+)-` tartaric acid, we can break down the reasoning step by step. ### Step-by-Step Solution: 1. **Understanding Tartaric Acid**: - Tartaric acid is a naturally occurring organic acid that has two carboxylic acid groups (-COOH) and multiple hydroxyl groups (-OH). It is a chiral molecule, meaning it has non-superimposable mirror images (enantiomers). 2. **Optical Activity**: ...
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CENGAGE CHEMISTRY ENGLISH-ISOMERISM-Single correct answer type (Exercise)
  1. Which of the following hydrocarbons has the lowest dipole moment?

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  2. The geometrical isomerism is shown by:

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  3. The number of geometrical isomers in CH(3)CH=N-OH is

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  4. The smallest aldehyde and its next homologue are treated with NH(2)OH ...

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  5. What are the numerical values of N and M?

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  6. Molecule in which the distance between two adjacent carbon atom is lar...

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  7. The compound which is not isomeric with diethyl ether is:

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  8. Among the following, the compound that can be most readily sulphonated...

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  9. Which of the following compounds will exhibit cis-trans (geometrical) ...

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  10. An isomer of ethanol is:

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  11. Which of the following will have the least hindered rotation about car...

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  12. The number of isomers of C(6)H(14) is:

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  13. The enolic form of acetone contains:

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  14. Three dimensional arrangements which ca be interconverted into one ano...

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  15. How many optically active stereoisomers are possible for butane-2, 3-d...

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  16. The optically active tartaric acid is named as D-(+)- tartaric acid be...

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  17. Which of the following compounds will exhibit geometrical isomerism ?

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  18. The number of isomers of the compound C(2)FClBrl is :

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  19. Which of the following compounds exhibits stereoisomerism?

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  20. In the above compound, C(2) is rotated clockwise 120^(@) about C(2)-C(...

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