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The numer of optically active stereoisom...

The numer of optically active stereoisomers of tartaric acid, (HOOC.CHOH.CHOH.COOH) is

A

4

B

2

C

1

D

3

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The correct Answer is:
To determine the number of optically active stereoisomers of tartaric acid (HOOC.CHOH.CHOH.COOH), we will follow these steps: ### Step 1: Identify the Structure of Tartaric Acid Tartaric acid has the following structure: ``` HOOC | CHOH | CHOH | COOH ``` This structure contains two hydroxyl (OH) groups and two carboxylic acid (COOH) groups. ### Step 2: Identify Chiral Carbon Atoms A chiral carbon atom is defined as a carbon atom that is bonded to four different groups. In the structure of tartaric acid, we need to identify the carbon atoms: 1. The first carbon (C1) is attached to: - COOH - OH - H - CHOH (the second carbon) Since all four groups are different, C1 is a chiral carbon. 2. The second carbon (C2) is attached to: - COOH - OH - H - C1 (the first carbon) Again, all four groups are different, so C2 is also a chiral carbon. 3. The third carbon (C3) is part of the COOH group and is attached to: - OH - H - C2 (the second carbon) - Another COOH group However, C3 is not chiral because it is part of the COOH group and does not have four different groups. ### Step 3: Count the Chiral Centers From the analysis, we find that there are **two chiral carbon atoms** (C1 and C2). ### Step 4: Calculate the Number of Optically Active Stereoisomers The number of optically active stereoisomers can be calculated using the formula: \[ \text{Number of stereoisomers} = 2^n \] where \( n \) is the number of chiral centers. In this case, \( n = 2 \): \[ \text{Number of stereoisomers} = 2^2 = 4 \] ### Step 5: Determine the Number of Optically Active Isomers Since tartaric acid has two chiral centers, it can exist in multiple stereoisomeric forms. However, not all stereoisomers are optically active. Tartaric acid has a meso form, which is achiral. Therefore, the number of optically active stereoisomers is: \[ \text{Optically active stereoisomers} = 4 - 1 = 3 \] ### Conclusion The number of optically active stereoisomers of tartaric acid is **3**. ---
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RESONANCE ENGLISH-STEREOISOMERISM-EXERCISE (PART II : NATIONAL STANDARD EXAMINATION IN CHEMISTRY (NSEC) STAGE-1)
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  2. The number of all types of isomers of chlorobutane is :

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  3. (i) CH(2)=CH-CH(2)-CH=CH(2) (ii) CH(2)=CH-CH=CH-CH(3) (iii) CH(3)-...

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  4. The configurations of the carbon atoms C(2) and C(3) in the following ...

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  5. The compound that is chiral

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  6. The number of stereoisomers of compound CH(3)-CH=CH-CH(Br)CH(3) is :

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  7. The R/S designation for the following stereoisomers of 1,3-Dibromo-2-m...

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  8. Among the isomers of Dimethylcyclohexanes, the chiral ones are

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  9. Which one of the following compound has R configuration ?

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  10. The numer of optically active stereoisomers of tartaric acid, (HOOC.CH...

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  11. The above structures are related to each other as

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  12. Which of the following molecules cannot show geometric isomerism ?

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  13. 2-methylpentane is :

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  14. The two projection formulae that represent a pair of enantiomers are.

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  15. The Fischer projection formula that represents the following compounds...

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  16. Levonorgestrel is a commonly used contraceptive. The number of chiral ...

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  18. The numer of quaternary and chiral carbon atoms present in elatol, iso...

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  20. The molecule in which all atoms are not coplanar is

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