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An organic compound P exists in two enan...

An organic compound P exists in two enantiomeric forms, which have specific optical rotation values `[alpha] = +-100^(@)`. The optical rotation of a mixture of these two enantiomers is `-50^(@)`. Calculate the percentage of that enantiomer which is in lower concentration in the mixture.

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To solve the problem, we need to determine the percentage of the enantiomer that is present in lower concentration in a mixture of two enantiomers of compound P. The specific optical rotations of the enantiomers are given as +100° and -100°, and the observed optical rotation of the mixture is -50°. ### Step-by-Step Solution: 1. **Understanding the Optical Rotation Values**: - The specific rotation of the dextrorotatory enantiomer (let's call it D) is +100°. - The specific rotation of the levorotatory enantiomer (let's call it L) is -100°. - The observed rotation of the mixture is -50°. 2. **Using the Enantiomeric Excess Formula**: - The enantiomeric excess (EE) can be calculated using the formula: \[ EE = \frac{\text{Observed Rotation}}{\text{Specific Rotation of Pure Enantiomer}} \times 100 \] - Since the observed rotation is -50° and we will use the absolute value of the specific rotation of the pure enantiomer (which is 100°), we can substitute: \[ EE = \frac{-50}{100} \times 100 = -50\% \] 3. **Calculating the Concentrations**: - The enantiomeric excess indicates that the mixture is not racemic. The total percentage of the two enantiomers must add up to 100%. - Let \( x \) be the percentage of the dextrorotatory isomer (D), and \( y \) be the percentage of the levorotatory isomer (L). - We know: \[ x + y = 100\% \] - The enantiomeric excess can also be expressed as: \[ EE = \frac{x - y}{x + y} \times 100 \] - Substituting \( x + y = 100\% \): \[ EE = \frac{x - (100 - x)}{100} \times 100 = \frac{2x - 100}{100} \times 100 = 2x - 100 \] - Setting this equal to -50%: \[ 2x - 100 = -50 \] - Solving for \( x \): \[ 2x = 50 \implies x = 25\% \] 4. **Finding the Percentage of the Lower Concentration Enantiomer**: - Since \( x \) (the percentage of D) is 25%, the percentage of L (the levorotatory isomer) is: \[ y = 100 - x = 100 - 25 = 75\% \] - Therefore, the percentage of the enantiomer in lower concentration (D) is **25%**. ### Final Answer: The percentage of the enantiomer which is in lower concentration in the mixture is **25%**.

To solve the problem, we need to determine the percentage of the enantiomer that is present in lower concentration in a mixture of two enantiomers of compound P. The specific optical rotations of the enantiomers are given as +100° and -100°, and the observed optical rotation of the mixture is -50°. ### Step-by-Step Solution: 1. **Understanding the Optical Rotation Values**: - The specific rotation of the dextrorotatory enantiomer (let's call it D) is +100°. - The specific rotation of the levorotatory enantiomer (let's call it L) is -100°. - The observed rotation of the mixture is -50°. ...
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RESONANCE ENGLISH-STEREOISOMERISM-EXERCISE (PART III : PRACTICE TEST-2 (IIT-JEE (ADVANCED PATTERN))
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  2. In the given energy graph for cyclohexane, the point "B" represent.

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  3. Identify the most stable stereoisomer :

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  9. Which of the following compounds can show Optical isomerism as well as...

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  10. Which of the following compound will show geometrical isomerism?

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  11. Which of the following statement(s) is/are true about the following co...

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  12. An organic compound P exists in two enantiomeric forms, which have spe...

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  13. Total number of meso forms possible for 1,2,3,4 -Tetrachlorocyclobutan...

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  14. If "A" is total number of meso compounds and "B" is total number of op...

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  15. Sum of total no. of stereoisomers (A) and total no. of fractions (B) f...

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  16. Which of the following carbonyl compound will give two products after ...

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  17. Total number of stereoisomers of truxillic acid are :

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