Home
Class 12
CHEMISTRY
(+) mandelic acid has a specific rot...

(+) mandelic acid has a specific rotation of `158^(@)` What would be the observed specific rotation of a mixture of 25% (-) mandelic acid and 75% (+) mandelic acid ?

A

`+118.5^(@)`

B

`-118.5^(@)`

C

`-79^(@)`

D

`+79^(@)`

Text Solution

AI Generated Solution

The correct Answer is:
To find the observed specific rotation of a mixture of mandelic acid, we can use the formula for calculating the specific rotation of a mixture of two enantiomers. The specific rotation of a mixture can be calculated using the following formula: \[ [\alpha]_{observed} = \frac{(D - L)}{(D + L)} \times [\alpha]_{pure} \] Where: - \(D\) is the percentage of the dextrorotatory enantiomer (+) mandelic acid. - \(L\) is the percentage of the levorotatory enantiomer (-) mandelic acid. - \([\alpha]_{pure}\) is the specific rotation of the pure dextrorotatory enantiomer. ### Step 1: Identify the values From the question: - \(D = 75\%\) (for (+) mandelic acid) - \(L = 25\%\) (for (-) mandelic acid) - \([\alpha]_{pure} = +158^\circ\) ### Step 2: Substitute the values into the formula Now, we can substitute the values into the formula: \[ [\alpha]_{observed} = \frac{(75 - 25)}{(75 + 25)} \times 158 \] ### Step 3: Calculate the numerator and denominator Calculate the numerator and denominator: - Numerator: \(75 - 25 = 50\) - Denominator: \(75 + 25 = 100\) ### Step 4: Simplify the fraction Now, we can simplify the fraction: \[ \frac{50}{100} = 0.5 \] ### Step 5: Calculate the observed specific rotation Now, multiply this by the specific rotation of the pure enantiomer: \[ [\alpha]_{observed} = 0.5 \times 158 = 79^\circ \] ### Conclusion The observed specific rotation of the mixture is: \[ [\alpha]_{observed} = +79^\circ \] ### Final Answer The observed specific rotation of the mixture of 25% (-) mandelic acid and 75% (+) mandelic acid is \(+79^\circ\). ---
Promotional Banner

Topper's Solved these Questions

  • ISOMERISM

    MOTION|Exercise Exercise 3|21 Videos
  • ISOMERISM

    MOTION|Exercise Exercise 4|26 Videos
  • ISOMERISM

    MOTION|Exercise Exercise 1|51 Videos
  • IONIC EQUILIBRUIM

    MOTION|Exercise Exercise -4 (Level -II)|14 Videos
  • LIQUID SOLUTION

    MOTION|Exercise EXERCISE-4 (Level-II) PREVIOUS YEAR JEE ADVANCED|19 Videos

Similar Questions

Explore conceptually related problems

Let (+) tartaric acid has a specific rotation of +11.1 , Calculate the specific rotation of a mixture of 68%(+) tartaric acid and 32%(-) tartaric acid.

The specific rotation of a pure enantiomers is +12^(@) . What will be its observed rotation if it is isolated form a reaction with 20% racemization and 80% retention.

The specific rotation of a pure enantiomers is +12^(@) . What will be its observed rotation if it is isolated form a reaction with 80% racemization and 20% inversion.

The specific rotation of a pure enantiomer is +16^@ . The observed rotation, if it is isolated from a reaction with 25% racemisation and 75% inversion is

The specific rotation of a pure enantiomer is +16^(@) its observed rotation if it is isolated from a reaction with 25% racemisation and 75% retention is,

(R)-2-methyl-1-butanol has a specific rotation of +13.5^(@) . The specific rotation of 2-methyl-1-butanol containing 40% of the (S)-enantiomer is _____

The specific rotation of a pure enantiomer is +10^(@) . The observed rotation, if it is isolated from a reaction with 30% recemisation and 70% inversion is

a. The specific rotation of a pure enantiomer is +10^(@) . What will be its observed rotation if its is isolated from a reaction with i. 30% racemisation and 70% retention. ii. 70% racemisation and 30% inversion. b. What is the percentage composition of a mixtrue of two enantiomers whose rotation is -10^(@) ? The specific rotation of pure enantiomers is -20^(@) . c. What is the optical purity of a sample having an [alpha]_(obs.)=+9.0^(@) if [alpha]_(D)=+12^(@) .

MOTION-ISOMERISM-Exercise 2
  1. When 20 gm optically active compound is placed in a 10 dm tube, in a 2...

    Text Solution

    |

  2. Dextrorotary alpha- pinene has a specific rotation [alpha](D)^(2...

    Text Solution

    |

  3. (+) mandelic acid has a specific rotation of 158^(@) What wou...

    Text Solution

    |

  4. How many stereoisomers of (CH(3) )(2) CHCH= CHCH(2) CH(OH) CH(2) ...

    Text Solution

    |

  5. How many stereoisomers of the following molecule are possible? HOOC-...

    Text Solution

    |

  6. Which of the following statements must be true for two pure chiral iso...

    Text Solution

    |

  7. Which of the following statement is correct ?

    Text Solution

    |

  8. The prefered conformation of trans-1, 2- dibromocyclohexane is:

    Text Solution

    |

  9. Which of the following sugars has the configuration (2S 3R, 4R) ?

    Text Solution

    |

  10. Number of geometrical isomer of given compound will be :

    Text Solution

    |

  11. The total number of optically active alkynes having molecular formula ...

    Text Solution

    |

  12. How many stereoisomer are possible for the following molecule ?

    Text Solution

    |

  13. How many stereoisomers are possible for the following compound ?

    Text Solution

    |

  14. How many stereoisomer may have this natural occuring compound.

    Text Solution

    |

  15. Molecular formular C(3) H(6) Br(2) can have (including stereoisomers):

    Text Solution

    |

  16. The number of isomers of c(3) H(5) Br(3) (including stereoisomers )

    Text Solution

    |

  17. The number of optically active compounds in the isomers of C(4) H(9)Br...

    Text Solution

    |

  18. Number of possible isomers of glucose is :

    Text Solution

    |

  19. How many total isomers are possible by replacing one hydrogens atoms o...

    Text Solution

    |

  20. On chlorination of propane number of products of the formula C(3)H(6)...

    Text Solution

    |