Home
Class 12
CHEMISTRY
The specific rotation of a pure enantiom...

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

A

`+12^@`

B

`-12^@`

C

`4^@`

D

`-4^@`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we need to calculate the observed rotation of a compound that has undergone racemization and inversion. Here’s a step-by-step breakdown of the solution: ### Step 1: Understand the Given Information - The specific rotation of the pure enantiomer (\[ \alpha_{pure} \]) is \( +16^\circ \). - There is 25% racemization and 75% inversion. ### Step 2: Determine the Effect of Inversion Inversion means that the configuration of the compound is changed, but the specific rotation remains the same. Since 75% of the original enantiomer undergoes inversion, we can calculate the contribution from this part. ### Step 3: Calculate the Contribution from Inversion The contribution from the 75% that remains as the original enantiomer can be calculated as follows: \[ \text{New specific rotation due to inversion} = \text{Specific rotation} \times \text{Retention} \] \[ \text{New specific rotation due to inversion} = +16^\circ \times 0.75 = +12^\circ \] ### Step 4: Determine the Effect of Racemization Racemization means that 25% of the original enantiomer converts into its enantiomer. Therefore, the rotation due to racemization will be the average of the specific rotations of both enantiomers, which is 0 because they are equal in magnitude but opposite in sign. ### Step 5: Calculate the Observed Rotation The observed rotation (\[ \alpha_{observed} \]) can be calculated by considering the contributions from both the inverted and racemized components: - 75% of the original enantiomer contributes \( +12^\circ \). - 25% of the original enantiomer contributes \( 0^\circ \) (due to racemization). Thus, the observed rotation is simply: \[ \alpha_{observed} = +12^\circ + 0^\circ = +12^\circ \] ### Final Answer The observed rotation, if it is isolated from a reaction with 25% racemization and 75% inversion, is \( +12^\circ \). ---
Promotional Banner

Similar Questions

Explore conceptually related problems

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

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.

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.

Cholesterol, when isolated from natural sources, is obtained as a single enantiomer. The observed rotation alpha of a 0.3 g sample of cholesterol in 5mL of chloroform solution contained in a 10 cm polarimeter tube is -0.78^(@) . Calculate the specific rotation of cholesterol. A sample of synthetic cholesterol was prepared consisting entirely of (+)-cholesterol. This synthetic (+)-cholesterol was mixed with some natural (-)-cholesterol. The mixture had a specific rotation [alpha]_(D)^(20) " of " -13^(@). What fraction of the mixture was (+)-cholesterol ?

D (+) Glucose has melting point 146^@ C and specific rotation [alpha]_(D)^(25) is + 112^@ C. Another D(+) Glucose has melting point 150^@ C and specific rotational [alpha]_(D)^(25) is + 18.7^@ C. The two form have significantly different optical rotation but when an aqueous solution of either form is allowed to stand, it rotation changes. The specific rotation of one form decreases and rotation of other increases until both solution show the same value +52.7^@ . The change in rotation towards an equilibrium value is called mutarotation. Mutarotation is characteristic feature of:

D (+) Glucose has melting point 146^@ C and specific rotation [alpha]_(D)^(25) is + 112^@ C. Another D(+) Glucose has melting point 150^@ C and specific rotational [alpha]_(D)^(25) is + 18.7^@ C. The two form have significantly different optical rotation but when an aqueous solution of either form is allowed to stand, it rotation changes. The specific rotation of one form decreases and rotation of other increases until both solution show the same value +52.7^@ . The change in rotation towards an equilibrium value is called mutarotation. For mannose the mutarotation can be shown in brief as follow:

A reaction is 50% complete in 2 hours and 75% complete in 4 hours. What is the order of the reaction ?