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

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

`+10^(@)`

B

`-10^(@)`

C

`3^(@)`

D

`-7^(@)`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we need to calculate the observed rotation of a mixture that has undergone some degree of racemization and inversion. Here’s a step-by-step solution: ### Step 1: Understand the given data - Specific rotation of the pure enantiomer, \([α]_{pure} = +10^\circ\) - Percentage of racemization = 30% - Percentage of inversion = 70% ### Step 2: Determine the effective percentage of the enantiomer Since there is 30% racemization, this means that 30% of the original enantiomer has been converted into its opposite enantiomer. Therefore, the effective percentage of the original enantiomer remaining is: \[ \text{Effective enantiomer} = 100\% - 30\% = 70\% \] ### Step 3: Account for inversion Inversion means that the rotation due to the original enantiomer is now negative. Since 70% of the mixture is inverted, we consider this in our calculation. ### Step 4: Calculate the observed rotation Using the formula for observed rotation: \[ \text{Observed rotation} = \left( \text{Percentage of enantiomer} \times [α]_{pure} \right) / 100 \] Here, since we have 70% inversion, we will apply the negative sign: \[ \text{Observed rotation} = -\left( 70 \times 10 \right) / 100 \] \[ \text{Observed rotation} = -7^\circ \] ### Final Answer The observed rotation is \(-7^\circ\). ---
Promotional Banner

Similar Questions

Explore conceptually related problems

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 +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 ?

70% of a first order reaction was completed in 70 min . What is the half life of the reaction?

The specific rotation of two glucose anomers are alpha = + 110^(@) and beta = 19^@ and for the constant equilibrium mixtures is +52.7^@ . Calculate the percentage compositions of the anomers in the equilibrium mixture.

Pure cholesterol has a specific rotation of -32. A sample of cholesterol prepared in the lab has a specific rotation of -8. The enatiomeric excess of the sample of chloresterol is x%. X is :

A first-order reaction which is 30% complete in 30 minutes has a half-life period of

A first-order reaction which is 30% complete in 30 minutes has a half-life period of