Question

If a pure R isomer has a specific rotation of –144.0°, and a sample contains 69.0%...

If a pure R isomer has a specific rotation of –144.0°, and a sample contains 69.0% of the R isomer and 31.0% of its enantiomer, what is the observed specific rotation of the mixture?

Homework Answers

Answer #1

specific rotation of R = -1440

specific rotation of S = 1440

specific rotation of mixture = specific rotation of R + specific rotation of S

                                        = -144*69/100 + 144*31/100

                                       = -99.36 +44.64 = -54.720

specific rotation of mixture = -54.720

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
If a pure R isomer has a specific rotation of –151.0°, and a sample contains 72.0%...
If a pure R isomer has a specific rotation of –151.0°, and a sample contains 72.0% of the R isomer and 28.0% of its enantiomer, what is the observed specific rotation of the mixture?
Consider a solution that contains 81.0% R isomer and 19.0% S isomer. If the observed specific...
Consider a solution that contains 81.0% R isomer and 19.0% S isomer. If the observed specific rotation of the mixture is –49.0°, what is the specific rotation of the pure R isomer?
Consider a solution that contains 74.0% R isomer and 26.0% S isomer. If the observed specific...
Consider a solution that contains 74.0% R isomer and 26.0% S isomer. If the observed specific rotation of the mixture is –73.0°, what is the specific rotation of the pure R isomer?
The specific rotation of a pure sample of the S form of compound a is +15....
The specific rotation of a pure sample of the S form of compound a is +15. A a mixture of the R and S form of "A" shows a specific rotation of +3. Provide the % enantiomeric excess and amount for each isomer in % in this mixture.
The specific rotation of (S)-carvone (at 20°C) is +61. A chemist prepared a mixture of (R)-carvone...
The specific rotation of (S)-carvone (at 20°C) is +61. A chemist prepared a mixture of (R)-carvone and its enantiomer, and this mixture had an observed rotation of -52°. (a) What is the specific rotation of (R)-carvone at 20°C? (b) Calculate the % ee of this mixture (c) What percentage of the mixture is (S)-carvone?
An optically pure sample of R-C6H5CHClCH3 with a specific rotation of -190 was converterted into the...
An optically pure sample of R-C6H5CHClCH3 with a specific rotation of -190 was converterted into the corresponding alcohol via SN1 reaction. The specific rotation of optically pure R-C6H5CHOHCH3 is -42.3 What is the specific rotation of the product? The answer is NOT -42.3 Please Explain why, because I am lost
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers....
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers. The mixture had an observed specific rotation of 16.3°. If it is known that the specific rotation of the R enantiomer is –31.9°, determine the percentage of each isomer in the mixture.
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers....
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers. The mixture had an observed specific rotation of 17.0°. If it is known that the specific rotation of the R enantiomer is –34.7°, determine the percentage of each isomer in the mixture.
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers....
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers. The mixture had an observed specific rotation of 15.8°. If it is known that the specific rotation of the R enantiomer is –33.7°, determine the percentage of each isomer in the mixture.
The specific rotation of L-alanine in water (at 25°C) is +2.8. A chemist prepared a mixture...
The specific rotation of L-alanine in water (at 25°C) is +2.8. A chemist prepared a mixture of L-alanine and its enantiomer, and 3.50 g of the mixture was dissolved in 10.0 mL of water. This solution was then placed in a sample cell with a pathlength of 10.0 cm and the observed rotation was +0.70. Calculate the % ee of the mixture.