Since R isomer is 27%, it means S isomer is 63%
Now, since we see S isomer is in excess
Therefore by using the formula %(S) = (ee/2)+50
Which gives, ee= (63-50)x2 = 26%
Hence the percentage excess of the enantiomer is 26 %
what is the %ee of a mixture of enantiomer that contains 27% of the “R”enantiomer?
If a sample contains 76.0% of the R enantiomer and 24.0% of the S enantiomer, what is the enantiomeric excess of the mixture?
A mixture of enantiomers contains 84% of the R enantiomer and 16% of the Senantiomer. What is the enantiomeric excess? HTML Editor * BI А Ix 3 3 3 3 3 x?
the R-(+) enantiomer of a certain compound has a specific rotation of +52. A mixture of this compound with its enantiomer has a has an observed rotation of -26. what is the %ee of this sample and which enantiomer is in excess? what is the ration of R:S in this mixture?
9. What is the percent ee of a mixture that has 80% of one enantiomer and 20% of the other? A) 80B) 120 C) 60 D) 90
if a sample contains 83% of the R enantiomer and 17% of the S, what is the enantiomeric sxcess? the following compound is optically active or not. all 2019 Achical Be No 3 Br 03 pts.] If a sample contains 83% of the R enantiomer and 17% of the S enantiomer vhat is the enantiomeric excess of the mixture. 3 pts.1 What is the specific rotation of a sample of carvone that is an equal mixture the R and S...
Question 14 1 pts A mixture of enantiomers contains 84% of the R enantiomer and 16% of the Senantiomer. What is the enantiomeric excess?
If a mixture of (R) and (S)-Limonene Acid gives a %ee of 80.35% favoring the R 6. enantiomer, use this to calculate the ratio of R to S Limonene (review Example 3 in the procedure for how to do this) Page 2 of 2
3.34 The specific rotation of (S)-carvone (at +20°C) is +61. A chemist prepared a mixture of (R)- OF (R)- carvone and its enantiomer, and this mixture had an observed rotation of -55°. (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?
Given: Tuluene has 24% ee of (s) product, 55% yield of product, 62% of s, and 38% r. The observed rotation for the product mixture is 18.7. What is the specific rotation of the S enantiomer?
An optically active mixture has an ee value of 60% ee. What is percentage of the major enantiomerin this mixture?A. 75%B. 80%C. 60%D. 40%