what is the % of the S enantiomer in a sample of carvone that has a specific rotatin of -20, given that the specific rotation of R-carvone is -61?
Optical purity % = (specific rotation of sample/specific rotation of pure sample) x 100
As we have sample rotation -20, and R-carvone rotation -61, we can say that R-carvone is in excess in the sample.
optical purity % = (-20/-61) x 100 = 32.79 %
The sample has 32.79% excess of R-carvone
Remaining = 100 - 32.79 = 67.21 %
% of S-enantiomer in sample would be = 67.21/2 = 33.60 %
what is the % of the S enantiomer in a sample of carvone that has a...
vy.03- to nodollisestdinxs or snovno 10 9 63. What is the percentage of the R enantiomer in a sample of carvone that has a specific rotation of -20, given that the specific rotation of (R)-carvone is -61? A. 20% B. 66.5% C. 33.5% D. 61% Ans: Tot 1902 or bus 00-noi stor stigaganasvi novi lo l l l2 Blods 210 Slot vad v i s enworloob.10-igroviso alagi
10. What is the specific rotation of a sample of carvone that is an equal mixture of the R and S enantiomers? (R)- carvone has a specific rotation of -61°. a. -61° b. 64° d. +61° c. 0° 11. What is the percentage of the R enantiomer in a sample of carvone that has a specific rotation of 30°, given that the specific rotation of (R)-carvone is -61°? (2 pt ... this is challenging.) a. 26% b. 51% c. 49%...
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...
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?
5.54 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 -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?
If a sample of carvone gives a specific rotation of -60 and the specific rotation of (R) -carvone is -61, does the unknown sample primarily have the R or S absolute configuration?
need help with 15-17 For Problems 15-17, consider (R)-carvone (below), -61. which has a specific rotation of [a] o CH3 (t 4)S H2C CH3 15. What is the % ee of a sample of carvone that exhibits a specific rotation of -40? (1 pt) 16. What is the specific rotation of a sample of carvone that contains a 50/50 mixture of the R and S enantiomers? (1 pt) 17. If a sample of carvone gives a specific rotation of +48,...
Please help me!! 1. (8) Fill in the blank with the best word or words. What is the % of the R enantiomer in a sample of carvone that has a specific rotation of 30°, given that the specific rotation of R- carvone is -61°? What is the rate law for the following reaction? HBI How many stereoisomers have the condensed structure CHCHBICH:CHBTCH?. Write the IUPAC name for the isomer with the molecular formula CsH11Br that undergoes El elimination at...
15, 16 how do i do these? ВІ 15.03 pts.) If a sample contains 83% of the Renantiomer and and 17% of the Senantiomers what is the enantiomeric excess of the mixture. EE - 100% 16.03 pts.] What is the specific rotation of a sample of carvone that is an equal mixture of the Rand S enantiomers (R- carvone has a specific rotation of -61)?
Help please!! 1. (8) Fill in the blank with the best word or words. What is the % of the R enantiomer in a sample of carvone that has a specific rotation of 30°, given that the specific rotation of R- carvone is -610 What is the rate law for the following reaction? QH HEr How many stereoisomers have the condensed structure CH.CHBICHСHBICH?. Write the IUPAC name for the isomer with the molecular formula CsHBr that undergoes E1 elimination at...