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if a sample contains 83% of the R enantiomer and 17% of the S, what is...
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)?
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?
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?
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,...
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%...
An attempt at synthesizing a certain optically active compound resulted in a mixture of its enantiomers. The mixture had an observed specific rotation of +11.7. If it is known that the specific rotation of the R enantiomer is -38.9, determine the percentage of each isomer in the mixture. Number R enantiomer: % Number S enantiomer
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?
Question 14 1 pts A mixture of enantiomers contains 84% of the R enantiomer and 16% of the Senantiomer. What is the enantiomeric excess?
11. Determine the absolute configuration of each asymmetric center in the following molecule CH2CH2CH2CH3 12. What is the enantiomeric composition of a mixture that has a specific rotation of +88 degrees and has an enantiomeric excess of 40%. What are specific rotations of each enantiomer? 13. Determine if each of the following pairs of compounds represent enantiomers, diastereomers, constitutional isomers, or two molecules of the same compound CH H+CH н-н H -Br BH CHE