2. what is the ratio of enantiomers in a mixture with an enantiomeric excess of 50%?
Given that the enantiomeric excess of the mixture is 50% i.e one of the isomer is present in 50% excess when compared to the isomer. Remaining 50% of the mixture contains 25% one enantiomer and 25% of the opposite enantiomer.
Now, finally in the reaction mixture contains 75% of the enantiomer and 25% of the opposite enantiomer.
The ratio of the enantiomers in a mixture with an enantiomeric excess of 50% is 75: 25 = 3:1
2. what is the ratio of enantiomers in a mixture with an enantiomeric excess of 50%?...
3. a) Draw the structure of (2S,3S)-2,3-difluorobutane in an extended zig-zag line drawing using wedged and dashed bonds where appropriate. b) Is (2S,3S)-2,3-difluorobutane optically active? Explain
If the enantiomeric excess of a mixture is 77%, what are the % compositions of the major and minor enantiomers?
the enantiomeric excess for the following mixture of enantiomers A and B (5.12D)? 11. (1 point) What is enantio 85% A and 1500 B (2 points) Name the following molecules including absolute configuration (R or S) of each asymmetric carbon: Assign priorities a, b, c, & d. 8. a) d Ci oi 25, 3R -3,3-diuhloro pentau Cl b)
3. Indicate the relationship as enantiomers, diasteriomers or identical compounds in the space belom Two meso compounds should be identified as identical 2 pts. Each 6 pts. Total Note: Same substituents are on each chiral center 4. D-Flemsoaric acid has a specific rotation of +67". What is the enantiomeric excess and which isomer DorL will be in excess. If a mixture of D and L Flemsoaric acid has a specific rotation of -42°. Enantiomeric Excess = Name of isomer in...
6. Draw the two chair conformations for cis-1-sec-butyl-2-ethylcyclohexane. Predict the most stable conformer and draw the corresponding Newman projection (4 pts) 7. Convert the following compounds from their 3D structure to their Fisher projection and vice-versa (4 pts) НО Br HO co₂me HN CI CO2Me НО -СІ НЕОН СН2ОН 5| Page 8. The specific rotation for (R)-methyl 2-chloro-2,3-dihydroxypropanoate is -126.7. A student prepare a sample of methyl 2-chloro-2,3-dihydroxypropanoate enantiomers that shows a specific rotation of +89.6, (a) Calculate the percent...
What is the enantiomeric excess of a compound that shows a specific rotation (aj +18.6, where the pure enantiomer has a reference value of a 24.87 a 75 b0%, racemic mixture 0 2660 o ason 21.5
2. The optical activity, measured by specific rotation, of pure (R-malic acid is [a]20D-+27% What is the specific rotation of a mixture of 50% and 50% of (R)-malic acid and (S)-malic acid? What is enantiomeric excess of a sample of malic acid containing both enantiomers that has a [al20D -0% [a]20D-27"; [a]20D-_ 13.5": [a]20D-+ 13.5°
QUESTION 11 11. What is the enantiomeric excess of a mixture containing 6.0 g of (-)-glyceraldehyde and 2.0 of (+)-glyceraldehyde? A) 25% B) 50% C) 60% D) 75% . on > QUESTION 12 Al identical
3. For the structure below determine the number of stereocenters. Determine the number of stereoisomers for the structure and draw all of them? Determine the enantiomers and which are diasteriomers. Determine the absolute configuration for both for both enantiomers. 10 pts 4. What would be the observed optical rotation of a sample of 3.2 R of pure (.) - 3-chloropentanoic acid with a specific rotation of 30.0 degrees in 100 ml of water, measured in 25 cm cuvette. 4 pts...
2) Natural epinephrine (with a specific rotation of -50°) is used medicinally. Its enantiomer is medically worthless and is, in fact, toxic. You, a pharmacist, are given a solution said to contain epinephrine, but the optical purity is not mentioned. You place it in a polarimeter and get an observed optical rotation of -150. What is the enantiomeric excess of natural epinephrine? How much of each enantiomer is in the mixture? You must show your work to get credit.