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draw the scructure of Masoprocol and
Circle five chiral carbons of Masoprocol
Step by step
Solved in 2 steps with 1 images
- If a chiral carbon has the following substituents: -OH, -NH2, -COOH, and -OCH3 arrange them in order of prioritization (highest priority to lowest priority)? a -OCH3 > -OH > -NH2 > -COOH b -OCH3 > -NH2 > - OH > -COOH c -OH > - OCH3 > -NH2 > -COOH d -COOH > -NH2 > -OH > -OCH3Explain why HC = CH is more acidic than CH3CH3, even though the C - H bond in HC = CH has a higher bond dissociation energy than the C - H bond in CH3CH3Assign the absolute configuration to each chiral centers (signed with *).
- Determine absolute configurations for the double bond and chiral carbon for the molecule shown. OH double chiral bond carbon m A) E B) E C) Z D) Z MRSASA) ОН B) HO. Molecule A is achiral and molecule B is chiral Molecule A is chiral and molecule B is achiral Both molecules are achiral. Both molecules are chiral.2. Assign priorities to the groups on this chiral carbon. Label it as R or S. QH HÖ ÓCH3
- Ephedrine, a stimulant and illegal drug is an optically active compound with two chiral centers. OH NHCH3 CH3 Ephedrine a. In the structure of ephedrine on the answer sheet, mark each chiral center with an asterisk. b. How many stereoisomer/s does ephedrine have? Show necessary solutions on the answer sheet. c. Compound EPS is a stereoisomer of ephedrine. Determine the absolute configuration (R or S) at carbons A and B of compound EPS.8. Assign each chiral carbon as R or S in compound-A. Draw the mirror image of compound-A and assign configuration to each chiral carbon. (note that the dotted line represents the mirror). H₂N S OH Compound A CH3 CH3 mirror CH3 CH 3 Mmok NHZWhat are the points need to keep in mind, When trying to distinguish between chiral and achiral compounds ?