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Solved in 3 steps with 2 images
- A chiral center is a(n) (select all that apply): a) plane of symmetry so that there are no stereoisomers b) tetrahedral atom bonded to 4 different substituents c) tetrahedral atom d) non-superimposable mirror image e) atom bearing groups such that interchanging of any two groups leads to a stereoisomer d) enantiomerIdentify the configuration of each chiral center in the following compound I put 3,6 as chirial center, and both are R configured, but the answer was both S. The Hs are on the horizontal lines so they are coming out of the page, when low priority atom is in the front, the configuration changes. I am confused with this.Considerthe image below. a. Draw the mirror image of structure I and label it as structure II.b. Are I and II chiral?c. What kind of stereocenters do they represent?
- Identify the statements about meso compounds that are true I. II. III. IV. a. b. c. d. Meso compounds contain an internal mirror plane Meso compounds must contain at minimum two chiral centers Meso compounds may or may not be chiral Meso compounds are not superimposable on each other IandII I and III I, II, and IV I, II, III, and IVMolnupiraviris a promising drug candidate that is discovered to treat patients with Covid-19. The drug is more advantageous than Remdesivir because it is administered orally. The structure of Molnupiraviris drawn below: *Figure in the screenshot* a. How many chirality centers exist on this drug? b. How many maximum numbers of stereoisomers with respect to chiral centers exist? c. Determine R/S configuration of each chiral centeronMolnupiravirby pointing to each chiral center with an arrow on the structure above d. Draw the enantiomer of Molnupiraviracross from it above e. MolnupiravirdestroysCorona virus by introducing error during viral RNA replication. If you were a physician, would you administer a pill that consists of a racemic mixture of Molnupiravirand its enantiomer to a covid positive patient? What would be your expectations? Give your reasons.Is chiral center b r or s or neither?
- Mark all chiral center(s) with an asterisk.b. Determine the max number of possible stereoisomers that could be drawn from thisstructure. please explain each step.A chiral center is a(n) (select all possible answers) atom bearing groups such that interchanging of any two groups leads to a stereoisomer. non‑superimposable mirror image. tetrahedral atom bonded to 4 different substituents. plane of symmetry so that there are no stereoisomers. enantiomer. tetrahedral atom.Are these chiral or achiral? Is the stereo enter R(D), S(L) or neither? Please state the full name and stereocenter indicator.
- Identify the relationship between the following pairs of structures, then state whether they are enantiomers, diastereomers or identical. Help me answer iv., v., iv., vii. (last 4 sub part)Is this a chiral center? If so, R or S?Please draw this structure in wedge-dash and identify chiral centers and determine stereochem of a compound that contains a cyclohexane