Indicate which atoms in the following compound are chiral centers. NH2 HO HO a CH3 (Provide a list of letters without spacing. Alphabetize your list (abcd).) Chiral centers: How many stereoisomers do you expect for this compound?
Q: Indicate which atoms in the following compound are chiral centers. H3C. HO H3C CH2 (Provide a list…
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Q: 1. Determine the number of chiral centers in each molecule below. Label each with an asterisk. HO b.…
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A: Following are the chiral centres and appropriate R/S notation.
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Q: please find attachment.
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A: For configuration of chiral center we use cahn-ingold-prelog rule .
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Q: How many chirality center/s are in this molecule? OH H3C-CH,CHCH2CH3
A: Number of chiral centre in the molecules -
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- 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)Specify the configurations (R or S) at ALL chiral centers in the molecules below. Please note that some molecules below may have more than 1 chiral centers, and you are responsible to find all the chiral centers.Hi, I need help with 7c. For 7a I got 3 asymmetric centers and for 7b I got 8 possible stereoisomers.
- Identify the configuration of each chiral center of the following compounds: In the boxes below, first, input the number(s) corresponding to the chiral center(s) in numerical order as a comma separated list with no spaces (e.g "1,3,4"). Then input the configuration(s) of the chiral center(s) in the same order and format (e.g.." R,S,S"). Chiral center location(s): Configuration(s):Molnupiraviris 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.Build 2‑bromoethan‑1‑ol and its mirror image. 2‑Bromoethan‑1‑ol, which has condensed structural formula BrCH2CH2OH, is also called 2‑bromoethanol. a. Draw the structures of 2‑bromoethan‑1‑ol and its mirror image using wedges and dashed wedges. b. How many stereocentres are present in 2‑bromoethan‑1‑ol? c. Are the molecules chiral? Do they contain planes of symmetry? Briefly explain the evidence for your answer.
- Using flying wedge notation,draw all the possible chiral isomers of compound 2.2 on each of your isomers assign the absolute stereochemistry as R or S for each chiral.Which Carbons are chiral? What is the absolute (R/S) configuration of the chiral carbon that IS NOT also part of a ring? Is it an R or S configuration? Show the priorities the using the structure below that led to this answer.The following molecules are: Hint: Build models and relate structures or perform a configurational assignment for each asymmetric center. They are identical if they are both "S" configured. They are identical if they are both "R" configured. They are enantiomers if one is "R" configured and the other is "S" configured.
- Construct a model of methane (CH4) using MolView and answer the following: Can it be superimposed on its mirror image? (Y/N) Does methane contain a plane of symmetry? (Y/N) Is methane chiral? (Y/N)Assign R and S to all of the asymmetric centers in the following molecules.The following are drawing of various co-workers of several different stereoisomers.5a. Pick one drawing, circle it and all confirmed drawings of that same stereoisomers.B. Pick a drawing that is not already circled and repeat for the new stereo isomers but box in with squares. C. Repeat for the third stereo isomer but with triangles.Also solve 5b and 5c .