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Q: Using Fischer projection, draw all the stereoisomers of 3-chloro-2-hydroxypentanoic acid. ii)…
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- Draw examples of the following: (a) A meso compound with the formula C8H18 (b) A meso compound with the formula C9H20 (c) A compound with two chirality centers, one R and the otherAllenes are compounds with adjacent carbon-carbon double bonds. Many allenes are chiral, even though they don’t contain chirality centers. Mycomycin, for example, a naturally occurring antibiotic isolated from the bacterium Nocardia acidophilus, is chiral and has [α]D = -130. Explain why mycomycin is chiral.A) Please indicate the following compounds as chiral or achiral. B) Find 3 chiral centers and label them R or S
- Assign R or S configuration to each chirality center in thefollowing molecules, Identify which pairs are enantiomers ordiastereomers1. What is the relationship between the following two compounds? a.stereoisomersb.identicalc.constitutional isomers 2. Assign the absolute configuration of the chirality center as R or S.Salinosporamide A, isolated from a microbe called Salinispora tropica has shown promise as an inhibitor of cancer cell growth. Select the chiral centers in the following structure; the selected centers will appear highlighted green.
- 1.) Identify all chiral centers, then characterize them by R or S configuration 2.) Draw the enantiomer Was not sure if the Nitrogen with the question mark was a chiral center or not. Thank you!A Fischer projection of a molecule with one chiral center represented by a dot is shown below. Determine the R- or S-designation of this chiral center. A) R B) S C) no chiral center1. An object is chiral if it A. is superimposable on its mirror image B. is not superimposable on its mirror image C. has no mirror image D. is identical to each mirror image of itself
- Assign R/S to each of the chirality centers shown below.Provide stereochemical information (R or S for each chiral center)3b) (i) Using Fischer projection, draw all the stereoisomers of 3-chloro-2-hydroxypentanoic acid. ii) Assign the chiral centre(s) with R/S configurations in part (b)(i). Indicate which areenantiomers, diastereomers and meso compounds (if any).
