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Proiide a perspectiie drawing of the enantiomer of (2R,3S)-1,2,3-trichloropentane
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- 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).For the given ee values, calculate the percentage of each enantiomer present. Q: 90% eeWhat is the ee for each of the following mixtures of enantiomers A and B? 95% A and 5% B
- Draw the resonance of the folowing and explain the isomeres aroomaticity. 1. 1H-1,2,3-triazone2. 3H-1,2,3-triazone 3. 4H-1,2,3-triazoneConsider a solution made up of 90% R and 10% S. What is the enantiomeric excess (ee%) of the R enantiomer?What is the structure's enantiomer. What are the structure's absolute configuration and its enantiomer's configuration?
- (b) (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 are enantiomers, diastereomers and meso compounds (if any).What is configuration (R or S) for the centers and the enantiomer for the whole isomer? Also tell if they are Z or E.6. Determine whether each compound is chiral or achiral. select the single best answer for each part.
- Identify the unique pairs of enantiomers and find any diastereomers.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)Tell whether each of the compounds below is achiral (A), chiral (C) or meso (M).