dentify the stereocenters in each of the following molecules as R/S or achira f required, the same answer can be used more than once. i.e. there may be t somers or "S" isomers, etc.) Choose carefully. H - CH3 1. Risomer 2. Sisomer но 3. achiral molecule H2N > >
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- Identify the stereocenters in each of the following molecules as R/S or achiral. (Note if required, the same answer can be used more than once. i.e. there may be two "R" isomers or "S" isomers, etc.) Choose carefully. F CH3 1. Risomer H. 2. Sisomer ÓMe 3. achiral molecule (H3C)2HC. CH2CH3 HN H >the stereocenter labelled in blue has an a. R absolute configuration b. S absolute configuration1. Determine the R/S configuration of all stereocenters in the following molecules: CH3 F а 'ОН H IF S IF H .... ОН ОН F I ОН H ОН F CI CH3
- Identify the stereocenters in each of the following molecules as R/S or achiral. (Note if required, the same answer can be used more than once. i.e. there may be two "R" isomers or "S" isomers, etc.) Choose carefully. CH,CH, H+NH, CH(CH32 1. Risomer Br. OH 2. Sisomer 3. achiral molecule MeQ.3 For the following molecule, draw all stereoisomers and identify all pairs of enantiomers and diastereomers. Q. 4. Circle all the stereocenters in the following molecules. For each stereocenter, assign an R or S designation according to the standard rules CI, H H OH H3C... O: N. НО I... ן ייייייQ. 4. Circle all the stereocenters in the following molecules. For each stereocenter, assign an R or S designation according to the standard rules CI, H H3C., N. НО I.. 1ייייי' O....
- If attached to a stereocenter, which of the following groups would have the highest priority with respect to determining whether the configuration for the stereocenter is R or S? a. -CH2OH b.-NH2 c. (attached image)capacity. How many stereocentres does the molecule contain? H .N. *H,N N. Select one: O a. one O b. two O c. three O d. four O e. noneWhich compounds contain stereocentres? I. III. Select one: II, IV a. O b. I, II О с. I, III O d. III, IV ОН II. IV. ОН CI ОН
- HO H. a) Provide the R-S configuration for each of the following chiral centres. b) Provide the drawing and R-S configuration for one diastereomer of the above molecule. c) Bonus: Come up with a molecule that is a constitutional isomer of the above molecule and has the same amount of chirality centres and R-S configurations. For example: if the above molecule has 10 R and 10 S chiral centres, provide a constitutional isomer that also has 10 R and 10 S chiral centres.0. 4. Circle all the stereocenters in the following molecules. For each stereocenter, assign an R or S designation according to the standard rules OH H3C., НО2. For the following molecule, an anti-anxiety molecule marketed for organic chemistry students, circle all stereocenters and determine R or S configuration for all that is possible to do SO. CI CI Excess NaOH then HCI recrystallized OH OH OHI CI CI NOT THIS Actual product (your prediction)