Convert the following ring structures back into their Fischer projections: CH₂-OH CH₂-OH H H OH OH OH OH -1. H H H OH H Он OH I- Н エー -I Н OH Н OH ↑ Drag n' Drop here or Browse I
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- Lithocholic acid is an A–B cis steroid found in human bile. Draw lithocholic acid showing chair conformations, as in Figure 27-11, and tell whether the hydroxyl group at C3 is axial or equatorial.Can you help me sort these into Chiral and Achiral categories?Based on the image. What is 1. The anti-conformer of hexane in Newman projection. 2. The equivalent structure of LAM in sawhorse representation. 3.
- Draw all possible configurational stereoisomers for the given molecule below. Designate the R/S on the stereogenic centers and E/Z on the C=CDraw the Fischer, the Haworth, and the most stable chair conformation (equatorial vs axial) of β-D-mannose. Please number your carbons. Please draw it by hand and not by the internet through screen shot. Please explain. Thank you!Draw (2S, 3R)-2-bromo-3-chloropentane on the Fischer projection shown below.
- Draw each compound in its most symmetric conformation, star (*) any asymmetric carbon atoms, and draw any mirror planes.Label any meso compounds. You may use Fischer projections if you prefer.(a) (2R,3S)-2-bromo-3-chlorobutaneFor each pair, indicate whether they are constitutional isomers, enantiomers, diastereoisomers, or identical molecules. A BDEF(a) (S)-2-chlorobutane, draw any enantiomer.
- In a fischer projection, is the molecule r or s, and what is the highest priority?Locate the stereogenic centers in the attached Newman projection and labeleach center as R or S.Draw all possible stereoisomers for the molecule in Fischer projection and label the srelationship between each of the isomer.
