Draw (2R, 3S) 2-bromopentan-1.3-diol in a Fischer projection.
Drag the appropriate labels to their respective targets
Draw the Fischer projection for the oxidation product of D-xylose. Drag the appropriate labels to their respective targets. Part C Draw the Fischer projection for the reduction products of D-xylose.Drag the appropriate labels to their respective targets. Part A Assign all of the chiral carbon atoms in the following molecule to (1).
2.Draw a Newman projection, a wedge-dash structure and a Fischer projection for all four stereoisomers of 2-bromo-3-chlorobutane. The wedge dash structure is given for part a – all you need to do is finish the Newman projection and the Fischer projection. a.2R, 3R. On each structure show how you determined where each group goes. (part a only) b.2S,3S c.2S, 3R d.2R, 3S CH3 Brci CH CH3
draw the fisher projection of 2R, 3R) 2,3-dibromopentane 2S, 3S) 2,3-dibromopentane 2R, 3S) 2,3-dibromopentane 2S, 3R) 2,3-dibromopentane
1. a. (4 points) Draw the dash-wedge structure of (2R,3S)-2,3-dichloropentane. b. (4 points) Draw the Fischer projection of enantiomer of the compound drawn in part a. Name the enantiomers. c. (6 points) Draw the Newman projections (looking down the C2-C3 bonds) of the diastereomers of the compound drawn in part b. Name the diastereomers.
Can someone please help me draw the Fischer projection for (2R,4S) methyl-4-amino-4-chloro-2-methoxypentanoate? I understand the nomenclature and process on how to draw a Fischer projection, but I am stuck on where to draw the CH2 between both chiral centers. Thank you!
show all steps of these synthesis problems (2S,3S)-2,3-hexanediol (a diol has two -OH groups) (33) acetylene Br + En (35) (2R,3S)-2,3-hexanediol (a diol has two -OH groups) (36) Br Он (37) + En он Cl (39) (40) (2S,3S)-2,3-hexanediol (a diol has two -OH groups) (33) acetylene Br + En (35) (2R,3S)-2,3-hexanediol (a diol has two -OH groups) (36) Br Он (37) + En он Cl (39) (40)
Draw the Fischer projection for the monosaccharide drawn as a haworth projection below. Draw the Fischer projection for the monosaccharide drawn as a Haworth projection below. Switch between an aldose and a ketose by clicking on "switch carbonyl group." Add or delete carbon atoms using the add ("+") or delete ("x") buttons. Clicking on a blue box once adds a hydrogen atom (H). Clicking on a blue box again toggles between H and OH.
M UUR Onepel U Drawing Fischer Projections of Monosaccharides Part C For the structure on the right, add either H or 0-H to create the enantiomer of the structure on the left. Drag the appropriate labels to their respective targets. ► View Available Hint(s) Reset Help H- | H O OH I 애 * dood OOOO I 애 I ОН OH Vaatcilarides Part D For the structure on the right, add either H or 0-H to create the enantiomer of...
The skeletal structure of D-fructose, a carbohydrate with three asymmetric centers, is provided below. Skeletal structure of D-fructose OH OH OH HO OH Add either an H or OH group to complete the Fischer projection for D-fructose. Drag the appropriate labels to their respective targets. Hints CH,OH 2 OH CH2OH
Drag and drop the appropriate labels to show the correct Fischer projection for L-alanine. Make sure the "crosshairs" circle at the upper left corner of each label is more or less centered on the appropriate blue dot. COOH CH, CHA SH H NH HEN NH CH2OH |H₂N| CH,SH OH