Draw Fischer projection and line/wedge diagrams for the two enantiomers of usnic acid.
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Draw Fischer projection and line/wedge diagrams for the two enantiomers of usnic acid.
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
Translate the following wedge-and-hashed structure to its Fischer projection. Translate the following wedge-and-hashed structure to its Fischer projection. The carbon backbone has been predrawn. Complete the Fischer projection. Note: If you place the hydroxy group on the left side of the Fischer projection, be sure to select "HO" instead of "OH". CH3 Hс, он OH Br HO CH3 CH3
oints): Draw a correct wedge/dash drawing of the following Fischer projection І ОН -он І І он І -он
Translate the following wedge-and-hashed structure to its Fischer projection. Translate the following wedge-and-hashed structure to its Fischer projection. The carbon backbone has been predrawn. Complete the Fischer projection. Note: If you place the hydroxy group on the left side of the Fischer projection, be sure to select "HO" instead of "OH". CH3 Holm OH - — но нас I CH3 CH3
Did I draw the wedge/dash drawing correctly? Da Convert the following Fischer projection into a to wedge/ dash drawings cd tv CH3 70 noita o vinduisol bod autxin العمال المنهل علي ابن HO LOCH Sky was t = 0 og do do CH3
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.
1. a. (4 points) Draw the dash-wedge structure of (2R,3.5)-2,3-dichloropentane. b. (4 points) Draw the Fischer projection of enantionmer 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 diastercomers 2. (6 points) Draw the mechanisms of the propagation steps of the reaction shown, focusing on the formation of the major product(s). NBS
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.
Draw the correct fischer projection of each amino acid as it would appear at ph 1 a) L-histidine b) L- glutamic acid c) D-glutamine d) D-lysine
Convert the line structures to Fischer diagrams. 3. Convert the line structures below to Fischer diagrams OH OH он о он но но OH OH O OH OH