F and Cl are below the plane in wegde dash. so they will be on same side in newman projection..
SH and OH are above the plane in wegde dash .so they will be on same side in newman projection..
Br and H was anti and on the plane in wegde dash..
it will be anti in newman projection.8
Map Translate the given theoretical conformer from the wedge-and-dash drawing into its Newman projection. HSB HS...
1) 2) 3) Translate the given theoretical conformer from the Newman projection to its wedge-and-dash drawing. (Replace the provided placeholder H atoms with the appropriate atom/group). Translate the given theoretical conformer from the wedge-and-dash drawing into its Newman projection. Translate the given conformer from the wedge-and-dash drawing into its Newman projection. Select the correct Newman projection below, and drag the three groups (CI, Br, and CH3) to their correct locations.
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
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
2. Draw a wedge and dash structure of the following Newman projection. OCX , ITI Ž Draw a wedge and dash structure of the following Newman projection. CH3 HTCH3 CH3 H Ėt
how to draw wedge dash structure and newman projection for C2-C3 bond for 3-bromo-2,2,3-trichloro-1-fluorobutane
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
(1 pt) Convert the following dash/wedge structure into Newman projection (use the eye for direction viewed). Br CH3 H2N (2 pts) Convert each of the following Newman projections into dash/wedge structures. CH2CHs CH2OH cl CH20H 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
3. Draw butane in wedge and dash depiction, sawhorse depiction and in its Newman projection looking down the 2.3 bond. Show eclipsed, gauche and anti forms. 4. Draw all Newman projections of 2-methylhexane showing eclipsed, gauche and anti forms. Rotate about the 3.4 carbon-carbon bond and watch what happens to the Draw a potential energy diagram for the rotation about the 3,4 carbon- carbon bond plotting Potential Energy versus Torsion Angle.
Gei heip answering MoTecuiar Drawing Draw a wedge-and-dash structure of the conformer of 3-heptyne that is analogous to anti-anti pentane. Explicitly draw out ALL hydrogen atoms. Edit