uestions 1. Redraw the Newman projection inba Fischer projections using the template provided OH な. OH...
[8 pts] On the template provided below, draw the Newman projection of the correct enantiomer for the amino acid B-phenylalanine shown below. ge HON OH COOH
1. Use the following structure to draw Newman Projections (each subsequent projection with the back carbon rotated 60" clockwise), Label the projection that is highest in energy and lowest in energy. Explicitly label all H's and CHY's. The arrow denotes the "front" carbon. Use this position to start your first Newman Projection Hae H | 改改改改 2. Finish each Newman Projection to correctly represent the following molecule in the box. OH Br CH3 0月
Draw fischer projection 1. (a) Draw the Fisher projection f H CH2SH OH Br CH2SH CH3 HSH2 CH3 Br CH SH OH
1. (3 points) Complete the Newman projection for the compound shown. The bond to focus on is indicated, and a template is provided for you to complete. Draw the lowest energy conformation around the indicated bond. Do not invert the stereochemistry at stereogenic centers. 1. (3 points) Complete the Newman projection for the compound shown. The bond to focus on is indicated, and a template is provided for you to complete. Draw the lowest energy conformation around the indicated bond....
Given the following perspective drawing: H " HSH OH HỌC CHỊ Choose the Fischer projection, from the choices below, that is identical in constitution, configuration and conformation CH3 HO- Hs—+ エエーー H3C4H Нас # ### CH CH3 CH3 H HO— SH H CH3 Submit Answer Tries 0/1 Given the following perspective drawing: t-Bu If a Cr14年 QH Choose the Fischer projection, from the choices below, that is identical in constitution, configuration and conformation -Bu H1-CI HO— Br 一二 十 一F-Bu...
in Newman - Projection sale energy levels! H al Mé 4 Me tbuk 5) in Fisher-Projection! OH ICHO OH ८) - सल्लाने का Me in Natta projection! H Me H d) most stabled chair conformation in tBu -Me Me in Newman - Projection all energy levels! ## Mé ME ме tBuk 5 in Fischer - Projection! Ott CHO () to tester OH Me H projection! Me H H in Natta / for example IH Br in most stabled chair conformation...
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
what are the newman projection of the ring flip of these newman projections. thank you Name Lab Partner 12 Dimethylcyclerone CH3 CH₃ - Cir HN CH3 a la playable Trans Lab Parte 1, 4, dimethylcyclohexane -CH3 T CHS Trane CH3
Part C: In the boxes provided, indicate whether the carbon with the (*) is R or S. For the two compounds that have two stereocenters, label in the third box meso or not meso. Perspective Structures H NH2 CI Br, HO НО" H Cl CI CI Br Fischer Projections H Br CI OH CI Br OH HO H H F- Br SH Br Br CH3 CI 2 2 S2) Newman Projections Br Br * Br Br H H
1. Draw the Neman Projection of the following Promane descriptions Newman projection for most stable Newman projection for least stable conformation conformation 2. Draw the Newman projections for butane looking down the C2-C3 bond through a full 360 degree rotation. Start with the anti-staggered Newman projection then draw and label each Newman projection (staggered, eclipsed, gauche, anti-staggered, fully-eclipsed) for every 60 degrees of rotation Newman projection for most stable Newman projection for second-most stable conformation Conformation Newman projection for least...