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- NO Consider the molecule below: H₂C H3C CH₂CH3 CH₂CH3 Consider rotation around the indicated bond. [1] Draw a Newman projection for the lowest energy conformer of this molecule looking down the indicated bond. [2] Draw a Newman projection for the highest energy conformer of this molecule looking down the indicated bond. # 3 d F4 % 5 F6 00Translate the given theoretical conformer from the Newman projection to its wedge‑and‑dash drawing.2. Draw the Newman projection for the molecule below down the C3-C4 bond. CI F
- A. Draw the Newman projection for antistaggered conformer of 1,2-dichloroethane. B. Draw the Newman projection for Gauche-staggered conformer of 1,2-dichloroethane. C. Draw the Newman projection for any eclipsed conformer of 1,2-dichloroethane.Draw the most stable & least stable Newman projections for the following molecule. Use the indicated carbons as the front and back carbons in the Newman projection.A) Draw the corresponding Newman projections of each molecule below B) Determine if the Newman projection is in the most stable conformation. If it is not, rotate and redraw the Newman projection in its most stable form. Br پر F X "H де C3-C2 bond C3-C4 bond C2-C3 bond C3-C2 bond C2-C3 bond
- 2D Representations Conformation Newman Sawhorse projection projection 1. 2. preferred (most stable) chloroethane 3. 4. least stable 5. preferred (most stable) 1,2-dibromoethane 7. 8. least stable 6.10) Draw a Newman Projection along the C3-C4 for the molecule shown below. (C3 should be in front.) C3 C4 HO OHDraw the most stable Newman projection of the following moleculelooking along C2 and C3.
- Convert the following Newman projection into a dash-wedge 3-D drawing and convert the dash-wedge 3D drawing into a Newman projection.Draw the perspective form of the newman projection from the viewpoint indicated below by the arrowa. Draw the Newman projection for each molecule shown here, looking down the c-c bond indicated by the arrow. b. Which configuration do you think is more stable? Explain.
