3. In the box provided, draw the lowest energy Newman projection (looking down the bond indicated) that corresponds to the compound drawn. (4 points total, 2 points per box) a) b)
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- 4) Draw the most stable and least stable Newman projections of the following compound viewed along the indicated bond. Br HObserve the Newman projection of the next molecule along the bond shown in red with the front carbon the one bonded to "Cl". a) Draw one of the Newman projections of the molecule with a staggered conformation. b) Draw one of the Newman projections of the molecule with an eclipsed conformation.C Draw the most stable Newman projection for each of the labeled C-C bonds: ...... A A .D D B
- Draw the lowest energy Newman projection of the molecule on the left looking down the bond indicated for molecule A. For molecules B and C, draw the lowest energy chair conformations.4. Draw a Newman projection of the following compound that centers along the marked bond. This one! CH3 CH3 + + Hdraw newman projection for the indicated bond. put largest groups anti to each other.
- 6. How many stereoisomers total are possible for each compound below appropriate line). a. b. Br Br Br place answer on theanswer c and d pleasea) Draw a Newmann Projection of the following compound looking down the indicated bond (Ph represents a benzene ring). Br b) Using a Newmann Projection draw a conformation of this molecule where the bromine and hydrogen are in an anti-conformation
- a. 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.Show your all work) Draw the most stable Newman projection of each molecule along the bond indicated by the arow. Use one template in each case. Briefly (< 10 words) explain your choices. H. HN