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Q: Locate the stereogenic centers in each Newman projection and label each center as R or S.
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Can you help me draw R-1-bromo-2-chloropropane and it's Newman projection?
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- Can someone please explain why the least stable newman projection, with the arrow pointing to the CH3, why the CH3 goes there?Can you help me convert this into a Newman projection? Draw the most stable and least stable projections.Please help me draw these Newman projections, I have no idea what I'm doing. Please look down the red bond in the direction of the pointed arrow
- Draw a hexane chain that has 2 carbon substituents and 1 halogen. Translate this drawing to the most stable Newman projection.Draw the perspective structure, including all hydrogens, of the Newman projection in the picture. Thanks!Convert each representation to a Newman projection around the indicated bond.
- a) Sighting down the C3-C4 bond, draw the gauche (60 degrees) and anti (180 degrees) Newman projections of 2,4-dimethylhexane. b) Circle the conformation that you drew that is lower energy.Please look at the picture as it is related on my question. When do we decide that it is CH3 or H3C that we put while we are drawing the Newman projection?Focus only on carbon 1 For carbon 1, which group has the highest priority? a,b,c or d?why? What enantiomer is carbon 1? R or S?