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- Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.2. Convert the following bond-line structure to Newman projections that represents it lowest energy and highest energy conformations. Look down the indicated C2-C3 bond. lowest energy highest energyHow do I draw the Newman projection for each line structure? This is for organic chemistry.
- Which is the correct newman projection for the following molecule (as drawn below assuming no rotation) when looking down the bond indicated by the arrow? 0 0 Me Me Et Me Me Et Me Me II….. H H H HSelect the correct molecular geometry and bond angles around the carbocation: |||||………. trigonal pyramidal, 120° tetrahedral, 109.5° O tetrahedral, 105° trigonal planar, 120° trigonal pyramidal, 109.5°Possible Newman projection for following?
- p. Is the molecule below conjugated? If so, circle the atoms that are part of the conjugation. Also indicate the orbital that each lone pair occupies. O-Q6 Relationship Determine the relationship between the following pairs of molecules. CH3 CH H3C, CH3 CH3 CH3 H3C" CH3 H;C ČH3 CH3 H;C H;C CH3 D. F5. Draw Newman projections for the following molecules as directed by the arrow. Br Br CI