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- Consider the Newman projection below. a. Draw a full Lewis structure of this molecule with R1=Me,R2=Et , and R3=iPr . b. Given the sizes of these R groups (R3R2R1) , does the Newman projection above show thelowest potential energy conformation of this bond? If not, draw a Newman projectionshowing the lowest P.E. conformation (sighting down this same bond). c. To draw a Newman projection in the lowest P.E. conformation, the following rule of thumbusually applies: Place the largest group on the front carbon anti to the largest group on theback carbon. Is your answer to the previous question consistent with this rule of thumb?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.Draw both a chair confirmation of the substitutes cyclohexane drawn below. Be certain to actually do a ring flip. Also be certain to very clearly distinguish axial from equatorial positions. Then circle the more stable conformation.
- 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.For the following Newman Projection, determine whether it is in the lowest energy conformation as drawn. Then, fill in the Newman Projection for the lowest energy conformation. You may use the table of A-values provided in the instructions to determine the correct answer. 2. [Select] 3. [Select] 4. [Select] Is this the lowest energy conformation? [Select] For each number on the partially filled Newman Projection above, select the group that would make the lowest energy conformation. 1. [Select] 5. OH [ Select] 3 -@ CH3For the following conformer, draw a Newman projection looking down the 1,2 (red) bond.
- Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed down the red bond in the direction of the red arrow. Your projection should be oriented as shown by the arrow marked up. So the CH2SH group on the front carbon should be above the H and H3C groups, no matter which template you useObserve 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.Draw both chair confirmations of the substituted cyclohexane drawn below. Be certain to actually do a ring flip. Also be certain to very clearly distinguish axial from equatorial positions. Then circle the more stable conformation. Draw a planar representation of a stereoisomers which would have a higher heat of combustion and lower heat of combustion.
- Draw the Newman projections for the most and least stable conformations and indicate what strain(s) the least stable conformation has. Look in the direction of arrow.draw the newman projection looking down the indicated bond, and then draw the most stable and least stable conformation...Draw the Newman projections for the eclipsed conformations for the indicated C-C bond. The included arrow shows by what perspective (i.e., which carbon is in front) you should draw the Newman. projection. Then select the highest energy conformation and provide an explanation for your selection. Ye