11) Draw the most stable and least stable conformation of molecule 7 in the boxes below in a Newman projection, looking down bond 1 to bond 2 indicated in the drawing and the line-angle formula of your Newman projection in the box below it. molecule 7 a) Most stable conformation of molecule 7 b) Least stable conformation of molecule 7
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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.Assign the absolute configuration of all molecules. Draw the most stable conformer in Newman projects with respect to bond C2-C3; for both a) and b). Draw Fisher projections for all molecules. do in detail complete
- Draw one chair conformer of (1S,2R,4R)-4-chloro-2-methylcyclohexan-1-ol. Include all groups of the three stereocenters, but no other hydrogens.Then draw the most stable and least stable Newman projection conformation from the C4-C5 bond in the molecule aboveAssign the absolute configuration of all molecules. Draw the most stable conformer in Newman projects with respect to bond C2-C3; for both a) and b). Draw Fisher projections for all molecules.
- Imagine that this worksheet has sucked you the plane of the page, and you are now facing the indicated bond of the drawn molecule. a. Draw the six main Newman projections for the indicated bond: three eclipsed, three staggered. b. Label which conformers are eclipsed ands taggered.c. Identify the most and least stable conformer, and explain your reasoning.Draw 2-methyl-4-sec-butyl cyclohexane in its chair conformation. Then draw the same molecule after a chair flip has occurred. Furthermore, provide the Newman projection for the most stable conformation.translate the bond-line notation structure to the Newman projection by filling int the missing groups (A, B, C, D or E) on the lines in the Newman projection so they match the conformation given in the original structure. Circle if the conformation is a staggered or eclipsed.
- Draw the two chair conformations for cis-1,2-dimethylcyclohexane and label all positions clearly as equatorial and axial. Label the most stable and least stable conformation and explain the reasonDraw 2,4-dimethylhexane as a bond-line structure. Then, looking down the C3 – C4 bond, draw a Newman projection representation of the 1) lowest energy (most stable) and 2) highest energy (least stable) conformations.For 1,2-dichloroethane: a.Draw Newman projections for all eclipsed conformations formed by rotation from 0° to 360° about the carbon-carbon single bond. b.Which eclipsed conformation(s) has (have) the lowest energy? Which has (have) the highest energy? c.Which, if any, of these eclipsed conformations are related by reflection?