1) Draw an energy diagram for the rotation about the bond depicted in red in the molecule shown below. Draw Newman projections for each local maximum or local minimum energy. Explain your reasoning behind the relative energies depicted in your diagram.
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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?Using a Newman projections, draw all staggered and eclipsed confirmations that result from rotation around the indicated bond in each moleculea. 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.
- Draw the potential energy of the molecule circled at the top. Draw the other 3 Newman projections based on the one already drawn by rotating the back carbon clockwise. Explain your answersPlease 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?What would a newman projection look like for A, B, and C
- Draw the perspective structure, including all hydrogens, of the Newman projection in the picture. Thanks!Observe 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.Finish each Newman Projection to represent the given
- What is more stable in the newman projection a & 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.In each case below, draw a Newman projection as viewed from the angle indicated: