3. In the space below, draw the Newman Projection for Compound C with C1 and C3 in front (view down C3-Ca and C1-Ce parallel bonds). Br 5 CI 6 1 Br 3 2 3 4 Compound C CI
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How do you create a Newman projection that looks down both the c3-c4 and the c1-c6 bonds at the same time?
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- Please refer to the Newman projections shown below to when answering questions (a) – (f)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.Draw the highest and lowest energy Newman projection for 2- bromo-2,3-dimethylpentane when looking down C1-C2, C2-C3, C3-C4, C4-C5 bonds.
- 1. Draw structures of the most stable Newman projection for the image below2. Draw the five constitutional isomers having the molecular formula C4H6a) 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.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
- 1.1 Build a model for line structure and use the template given to draw a Newman projection for this conformation of the compound when viewed along the C2-C3 bond. (template given in second photo) 1.2 why is this the most stable structure?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?Rank the following Newman projections in order of increasing energy.
- Then draw the most stable and least stable Newman projection conformation from the C4-C5 bond in the molecule above. Draw the two most stable Newman projections of 3-methylpentane by viewing along the C2-C3 bond.Draw the most and least stable Newman projections for the following molecules ( focus on C2 and C3). a. 2-chloro-2- fluoropentane b. 2,2-dimethylbutane C. 2-chloro-2-methylpentane d. 1,2-dibromoethane