Starting from the wedge-and-dash structure below (sighting down the indicated bond). Rotate only the back carbon to provide the anti staggered conformer. H3C HI!!! H H Ph H Drawing show work. don't give Ai generated solution
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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.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.6. Newman projections to Lewis structures From the following Newman projections, draw the corresponding Lewis structure in the same conformation. A) B) H. H CH3 H₂C N H OH CI Br CH3 H OH CH3
- Please help me with my conformations assignment! Thank you!!Consider rotation about the indicated bond in the molecule below. Which Newman Projection formula best represents the most stable conformer of the molecule with respect to rotation about the indicated bond? [As noted below: there is no steric strain between -H and -Et that have a gauche, staggered relationship] H CH3 Br-C-C-CH₂CH3 H. H Br CH₂CH₂ 1 CH3 H CH3CH₂ H Br H₂C || H H₂C H Br H ||| Select one: OA. I O B. II O C. III O D. All conformers have identical energies. CH₂CH3 H NOTE CH3CH₂ H no steric strainChoose either I, II, III, or IV
- help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all workingStarting from the structure below (sighting down the indicated bond). rotate the back carbon to provide an eclipsed conformer of the structure. Ph H H HI!!! ++||||4 CH₂CH3 I I I I I I H Draw Newman Projection I I II H. H H. H Identify the Newman projection that depicts the eclipsed conformation of butane. CH3 I H CH3 H CH3 H CH3 || IV `H I H H H CH3 H H V H3C CH3 J HH H CH3 H -H CH3 FH CH3 A) I B) II C) III D) IV E) V
- Sight along the C2 - C; bond of 2,3 -dimethylbutane, and draw a Newman projections for all the staggered and eclipsed conformation. Draw the expected potential energy diagram for this molecule. 2 3 4 ĈH3-CH2 – CH – CH3 CH3 CH3 2, 3 - dimethyl butanetranslate 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.Starting from the Newman projection below, rotate the back carbon to provide the structure in a gauge staggered conformation.