Draw the highest energy chair conformation when methyls1,3,and 5 are trans and when they are cis. Are there 1,3 diaxial interactions in the above models, Show by drawing.
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- Draw Newman Projections representing the two highest and two lowest energy conformers of (3S, 4S )-4-tert-butyl-2,3-dimethyloctane as viewed along the C3-C4 bond. b.) Label each conformer with theappropriate description then analyze them and rank their energies and explain your reasoning by specifyingthe types of interactions. (Hint: Draw the first and then rotate only the front or back carbon)Give typed full explanation otherwise leave itIn each case below, identify the higest and lowest energy conformations. In cases where two or three conformations are degenerate, choose only one as your anwser. Use Me, H, and Et when drawing the structures.
- | Which of the following compounds is more stable? To get credit you must draw the most stable chair conformation of each compound and explain your answer.Please explain me this question.F) Circle the letter corresponding to the relationship of each pair of structures: Identical (1), Conformers (C), Enantiomers (E) (enantiomers can have different conformations). FIRST... determine the absolute configuration of chiral centers. I OH с OH E