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- (a) Draw the most stable chair conformers of trans-1,3-diisopropylcyclohexane and trans-1,4-diisopropylcyclohexane. (b) Which is more stable: trans-1,3-diisopropylcyclohexane or trans-1,4-diisopropylcyclohexane?Fill in the blanks: cis-1,3-Dimethylcyclohexane has two different chair conformations: one withboth methyl groups in __________ positions and one with both methyl groups in ____________ positions.Draw the two chair conformations for t-butyl-cyclohexane and explain which is the most stable
- Draw the alternative chair conformation of this compound. Of the two chair conformations, which is more stable?Draw 5 Chair Conformations of Cyclohexane with right side pointing up and 5 with the left side pointing up.H C-Ć- C -CI Following is the structural formula of 1,2– dichloroethane. H H a) Draw Newman projections for all staggered and eclipsed conformations formed by rotation from 0° to 360° about the carbon- carbon single bond. b) Which staggered conformation(s) has the lowest energy; which has the highest energy? c) Which eclipsed conformation(s) has the lowest energy which has the highest energy?
- Draw the two chair conformations of cis-1-tert-butyl-2-ethylcyclohexane, which one is most stable.draw the 2 chair conformations of trans-1-bromo-3-isopropylcyclohexaneUse a Newman projection about the indicated bond to draw the most stable conformer for each compound. (a) 3-methylpentane about the C2¬C3 bond