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- 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 ve constitutional isomers having molecular formula C6H14.Draw 5 Chair Conformations of Cyclohexane with right side pointing up and 5 with the left side pointing up.
- Use a Newman projection about the indicated bond to draw the most stable conformer for each compound. (a) 3-methylpentane about the C2¬C3 bondDraw the sawhorse projection of most stable conformer of 1-isopropyl-3-methycyclohexaneLooking alongC1−C2andC4−C5bonds, draw a Newman projection for each of the two chair conformations of trans 1,2-dimethylcyclohexane.
- Draw the structures of the two chair conformations of trans-1-tert-butyl-4-ethylcyclohexane. Which conformation is more stable? Explain your answer.Which staggered conformation(s) has (have) the lowest energy? Which has (have) the highest energy?Draw and name all constitutional isomers of a compound having the molecular formula C4H8O2
- Explain following question ❓Draw the two possible ring puckers for trans-1,3-dimethylcyclobutane. Which of the two conformers is most stable? Why?(c)Conformational isomer is the different spatial arrangement of the atoms that resulted from rotation about a single bond. (i) Differentiate anti conformers and gauche conformers (ii) Using a newman projection, draw the anti conformer and gauche conformers of 3,3-dimethylheptane (viewed along the C3-C4 bond)