Describing chair conformations of trans-dimethylcylcohexane

Question

Assignment:

Q1. Which of the following correctly lists the following isomeric alkanes in order of increasing boiling point? n-hexane, 2,3-dimethylbutane, 2-methylpentane

a. n-hexane < 2-methylpentane < 2,3- dimethylbutane
b. 2-methylpentane < 2,3-dimethylbutane < n-hexane
c. 2,3-dimethylbutane < 2-methylpentane < n-hexane
d. n-hexane < 2,3-dimethylbutane < 2-methylpentane

Q2. Which of the following statements about n-heptane is true?
a. It is non-polar and water soluble
b. It is polar and water soluble
c. It is polar and water insoluble
d. It is non-polar and water insoluble

Q3. The number of constitutional isomers that are alkanes that can be drawn for C₄H₈ is

Q4. Which compound would be expected to show the most strain per -CH₂- ?
a. n-hexane
b. cyclobutane
c. methylcyclopentane
d. ethylcyclopropane

Q5. Which of the statements below correctly describes the chair conformations of trans-1,2-dimethylcylcohexane?

a. The two chair conformations are identical in energy
b. The higher energy conformation contains one axial methyl and one equatorial methyl group
c. The lower energy conformation contains two axial methyl groups
d. The lower energy conformation contains two equatorial methyl groups.