(a) On catalytic hydrogenation, compound \(\mathrm{A}, \mathrm{C}_{5}
\mathrm{H}_{8}\), gave cis-1, 2-dimethy lcyclopropane. On this basis, three
isomeric structures were considered possible for \(\mathrm{A}\). What were they?
(b) Absence of infrared absorption at \(890 \mathrm{~cm}^{-1}\) made one of the
structures unlikely. Which one was it?
(c) The nmr spectrum of A showed signals at \(\delta 2.22\) and \(\delta\) \(1.04\)
with intensity ratio \(3: 1\). Which of the three structures in
(a) is consistent with this?
(d) The base peak in the mass spectrum was found at \(\mathrm{m} / \mathrm{e}
67\). What ion was this peak probably due to, and how do you account for its
abundance?
(e) Compound A was synthesized in one step from openchain compounds. How do
you think this was done?