(a) Draw a Lewis structure for the ozone molecule, \(\mathrm{O}_{3}\). (The
order of atom attachment is \(\mathrm{O}-\mathrm{O}-\mathrm{O}\), and they do
not form a ring.) Chemists use ozone to cleave carboncarbon double bonds
(Section 6.5C).
(b) Draw four contributing resonance structures; include formal charges.
(c) How does the resonance model account for the fact that the length of each
\(\mathrm{O}-\mathrm{O}\) bond in ozone \((128 \mathrm{pm})\) is shorter than the
\(\mathrm{O}-\mathrm{O}\) single bond in hydrogen peroxide (HOOH, \(147
\mathrm{pm}\) ) but longer than the \(\mathrm{O}-\mathrm{O}\) double bond in the
oxygen molecule \((123 \mathrm{pm})\) ?