The standard enthalpies of formation of ions in aqueous solutions are obtained
by arbitrarily assigning a value of zero to \(\mathrm{H}^{+}\) ions; that is,
\(\Delta H_{\mathrm{f}}^{\circ}\left[\mathrm{H}^{+}(a q)\right]=0\)
(a) For the following reaction
$$\begin{array}{r}\mathrm{HCl}(g) \stackrel{\mathrm{H}_{2}
\mathrm{O}}{\longrightarrow} \mathrm{H}^{+}(aq)+\mathrm{Cl}^{-}(a q)
\\\\\Delta H^{\circ}=-74.9 \mathrm{~kJ} / \mathrm{mol}\end{array}$$
calculate \(\Delta H_{\mathrm{f}}^{\circ}\) for the \(\mathrm{Cl}^{-}\) ions.
(b) Given that \(\Delta H_{\mathrm{f}}^{\circ}\) for \(\mathrm{OH}^{-}\) ions is
\(-229.6 \mathrm{~kJ} / \mathrm{mol}\), calculate the enthalpy of neutralization
when 1 mole of a strong monoprotic acid (such as \(\mathrm{HCl}\) ) is titrated
by 1 mole of a strong base (such as \(\mathrm{KOH}\) ) at \(25^{\circ}
\mathrm{C}\).