The standard enthalpy change for a reaction can be calculated using the following equation:
\[
\Delta_r H^\circ = \sum (\Delta_f H^\circ { products}) - \sum (\Delta_f H^\circ { reactants})
\]
From the problem statement, we know the standard enthalpy change for the reaction is \( +131.3 \, {kJ mol}^{-1} \). The given values are:
- \( \Delta_f H^\circ ({CO (g)}) = -110.5 \, {kJ mol}^{-1} \)
- \( \Delta_f H^\circ ({H}_2 ({g})) = 0.0 \, {kJ mol}^{-1} \) (since \( {H}_2 \) is in its standard state)
Substituting the values into the equation:
\[
131.3 = \left[ (-110.5) + (0.0) \right] - \left[ \Delta_f H^\circ ({C(graphite)}) + \Delta_f H^\circ ({H}_2{O (g)}) \right]
\]
Since the standard enthalpy of formation of graphite is zero:
\[
131.3 = (-110.5) - \Delta_f H^\circ ({H}_2{O (g)})
\]
Solving for \( \Delta_f H^\circ ({H}_2{O (g)}) \):
\[
\Delta_f H^\circ ({H}_2{O (g)}) = -241.8 \, {kJ mol}^{-1}
\]
Thus, the value of \( \Delta_f H^\circ \) for {H}_2{O} (g) is \( -241.8 \, {kJ mol}^{-1} \).