Reaction:
N2O4(g) + 3 CO(g) -> N2O(g) + 3 CO2(g)}
Given standard enthalpies of formation (in kJ mol\(^{-1}\)):
Use:
\[ \Delta_r H^\circ = \sum \nu_p \Delta_f H^\circ(\text{products}) - \sum \nu_r \Delta_f H^\circ(\text{reactants}) \]
Sum for products:
\[ \Delta_f H^\circ(\ce{N2O}) + 3\,\Delta_f H^\circ(\ce{CO2}) = 81 + 3(-393) = 81 - 1179 = -1098\ \text{kJ} \]
Sum for reactants:
\[ \Delta_f H^\circ(\ce{N2O4}) + 3\,\Delta_f H^\circ(\ce
\(∆_rH\) for a reaction is defined as the difference between \(∆_fH\) value of products and \(∆_fH\) value of reactants.
\(△_rH\) =\(Σ△_fH\) (product) - \(Σ△_fH\) (reactants)
For the given reaction,
\(N_2O_4(g) + 3CO(g) → N_2O(g) + 3CO_2(g)\)
\(△_rH\) = \(△_fH (NO_2)\)+ \(3△_fH (CO_2)\) - \(△_fH (N_2O_4)\) + \(3△_fH (CO)\)
Substituting the values of \(∆_fH\) for \(N_2O, CO_2, N_2O_4,\) and \(CO\) from the question, we get:
\(△_rH = [{81\ kJ mol^{-1} + 3(-393)\ kJ mol^{-1}} - {9.7\ kJ mol^{-1} + 3(-110)\ kJ mol^{-1}}]\)
\(△_rH = -777.7\ kJ mol^{-1}\)
Hence, the value of \(∆_r H\) for the reaction is \(-777.7\ kJ mol^{-1}\).
{CO}) = 9.7 + 3(-110) = 9.7 - 330 = -320.3\ \text{kJ} \]
Reaction enthalpy:
\[ \Delta_r H^\circ = -1098 - (-320.3) = -1098 + 320.3 = -777.7\ \text{kJ} \approx -7.78 \times 10^{2}\ \text{kJ} \]
\[ \boxed{\Delta_r H^\circ \approx -7.8 \times 10^{2}\ \text{kJ}} \] (The reaction is highly exothermic.)