Given reaction (at 298 K):
NH2CN(s) + 3/2O2(g) -> N2(g) + CO2(g) + H2O(l)
\[ \Delta U = -742.7\ \text{kJ mol}^{-1} \quad \text{at } 298\ \text{K} \]
Relation between ΔH and ΔU (at constant T):
\[ \Delta H = \Delta U + \Delta n_g \, R T \] where \(\Delta n_g\) = (moles of gaseous products) − (moles of gaseous reactants).
Step 1: Calculate Δng
Gaseous species:
\[ \Delta n_g = 2 - \tfrac{3}{2} = \tfrac{1}{2} = 0.5 \]
Step 2: Use ΔH = ΔU + ΔngRT
Use \(R = 8.314\ \text{J K}^{-1}\text{mol}^{-1}\), \(T = 298\ \text{K}\):
\[ \Delta H = -742.7\ \text{kJ mol}^{-1} + 0.5 \times 8.314\ \text{J K}^{-1}\text{mol}^{-1} \times 298\ \text{K} \] Convert the correction term to kJ: \[ 0.5 \times 8.314 \times 298 \approx 1238.7\ \text{J mol}^{-1} \approx 1.24\ \text{kJ mol}^{-1} \] \[ \Delta H \approx -742.7\ \text{kJ mol}^{-1} + 1.24\ \text{kJ mol}^{-1} \approx -741.5\ \text{kJ mol}^{-1} \]
The enthalpy change for the reaction at 298 K is approximately \[ \boxed{\Delta H \approx -7.42 \times 10^{2}\ \text{kJ mol}^{-1}} \] (about \(-741.5\ \text{kJ mol}^{-1}\)).