Consider the following data :

Heat of formation of $\mathrm{CO}_2(\mathrm{g})=-393.5 \mathrm{~kJ} \mathrm{~mol}{ }^{-1}$

Heat of formation of $\mathrm{H}_2 \mathrm{O}(\mathrm{l})=-286.0 \mathrm{~kJ} \mathrm{~mol}{ }^{-1}$

Heat of combustion of benzene $=-3267.0 \mathrm{~kJ} \mathrm{~mol}^{-1}$

The heat of formation of benzene is __________ $\mathrm{kJ} \mathrm{mol}^{-1}$. (Nearest integer)

The formation enthalpies, $\Delta \mathrm{H}_{\mathrm{f}}^{\ominus}$ for $\mathrm{H}_{(\mathrm{g})}$ and $\mathrm{O}_{(\mathrm{g})}$ are 220.0 and $250.0 \mathrm{~kJ} \mathrm{~mol}^{-1}$, respectively, at 298.15 K , and $\Delta \mathrm{H}_{\mathrm{f}}^{\ominus}$ for $\mathrm{H}_2 \mathrm{O}_{(\mathrm{g})}$ is $-242.0 \mathrm{~kJ} \mathrm{~mol}^{-1}$ at the same temperature. The average bond enthalpy of the $\mathrm{O}-\mathrm{H}$ bond in water at 298.15 K is _______ $\mathrm{kJ} \mathrm{~mol}^{-1}$ (nearest integer).

Standard entropies of $\mathrm{X}_2, \mathrm{Y}_2$ and $\mathrm{XY}_5$ are 70, 50 and $110 \mathrm{~J} \mathrm{~K}^{-1} \mathrm{~mol}^{-1}$ respectively. The temperature in Kelvin at which the reaction

$$\frac{1}{2} \mathrm{X}_2+\frac{5}{2} \mathrm{Y}_2 \rightleftharpoons \mathrm{XY}_5 \Delta \mathrm{H}^{\ominus}=-35 \mathrm{~kJ} \mathrm{~mol}^{-1}$$

will be at equilibrium is __________ (Nearest integer)

The bond dissociation enthalpy of $\mathrm{X}_2 \Delta \mathrm{H}_{\text {bond }}^{\circ}$ calculated from the given data is ___________ $\mathrm{kJ} \mathrm{mol}^{-1}$. (Nearest integer)

$$\begin{aligned} & \mathrm{M}^{+} \mathrm{X}^{-}(\mathrm{s}) \rightarrow \mathrm{M}^{+}(\mathrm{g})+\mathrm{X}^{-}(\mathrm{g}) \Delta \mathrm{H}_{\text {lattice }}^{\circ}=800 \mathrm{~kJ} \mathrm{~mol}^{-1} \\ & \mathrm{M}(\mathrm{~s}) \rightarrow \mathrm{M}(\mathrm{~g}) \Delta \mathrm{H}_{\text {sub }}^{\circ}=100 \mathrm{~kJ} \mathrm{~mol}^{-1} \end{aligned}$$

$$\mathrm{M}(\mathrm{~g}) \rightarrow \mathrm{M}^{+}(\mathrm{g})+\mathrm{e}^{-}(\mathrm{g}) \Delta \mathrm{H}_{\mathrm{i}}^{\circ}=500 \mathrm{~kJ} \mathrm{~mol}^{-1}$$

$$\mathrm{X}(\mathrm{~g})+\mathrm{e}^{-}(\mathrm{g}) \rightarrow \mathrm{X}^{-}(\mathrm{g}) \Delta \mathrm{H}_{\mathrm{eg}}^{\circ}=-300 \mathrm{~kJ} \mathrm{~mol}^{-1}$$

$$\mathrm{M}(\mathrm{~s})+\frac{1}{2} \mathrm{X}_2(\mathrm{~g}) \rightarrow \mathrm{M}^{+} \mathrm{X}^{-}(\mathrm{s}) \Delta \mathrm{H}_f^{\circ}=-400 \mathrm{~kJ} \mathrm{~mol}^{-1}$$

[Given : $\mathrm{M}^{+} \mathrm{X}^{-}$is a pure ionic compound and X forms a diatomic molecule $\mathrm{X}_2$ in gaseous state]