The heat of combustion of naphthalene $(C_{10}H_8(s))$ at constant volume is $-5133 \, kJ \, mol^{-1}$. The value of enthalpy change is .... $J$ $(R = 8.314 \, J \, K^{-1} \, mol^{-1}, T = 298 \, K)$.

The combustion of one mole of benzene takes place at $298 \, K$ and $1 \, atm$. After combustion,$CO_{2(g)}$ and $H_2O_{(l)}$ are produced and $3267.0 \, kJ$ of heat is liberated. Calculate the standard enthalpy of formation,$\Delta_f H^{\ominus}$ of benzene. Standard enthalpies of formation of $CO_{2(g)}$ and $H_2O_{(l)}$ are $-393.5 \, kJ \, mol^{-1}$ and $-285.83 \, kJ \, mol^{-1}$ respectively.

For the reaction $2C_6H_6(l) + 15O_2(g) \rightarrow 12CO_2(g) + 6H_2O(l)$ at $25 \ ^\circ C$,calculate the difference between the heat of reaction at constant volume and constant pressure in $kJ$.

Match the following columns:

Column $I$	Column $II$
$(a)$ Adiabatic process	$(1)$ Heat
$(b)$ Isolated system	$(2)$ Constant volume
$(c)$ Isothermal change	$(3)$ First law of thermodynamics
$(d)$ Path function	$(4)$ No exchange of matter and energy
$(e)$ State function	$(5)$ No heat exchange
$(f)$ $\Delta U = q$	$(6)$ Constant temperature
$(g)$ Law of conservation of energy	$(7)$ Internal energy
$(h)$ Reversible process	$(8)$ $p_{ext} = 0$
$(i)$ Free expansion	$(9)$ Constant pressure
$(j)$ $\Delta H = q$	$(10)$ Infinitely slow process involving equilibrium states
$(k)$ Intensive property	$(11)$ Entropy
$(l)$ Extensive property	$(12)$ Pressure
	$(13)$ Specific heat

Match the transformations in Column-$I$ with the appropriate options in Column-$II$.

Column-$I$	Column-$II$
$(A) \; CO_{2(s)} \to CO_{2(g)}$	$(p) \; \text{Transition state}$
$(B) \; CaCO_{3(s)} \to CaO_{(s)} + CO_{2(g)}$	$(q) \; \text{Allotropic change}$
$(C) \; 2H^{\cdot} \to H_{2(g)}$	$(r) \; \Delta H > 0$
$(D) \; P_{\text{(white solid)}} \to P_{\text{(red solid)}}$	$(s) \; \Delta S > 0$
	$(t) \; \Delta S < 0$

The entropy versus temperature plot for phases $\alpha$ and $\beta$ at $1 \ bar$ pressure is given. $S_T$ and $S_0$ are entropies of the phases at temperatures $T$ and $0 \ K$,respectively.
The transition temperature for $\alpha$ to $\beta$ phase change is $600 \ K$ and $C_{p, \beta} - C_{p, \alpha} = 1 \ J \ mol^{-1} \ K^{-1}$. Assume $(C_{p, \beta} - C_{p, \alpha})$ is independent of temperature in the range of $200$ to $700 \ K$. $C_{p, \alpha}$ and $C_{p, \beta}$ are heat capacities of $\alpha$ and $\beta$ phases,respectively.
$(1)$ The value of entropy change,$S_{\beta} - S_{\alpha}$ (in $J \ mol^{-1} \ K^{-1}$),at $300 \ K$ is. . . . . . .
$(2)$ The value of enthalpy change,$H_{\beta} - H_{\alpha}$ (in $J \ mol^{-1}$),at $300 \ K$ is.
[Use : $\ln 2 = 0.69$,Given : $S_{\beta} - S_{\alpha} = 0$ at $0 \ K$]