$\Delta H^o_f$ of water is $-285.5 \, kJ \, mol^{-1}$. If enthalpy of neutralisation of monoacidic strong base is $-57.3 \, kJ \, mol^{-1}$,$\Delta H^o_f$ of $OH^{-}$ ion will be.....$kJ \, mol^{-1}$

Given below are two statements:
Statement $I$: For an ideal gas, heat capacity at constant volume is always greater than the heat capacity at constant pressure.
Statement $II$: In a constant volume process, no work is produced and all the heat withdrawn goes into the chaotic motion and is reflected by a temperature increase of the ideal gas.

The heat of combustion of carbon to $CO_2$ is $-393.5 \text{ kJ/mol}$. The heat released upon formation of $35.2 \text{ g}$ of $CO_2$ from carbon and oxygen gas is

$A$ calorimeter contains $0.2 \ kg$ of water at $30^{\circ} C$. $0.1 \ kg$ of water at $60^{\circ} C$ is added to it,the mixture is well stirred and the resulting temperature is found to be $35^{\circ} C$. The water equivalent of the calorimeter is $:-$ (in $J / K$)

The molar heat capacity for an ideal gas at constant pressure is $20.785 \ J \ K^{-1} \ mol^{-1}$. The change in internal energy is $5000 \ J$ upon heating it from $300 \ K$ to $500 \ K$. The number of moles of the gas is [Nearest integer] (Given: $R = 8.314 \ J \ K^{-1} \ mol^{-1}$)

The heat change for the following reaction at $298 \ K$ and at constant pressure is $+ 7.3 \ kcal$. $A_2B_{(s)} \to 2A_{(s)} + 1/2 \ B_{2(g)}$,$\Delta H = + 7.3 \ kcal$. The heat change at constant volume would be