The amount of heat evolved when $500 \ cm^{3}$ of $0.1 \ M \ HCl$ is mixed with $200 \ cm^{3}$ of $0.2 \ M \ NaOH$ is (in $kJ$)

In a constant volume calorimeter,$3.5 \ g$ of a gas with molecular weight $28$ was burnt in excess oxygen at $298.0 \ K$. The temperature of the calorimeter was found to increase from $298.0 \ K$ to $298.45 \ K$ due to the combustion process. Given that the heat capacity of the calorimeter is $2.5 \ kJ \ K^{-1}$,the numerical value for the enthalpy of combustion of the gas in $kJ \ mol^{-1}$ is

An ideal gas expanded irreversibly against $10 \ bar$ pressure from $20 \ L$ to $30 \ L$. Calculate $Q$ if the process is isoenthalpic. $(1 \ L \ bar = 100 \ J)$

The enthalpy change on freezing of $1 \ mol$ of water at $5 \ ^\circ C$ to ice at $-5 \ ^\circ C$ is ..... $kJ \ mol^{-1}$.
(Given $\Delta _{fus}H = 6 \ kJ \ mol^{-1}$ at $0 \ ^\circ C$,
$C_p(H_2O, l) = 75.3 \ J \ mol^{-1} \ K^{-1}$,
$C_p(H_2O, s) = 36.8 \ J \ mol^{-1} \ K^{-1}$)

Calculate $\Delta S_{total}$ for the following reaction at $300 \ K$.
$NH_4NO_{3(s)} \longrightarrow NH_4^+{(aq)} + NO_3^-{(aq)}$ $(\Delta H = 28.1 \ kJ \ mol^{-1}, \Delta S_{sys} = 108.7 \ J \ K^{-1} \ mol^{-1})$

Enthalpy of formation of $CO_{2(g)}$,$H_2O_{(l)}$ and $C_6H_{12}O_{6(s)}$ are $-393$,$-286$ and $-1170 \ kJ \ mol^{-1}$ respectively. The quantity of heat liberated when $18 \ g$ of $C_6H_{12}O_{6(s)}$ is burnt completely in oxygen is (in $kJ$)