For the reaction $H_{2}O_{(l)} \rightleftharpoons H_{2}O_{(g)}$ at $373 \ K$ and $1 \ atm$ pressure:

Which of the following statements or relationships is not correct in thermodynamic changes?

The $\Delta H$ for vaporisation of a liquid is $20 \, kJ/mol$. Assuming ideal behaviour,the change in internal energy for the vaporisation of $1 \, mole$ of the liquid at $60^{\circ} C$ and $1 \, bar$ is close to $.... \, kJ/mol$

For a reaction,$X_{2(g)} + Y_{2(g)} \rightleftharpoons 2XY_{(g)}$. If $\Delta G_r^o = 20 \ kJ \ mol^{-1}$ and $\Delta S_r^o = -20 \ J \ K^{-1} \ mol^{-1}$ at $200 \ K$. Calculate $\Delta H_r^o$ at $400 \ K$ (Given $\Delta_r C_P = 20 \ J \ K^{-1} \ mol^{-1}$).

Calculate the heat produced in $kJ$ when $280 \ g$ of $CaO$ is completely converted to $CaCO_3$ by reaction with $CO_2$ at $27 \ ^{\circ}C$ and at constant volume :-
(Given) $\Delta H^o_f (CaCO_3, s) = -1207 \ kJ/mol$
$\Delta H^o_f (CaO, s) = -635 \ kJ/mol$
$\Delta H^o_f (CO_2, g) = -394 \ kJ/mol$ (in $kJ$)

$0.3 \ g$ of ethane undergoes combustion at $27^{\circ} C$ in a bomb calorimeter. The temperature of the calorimeter system (including the water) is found to rise by $0.5^{\circ} C$. The heat evolved during combustion of ethane at constant pressure is $....... kJ \ mol^{-1}$. (Nearest integer) [Given: The heat capacity of the calorimeter system is $20 \ kJ \ K^{-1}$,$R = 8.3 \ J \ K^{-1} \ mol^{-1}$. Assume ideal gas behaviour. Atomic mass of $C$ and $H$ are $12$ and $1 \ g \ mol^{-1}$ respectively]