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 $.... \, kJ/mol$

In the reaction at $300 \ K$:
$C_6H_6(\ell) + \frac{15}{2}O_{2(g)} \to 6CO_{2(g)} + 3H_2O(\ell) \quad \Delta H = -3271 \ kJ$
What is the value of $\Delta U$ for the combustion of $1.5 \ mol$ of benzene at $27 \ ^oC$? $..... \ kJ$

$11.0 \ L$ of an ideal gas at a constant external pressure of $5 \ atm$ is compressed isothermally to a final volume of $1 \ L$. The heat absorbed and work done,respectively,during this compression (in $L \ atm$) are:

$A$ mixture of $H_2$ and a sufficient quantity of air at $25\,^{\circ}C$ and $1\ atm$ pressure undergoes complete combustion in a closed rigid adiabatic container,leaving behind $H_2O_{(g)}$ and $N_{2(g)}$. If air is a mixture of $80\% N_2$ and $20\% O_2$ by volume and $C_{P(N_2)}$ and $C_{P(H_2O)g}$ are $7.0$ and $8.0\ cal\ deg^{-1}\ mol^{-1}$ respectively,what will be the maximum temperature attained? (Given that: $(\Delta H^o_f)_{H_2O_{(g)}} = -56.0\ kcal/mol$ and it is independent of temperature)...... $K$

In a reversible process,under what condition does the heat exchanged become a state function?

The energy of combustion per mole of $H_2$,$LPG$,and octane follows the order: