$A$ thermodynamic cycle in the pressure $(p)-$ volume $(V)$ plane is given below. $A B$ and $C D$ are isothermal processes while $B C$ and $D A$ are adiabatic processes. The same cycle in the temperature $(T) -$ entropy $(S)$ plane is

Three moles of an ideal gas are expanded isothermally from a volume of $300 \ cm^3$ to $2.5 \ L$ at $300 \ K$ against a constant external pressure of $1.9 \ atm$. The work done in joules is:

The enthalpy change for the reaction of $50.00 \ mL$ of ethylene with $50.00 \ mL$ of $H_2$ at $1.5 \ atm$ pressure is $\Delta H = -0.31 \ kJ$. The value of $\Delta E$ will be (in $kJ$)

For a reaction $2 CO_{(g)} + O_{2(g)} \rightleftharpoons 2 CO_{2(g)}$,$\Delta_{r} G^0 = -128 \ kJ$ at $300 \ K$. If $\Delta_{r} S^0$ of the reaction is $-40 \ J \ K^{-1}$,calculate $\Delta_{r} U$ of the reaction. (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]

Calculate $\Delta H_f^o$ of $SiH_2$ from the following reactions:
$Si_2H_{6(g)} + H_{2(g)} \to 2SiH_{4(g)}, \Delta H = -11.7 \ kJ/mol$
$SiH_{4(g)} \to SiH_{2(g)} + H_{2(g)}, \Delta H = +239.7 \ kJ/mol$
$\Delta H_f^o(Si_2H_{6(g)}) = 80.3 \ kJ/mol$