One mole of an ideal gas at $900 \ K$ undergoes two reversible processes,$I$ followed by $II$,as shown in the graph. If the work done by the gas in the two processes is the same,the value of $\ln \frac{V_3}{V_2}$ is. . . . . . . . ($U$: internal energy,$S$: entropy,$p$: pressure,$V$: volume,$R$: gas constant). (Given: molar heat capacity at constant volume,$C_{V, m}$ of the gas is $\frac{5}{2} R$)

  • A
    $2$
  • B
    $5$
  • C
    $8$
  • D
    $10$

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For the reaction at $25^{\circ} C$, $X_2O_{4(l)} \longrightarrow 2 XO_{2(g)}$, $\Delta U$ and $\Delta S$ are $2.1 \ kCal$ and $20 \ cal \ K^{-1}$ respectively. What is $\Delta G$ for the reaction at the same temperature? $(R = 2 \ cal \ K^{-1} \ mol^{-1})$

Identify the correct statements from the following.
$I$. At $0 \ K$,the entropy of pure crystalline materials approaches zero.
$II$. Entropy for the process,$H_2O_{(l)} \longrightarrow H_2O_{(g)}$ decreases.
$III$. Gibbs' energy is a state function.

Consider the reaction at $300 \ K$:
$C_6H_{6(l)} + \frac{15}{2}O_{2(g)} \longrightarrow 6CO_{2(g)} + 3H_2O_{(l)} ; \Delta H = -3271 \ kJ$
What is $\Delta U$ for the combustion of $1.5 \ mol$ of benzene at $27 \ ^\circ C$? .....$kJ$

At $25^{\circ} \text{C}$,$1 \text{ mole}$ of butane is combusted to form $CO_2$ and liquid $H_2O$. The work done is $...... \text{ L atm}$.

At $300 \ K$, $3.0 \ \text{moles}$ of an ideal gas at $3.0 \ \text{atm}$ pressure is compressed isothermally to one half of its volume by an external pressure of $6.0 \ \text{atm}$. The work done (in $kJ$) is. Given, $R=0.082 \ \text{L atm K}^{-1} \text{mol}^{-1}$ $(1 \ \text{L atm} = 101.3 \ \text{J})$.

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