The molar heat capacity $(C_p)$ of $CD_2O$ is $10 \, cal \, K^{-1} \, mol^{-1}$ at $1000 \, K$. The change in entropy associated with cooling of $32 \, g$ of $CD_2O$ vapour from $1000 \, K$ to $100 \, K$ at constant pressure will be.....$cal \, deg^{-1}$ ($D = $ deuterium,atomic mass $= 2 \, u$)

  • A
    $23.03$
  • B
    $-23.03$
  • C
    $2.303$
  • D
    $-2.303$

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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 $27 \ ^oC$? $..... \ kJ$

Standard entropies for $H_2, Cl_2$ and $HCl$ are $60, 40$ and $60 \ J \ K^{-1} \ mol^{-1}$ respectively. For the reaction $H_2 + Cl_2 \rightleftharpoons 2HCl$,with $\Delta H = +30 \ kJ$,the temperature at which the reaction will be at equilibrium is $..... \ K$.

Match the thermodynamic processes given under Column $I$ with the expression given under Column $II$:
Column $I$ Column $II$
$A$. Freezing of water at $273 \ K$ and $1 \ atm$ $P$. $q=0$
$B$. Expansion of $1 \ mol$ of an ideal gas into a vacuum under isolated conditions $Q$. $w=0$
$C$. Mixing of equal volumes of two ideal gases at constant temperature and pressure in an isolated container $R$. $\Delta S_{sys} < 0$
$D$. Reversible heating of $H_{2(g)}$ at $1 \ atm$ from $300 \ K$ to $600 \ K$,followed by reversible cooling to $300 \ K$ at $1 \ atm$ $S$. $\Delta U=0$
  $T$. $\Delta G=0$

Calculate the enthalpy change when $50 \ mL$ of $0.01 \ M$ $Ca(OH)_2$ reacts with $25 \ mL$ of $0.01 \ M$ $HCl$. Given that $\Delta H^o_{\text{neutralisation}}$ of strong acid and strong base is $-57.1 \ kJ \ mol^{-1}$. [Assuming that $Ca(OH)_2$ is a strong base]

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$1 \, \text{mole}$ of $H_2SO_4$ is mixed with $2 \, \text{moles}$ of $NaOH$. The heat evolved will be

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