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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Similar Questions

From the following data,the enthalpy of dilution of $KCl$ will be ............ $kJ$.
$KCl_{(s)} + 20H_2O \to KCl(20H_2O); \Delta H = + 15.90 \ kJ$
$KCl_{(s)} + 200H_2O \to KCl(200H_2O); \Delta H = + 18.58 \ kJ$

At the temperature $T$ $(K)$ for the reaction: $X_2O_{4(l)} \rightarrow 2XO_{2(g)}$,given $\Delta U = x \ kJ \ mol^{-1}$ and $\Delta S = y \ J \ K^{-1} \ mol^{-1}$. The Gibbs energy change for the reaction is: (Assume $X_2O_4$ and $XO_2$ are ideal gases)

For the reaction $A_{(g)} + 2B_{(g)} \to 2C_{(g)} + 3D_{(g)}$,the value of $\Delta E$ at $27\ ^oC$ is $19.0\ kcal$. The value of $\Delta H$ for the reaction would be.......$kcal$ $(R = 2.0\ cal\ K^{-1} mol^{-1})$

Arrange the following isothermal processes in order of the magnitude of the work $(w)$ involved between states $1$ and $2$.
$A$. Expansion in single stage $(w_A)$
$B$. Expansion in multi stages $(w_B)$
$C$. Compression in single stage $(w_C)$
$D$. Compression in multi stages $(w_D)$

Match the following processes with their corresponding entropy changes:
Process Entropy Change
$(a)$ Liquid to vapor conversion $(1)$ $\Delta S = 0$
$(b)$ Process not spontaneous at any temperature $(2)$ $\Delta S = (+)$
$(c)$ Reversible expansion of an ideal gas $(3)$ $\Delta S = (-)$

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