At $67\,^{\circ}C$ and $1\ bar$ pressure,dinitrogen tetraoxide is $50\%$ dissociated into nitrogen dioxide. $\Delta G^{\circ}$ for the process $N_2O_{4(g)} \rightleftharpoons 2NO_{2(g)}$ is $(R = \frac{25}{3} \ J \ K^{-1} \ mol^{-1}, \ln 2 = 0.7, \ln 3 = 1.1)$.

  • A
    $- 850 \ J \ mol^{-1}$
  • B
    $+ 850 \ J \ mol^{-1}$
  • C
    $- 850 \ kJ \ mol^{-1}$
  • D
    $+ 850 \ kJ \ mol^{-1}$

Explore More

Similar Questions

The dissociation of $CO_2$ is represented as $2CO_2(g) \rightleftharpoons 2CO(g) + O_2(g)$. If $2 \ mol$ of $CO_2$ are taken initially and $40\%$ of $CO_2$ dissociates,what will be the total number of moles at equilibrium?

In a $1.0 \, L$ vessel at $90 \, ^\circ C$,$0.2 \, mol$ of $H_{2(g)}$ and $2.0 \, mol$ of $S_{(s)}$ are mixed. For the reaction $H_{2(g)} + S_{(s)} \rightleftharpoons H_2S_{(g)}$; $K_p = 6.8 \times 10^{-2}$,the partial pressure of $H_2S_{(g)}$ at equilibrium will be ............ $atm$.

$28 \, g$ of $N_2$ and $6 \, g$ of $H_2$ were kept at $400 \, ^oC$ in a $1 \, L$ vessel. The equilibrium mixture contained $27.54 \, g$ of $NH_3$. The approximate value of $K_c$ for the reaction $N_2(g) + 3H_2(g) \rightleftharpoons 2NH_3(g)$ is (in $L^2 \, mol^{-2}$):

For the reaction $N_{2(g)} + O_{2(g)} \rightleftharpoons 2NO_{(g)}$,the equilibrium constant is $K_1$. For the reaction $2NO_{(g)} + O_{2(g)} \rightleftharpoons 2NO_{2(g)}$,the equilibrium constant is $K_2$. The equilibrium constant $K$ for the reaction $NO_{2(g)} \rightleftharpoons \frac{1}{2}N_{2(g)} + O_{2(g)}$ will be:

Thermal decomposition of gaseous $X_2$ to gaseous $X$ at $298 \ K$ takes place according to the following equation :
$X_{2(g)} \rightleftharpoons 2 X_{(g)}$
The standard reaction Gibbs energy,$\Delta_r G^{\circ}$,of this reaction is positive. At the start of the reaction,there is one mole of $X_2$ and no $X$. As the reaction proceeds,the number of moles of $X$ formed is given by $\beta$. Thus,$\beta_{\text{equilibrium}}$ is the number of moles of $X$ formed at equilibrium. The reaction is carried out at a constant total pressure of $2 \ bar$. Consider the gases to behave ideally. (Given : $R=0.083 \ L \ bar \ K^{-1} \ mol^{-1}$)
$(1)$ The equilibrium constant $K_P$ for this reaction at $298 \ K$,in terms of $\beta_{\text{equilibrium}}$,is
$(A)$ $\frac{8 \beta_{\text{equilibrium}}^2}{2-\beta_{\text{equilibrium}}}$ $(B)$ $\frac{8 \beta_{\text{equilibrium}}^2}{4-\beta_{\text{equilibrium}}^2}$ $(C)$ $\frac{4 \beta_{\text{equilibrium}}^2}{2-\beta_{\text{equilibrium}}}$ $(D)$ $\frac{4 \beta_{\text{equilibrium}}^2}{4-\beta_{\text{equilibrium}}^2}$
$(2)$ The $INCORRECT$ statement among the following,for this reaction,is
$(A)$ Decrease in the total pressure will result in formation of more moles of gaseous $X$
$(B)$ At the start of the reaction,dissociation of gaseous $X_2$ takes place spontaneously
$(C)$ $\beta_{\text{equilibrium}}=0.7$
$(D)$ $K_c < 1$

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo