Let the concentration of N2O at equilibrium be x.
The given reaction is:
\(2N_2(g) + O_2(g) ↔ 2N_2O(g)\)
Initial conc. \(0.482\ mol\) \(0.933 \ mol\) \(0\)
At equilibrium \((0.482 - x)\ mol\) \((1.933 - x)\ mol\) \(x\) \(mol\)
Therefore, at equilibrium, in the 10 L vessel:
\([N_2] = \frac {0.482 - x }{10},\)
\([O_2] = \frac {0.933 - \frac x2}{10} ,\)
\([N2O] = \frac {x}{10}\)
The value of equilibrium constant i.e., \(K_c= 2.0 × 10^{-37}\) is very small. Therefore, the amount of N2 and O2 reacted is also very small. Thus, x can be neglected from the expressions of molar concentrations of N2 and O2.
Then, \([N_2] = \frac {0.482}{10} = 0.0482\ mol L^{-1 }\)
and \([O_2] = \frac {0.933}{10}= 0.0933 \ mol L^{-1}\)
Now,
\(K_c = \frac {[N_2O(g)]^2}{[N_2(g)]^2 [O_2(g)] }\)
⇒ \(2.0×10^{-37} = \frac {(\frac {x}{10})^2}{(0.0482)^2 (0.0933) }\)
⇒ \(\frac {x^2}{100} = 2.0×10^{-37}×(0.0482)^2×(0.0933)\)
⇒ \(x^2 = 43.35×10^{- 40}\)
⇒ \(x = 6.6×10^{-20}\)
\([N_2O] = \frac {x}{10}\)
\([N_2O] =\) \(\frac {6.6 × 10^{- 20}}{10}\)
\([N_2O] = 6.6×10^{-21}\)
For the reaction A(g) $\rightleftharpoons$ 2B(g), the backward reaction rate constant is higher than the forward reaction rate constant by a factor of 2500, at 1000 K.
[Given: R = 0.0831 atm $mol^{–1} K^{–1}$]
$K_p$ for the reaction at 1000 K is:
The equilibrium constant for decomposition of $ H_2O $ (g) $ H_2O(g) \rightleftharpoons H_2(g) + \frac{1}{2} O_2(g) \quad (\Delta G^\circ = 92.34 \, \text{kJ mol}^{-1}) $ is $ 8.0 \times 10^{-3} $ at 2300 K and total pressure at equilibrium is 1 bar. Under this condition, the degree of dissociation ($ \alpha $) of water is _____ $\times 10^{-2}$ (nearest integer value). [Assume $ \alpha $ is negligible with respect to 1]
Consider the following gas phase dissociation, PCl$_5$(g) $\rightleftharpoons$ PCl$_3$(g) + Cl$_2$(g) with equilibrium constant K$_p$ at a particular temperature and at pressure P. The degree of dissociation ($\alpha$) for PCl$_5$(g) is
PCl$_5$(g) $\rightleftharpoons$ PCl$_3$(g) + Cl$_2$(g)
The equilibrium constant may be defined as the ratio between the product of the molar concentrations of the products to that of the product of the molar concentrations of the reactants with each concentration term raised to a power equal to the stoichiometric coefficient in the balanced chemical reaction.
The equilibrium constant at a given temperature is the ratio of the rate constant of forwarding and backward reactions.
Kequ = kf/kb = [C]c [D]d/[A]a [B]b = Kc
where Kc, indicates the equilibrium constant measured in moles per litre.
For reactions involving gases: The equilibrium constant formula, in terms of partial pressure will be:
Kequ = kf/kb = [[pC]c [pD]d]/[[pA]a [pB]b] = Kp
Where Kp indicates the equilibrium constant formula in terms of partial pressures.
Medium Kc/Kp values indicate optimum product formation.
The equilibrium constant is the ratio of the concentrations raised to the stoichiometric coefficients. Therefore, the unit of the equilibrium constant = [Mole L-1]△n.
where, ∆n = sum of stoichiometric coefficients of products – a sum of stoichiometric coefficients of reactants.