Related Formula
P = (nRT)/(V) and Kₚ = (PN₂O₄)² · PO₂(PN₂O₅)²$$P = \frac{nRT}{V} \quad \text{and} \quad K_p = \frac{(P_{\mathrm{N}_2\mathrm{O}_4})^2 \cdot P_{\mathrm{O}_2}}{(P_{\mathrm{N}_2\mathrm{O}_5})^2}$$
Core Logic
First, find the initial moles of N₂O₅$\mathrm{N}_2\mathrm{O}_5$ using its molar mass (108 g/mol$108\text{ g/mol}$):
n₀ = (37.8)/(108) = 0.35 moles$$n_0 = \frac{37.8}{108} = 0.35\text{ moles}$$
Using the ideal gas equation, compute the initial pressure (Pᵢ$P_i$):
Pᵢ = (0.35 × 0.082 × 500)/(1) = 14.35 bar$$P_i = \frac{0.35 \times 0.082 \times 500}{1} = 14.35\text{ bar}$$
Setting up the equilibrium partial pressures table:
arraylccccc & 2N₂O5(g) & leftharpoons & 2N₂O4(g) & + & O2(g) Initially: & 14.35 & & 0 & & 0 At equilibrium: & 14.35 - 2P & & 2P & & P array$$\begin{array}{lccccc}
& 2\mathrm{N}_2\mathrm{O}_{5(\mathrm{g})} & \rightleftharpoons & 2\mathrm{N}_2\mathrm{O}_{4(\mathrm{g})} & + & \mathrm{O}_{2(\mathrm{g})} \\
\text{Initially: } & 14.35 & & 0 & & 0 \\
\text{At equilibrium: } & 14.35 - 2P & & 2P & & P
\end{array}$$
The total pressure at equilibrium is given as:
Ptotal = (14.35 - 2P) + 2P + P = 14.35 + P = 18.65 bar$$P_{\text{total}} = (14.35 - 2P) + 2P + P = 14.35 + P = 18.65\text{ bar}$$
P = 18.65 - 14.35 = 4.3 bar$$P = 18.65 - 14.35 = 4.3\text{ bar}$$
Now, calculate the equilibrium partial pressures for each component:
Kₚ = ((8.6)² × 4.3)/((5.75)²) = (73.96 × 4.3)/(33.0625) ≈ 9.619$$K_p = \frac{(8.6)^2 \times 4.3}{(5.75)^2} = \frac{73.96 \times 4.3}{33.0625} \approx 9.619$$
Expressing the result in the requested format (x × 10⁻²$x \times 10^{-2}$):
Kₚ = 961.9 × 10⁻²$$K_p = 961.9 \times 10^{-2}$$
Rounding to the nearest integer yields 962.
Pattern Recognition
Always calculate the initial pressure first using the ideal gas law (PV=nRT$PV=nRT$). This provides a clear baseline for tracking equilibrium partial pressures.
Chapter Mix
Class 11 Chemistry: Equilibrium