Given:
Step 1: Establish the Change in Moles
Let \( x \) be the moles of \(\mathrm{N_2}\) that react. According to the stoichiometry: \[ \begin{array}{lcc} & \mathrm{N_2} & + 3\mathrm{H_2} \rightleftharpoons 2\mathrm{NH_3} \\ \text{Initial (moles):} & 1 & 3 \quad 0 \\ \text{Change (moles):} & -x & -3x \quad +2x \\ \text{Equilibrium (moles):} & 1-x & 3-3x \quad 2x \\ \end{array} \]
Step 2: Solve for \( x \)
Given that at equilibrium, 0.4 moles of \(\mathrm{NH_3}\) are present: \[ 2x = 0.4 \implies x = 0.2 \text{ moles} \]
Step 3: Calculate Equilibrium Moles of \(\mathrm{H_2}\)
Substitute \( x = 0.2 \) into the equilibrium expression for \(\mathrm{H_2}\): \[ \text{Moles of } \mathrm{H_2} = 3 - 3x = 3 - 3(0.2) = 3 - 0.6 = 2.4 \text{ moles} \]
Step 4: Verification
Conclusion
The equilibrium concentration of \(\mathrm{H_2}\) is \(\boxed{2.4 \text{ moles}}\).
Final Answer
Based on standard equilibrium calculations, the correct equilibrium concentration of \(\mathrm{H_2}\) is: \[ \boxed{2.4 \text{ moles}} \]
The solubility of barium iodate in an aqueous solution prepared by mixing 200 mL of 0.010 M barium nitrate with 100 mL of 0.10 M sodium iodate is $X \times 10^{-6} \, \text{mol dm}^{-3}$. The value of $X$ is ------.
Use: Solubility product constant $(K_{sp})$ of barium iodate = $1.58 \times 10^{-9}$
For the reaction \( \text{N}_2(g) + 3\text{H}_2(g) \rightleftharpoons 2\text{NH}_3(g) \) at 298 K, the enthalpy change \( \Delta H = -92.4 \, \text{kJ/mol} \). What happens to the equilibrium when temperature is increased?
At 700 K, the equilibrium constant $K_e$ for the reaction $ \text{N}_2(g) + 3\text{H}_2(g) \rightleftharpoons 2\text{NH}_3(g) $ is 0.2 mol L$^{-2}$. What is the value of $K$ for the reverse reaction?
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: