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1 mole of 'A' 1.5 mole of 'B' and 2 mole...

1 mole of 'A' 1.5 mole of 'B' and 2 mole of 'C' are taken in a vessel of volume one litre. At equilibrium concentration of C is 0.5 mole /L .Equilibrium constant for the reaction , `A_((g))+B_((g) hArr C_((g))` is

A

0.66

B

0.066

C

66

D

6.6

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To solve the problem, we need to find the equilibrium constant \( K_c \) for the reaction: \[ A_{(g)} + B_{(g)} \rightleftharpoons C_{(g)} \] ### Step-by-Step Solution: 1. **Identify Initial Moles and Concentrations**: - Initial moles of \( A = 1 \) mole - Initial moles of \( B = 1.5 \) moles - Initial moles of \( C = 2 \) moles - Volume of the vessel = 1 L - Therefore, initial concentrations: \[ [A]_{initial} = 1 \, \text{mol/L}, \quad [B]_{initial} = 1.5 \, \text{mol/L}, \quad [C]_{initial} = 2 \, \text{mol/L} \] 2. **Determine the Change in Concentration**: - At equilibrium, the concentration of \( C \) is given as \( 0.5 \, \text{mol/L} \). - The initial concentration of \( C \) was \( 2 \, \text{mol/L} \). - Change in concentration of \( C \): \[ \Delta[C] = 2 - 0.5 = 1.5 \, \text{mol/L} \] 3. **Establish Changes for \( A \) and \( B \)**: - Since the reaction produces \( C \) from \( A \) and \( B \), the change in concentrations for \( A \) and \( B \) will be equal to the change in \( C \): \[ \Delta[A] = -1.5 \, \text{mol/L}, \quad \Delta[B] = -1.5 \, \text{mol/L} \] 4. **Calculate Equilibrium Concentrations**: - Equilibrium concentration of \( A \): \[ [A]_{equilibrium} = [A]_{initial} + \Delta[A] = 1 - 1.5 = -0.5 \, \text{mol/L} \, (\text{not possible, hence check the approach}) \] - Since \( C \) decreased by \( 1.5 \, \text{mol/L} \), we need to consider that \( C \) is actually increasing from the reverse reaction: \[ [C]_{equilibrium} = 2 + x \quad \text{where } x = 1.5 \text{ (the amount that reacted)} \] - Thus, \( [C]_{equilibrium} = 0.5 \) is consistent with the decrease in \( C \) from \( 2 \). 5. **Recalculate \( x \)**: - Let \( x \) be the amount of \( C \) that dissociated: \[ [C]_{equilibrium} = 2 - x = 0.5 \implies x = 1.5 \] - Therefore, at equilibrium: \[ [A]_{equilibrium} = 1 - x = 1 - 1.5 = -0.5 \, \text{(not valid)} \] - This indicates that the reaction has shifted to the left, and we need to adjust our calculations. 6. **Final Equilibrium Concentrations**: - \( [A]_{equilibrium} = 1 + 1.5 = 2.5 \, \text{mol/L} \) - \( [B]_{equilibrium} = 1.5 + 1.5 = 3 \, \text{mol/L} \) - \( [C]_{equilibrium} = 0.5 \, \text{mol/L} \) 7. **Calculate the Equilibrium Constant \( K_c \)**: - The expression for \( K_c \) is: \[ K_c = \frac{[C]_{equilibrium}}{[A]_{equilibrium} \cdot [B]_{equilibrium}} = \frac{0.5}{(2.5)(3)} \] - Calculate \( K_c \): \[ K_c = \frac{0.5}{7.5} = \frac{1}{15} \approx 0.0667 \] ### Final Answer: The equilibrium constant \( K_c \) for the reaction is approximately \( 0.0667 \).
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