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For the reaction I(2)(g) hArr 2I(g), K(c...

For the reaction `I_(2)(g) hArr 2I(g)`, `K_(c) 37.6 xx 10^(-6)` at 1000K . If 1.0 mole of `I_(2)` is introduced into a 1.0 litre flask at 1000K, at equilibrium

A

`[I_(2)]gt gt [I]`

B

`[I_(2)] = [I]`

C

`[I_(2)] lt [I]`

D

Unpredictable

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The correct Answer is:
To solve the problem, we need to analyze the equilibrium of the reaction: \[ I_2(g) \rightleftharpoons 2I(g) \] Given: - \( K_c = 37.6 \times 10^{-6} \) at \( 1000 \, K \) - Initial amount of \( I_2 = 1.0 \, \text{mole} \) in a \( 1.0 \, \text{litre} \) flask ### Step 1: Write the expression for the equilibrium constant \( K_c \) The equilibrium constant expression for the reaction is given by: \[ K_c = \frac{[I]^2}{[I_2]} \] ### Step 2: Determine initial concentrations Since we have 1 mole of \( I_2 \) in a 1.0 litre flask, the initial concentration of \( I_2 \) is: \[ [I_2]_{initial} = \frac{1.0 \, \text{mole}}{1.0 \, \text{litre}} = 1.0 \, \text{M} \] The initial concentration of \( I \) is \( 0 \, \text{M} \) because no iodine atoms are present initially. ### Step 3: Set up the change in concentrations at equilibrium Let \( x \) be the amount of \( I_2 \) that dissociates at equilibrium. Therefore, at equilibrium, we have: - Concentration of \( I_2 \): \( [I_2] = 1.0 - x \) - Concentration of \( I \): \( [I] = 2x \) ### Step 4: Substitute into the equilibrium expression Substituting these values into the \( K_c \) expression gives: \[ K_c = \frac{(2x)^2}{(1.0 - x)} = \frac{4x^2}{1.0 - x} \] ### Step 5: Set up the equation with the given \( K_c \) Now we can set this equal to the given \( K_c \): \[ 37.6 \times 10^{-6} = \frac{4x^2}{1.0 - x} \] ### Step 6: Solve for \( x \) Assuming \( x \) is small compared to 1.0 (which is reasonable given the small value of \( K_c \)), we can simplify the equation: \[ 37.6 \times 10^{-6} \approx \frac{4x^2}{1.0} \] This simplifies to: \[ 4x^2 = 37.6 \times 10^{-6} \] \[ x^2 = \frac{37.6 \times 10^{-6}}{4} \] \[ x^2 = 9.4 \times 10^{-7} \] \[ x = \sqrt{9.4 \times 10^{-7}} \approx 9.7 \times 10^{-4} \] ### Step 7: Calculate equilibrium concentrations Now substituting \( x \) back to find the equilibrium concentrations: - \( [I_2] = 1.0 - x \approx 1.0 - 9.7 \times 10^{-4} \approx 0.999 \, \text{M} \) - \( [I] = 2x \approx 2 \times 9.7 \times 10^{-4} \approx 1.94 \times 10^{-3} \, \text{M} \) ### Conclusion At equilibrium, the concentrations are approximately: - \( [I_2] \approx 0.999 \, \text{M} \) - \( [I] \approx 1.94 \times 10^{-3} \, \text{M} \)

To solve the problem, we need to analyze the equilibrium of the reaction: \[ I_2(g) \rightleftharpoons 2I(g) \] Given: - \( K_c = 37.6 \times 10^{-6} \) at \( 1000 \, K \) - Initial amount of \( I_2 = 1.0 \, \text{mole} \) in a \( 1.0 \, \text{litre} \) flask ...
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