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For a first order homogeneous gaseous re...

For a first order homogeneous gaseous reaction
`Ato 2B+C`
if the total pressure after time t was `P_(1)` and after long time `(t to infty)` was `P_(infty)` then K in terms of `P_(t_(1))` `P_(infty)` t is

A

`K=(2.303)/(t)log((P_(infty))/(P_(infty)-P_(t)))`

B

`K=(2.303)/(t)log((2P_(infty))/(P_(infty-P_(t))))`

C

`K=(2.303)/(t)log((2P_(infty))/(3(P_(infty-P_(t)))))`

D

none of these

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To solve the problem, we need to derive the expression for the rate constant \( K \) in terms of the total pressure at time \( t \) (denoted as \( P_t \)) and the total pressure at equilibrium (denoted as \( P_{\infty} \)) for the reaction \( A \to 2B + C \). ### Step-by-Step Solution: 1. **Identify Initial Conditions**: - At \( t = 0 \), only reactant \( A \) is present. Let the initial pressure of \( A \) be \( P_A \) and the pressures of \( B \) and \( C \) be \( 0 \). - Therefore, \( P(0) = P_A \). 2. **Define Pressures at Time \( t \)**: - At time \( t \), let \( P_{A} \) decrease by \( P_d \) (the pressure of \( A \) that has reacted). - The pressure of \( B \) formed will be \( 2P_d \) (since 2 moles of \( B \) are formed for every mole of \( A \) that reacts), and the pressure of \( C \) formed will be \( P_d \). - The total pressure at time \( t \) can be expressed as: \[ P_t = (P_A - P_d) + 2P_d + P_d = P_A + 2P_d \] - Rearranging gives: \[ P_d = \frac{P_t - P_A}{2} \] 3. **Define Pressures at Equilibrium**: - At \( t \to \infty \), all of \( A \) will have reacted, so: - \( P_A = 0 \) - The total pressure will be: \[ P_{\infty} = 2P_d + P_d = 3P_d \] - Therefore, we can express \( P_d \) in terms of \( P_{\infty} \): \[ P_d = \frac{P_{\infty}}{3} \] 4. **Substituting \( P_d \) into the Expression for \( P_t \)**: - Substitute \( P_d \) back into the equation for \( P_t \): \[ P_t = P_A + 2\left(\frac{P_{\infty}}{3}\right) = P_A + \frac{2P_{\infty}}{3} \] - Rearranging gives: \[ P_A = P_t - \frac{2P_{\infty}}{3} \] 5. **Using the First Order Reaction Rate Expression**: - For a first-order reaction, the rate constant \( K \) can be expressed as: \[ Kt = \ln\left(\frac{P_A}{P_t - P_A}\right) \] - Substitute \( P_A \) into this equation: \[ Kt = \ln\left(\frac{P_t - \frac{2P_{\infty}}{3}}{P_t - \left(P_t - \frac{2P_{\infty}}{3}\right)}\right) = \ln\left(\frac{P_t - \frac{2P_{\infty}}{3}}{\frac{P_{\infty}}{3}}\right) \] 6. **Final Expression for \( K \)**: - Rearranging gives: \[ K = \frac{1}{t} \ln\left(\frac{3(P_t - \frac{2P_{\infty}}{3})}{P_{\infty}}\right) \] - This can be simplified to: \[ K = \frac{1}{t} \ln\left(\frac{3P_t - 2P_{\infty}}{P_{\infty}}\right) \] ### Final Answer: \[ K = \frac{1}{t} \ln\left(\frac{3P_t - 2P_{\infty}}{P_{\infty}}\right) \]

To solve the problem, we need to derive the expression for the rate constant \( K \) in terms of the total pressure at time \( t \) (denoted as \( P_t \)) and the total pressure at equilibrium (denoted as \( P_{\infty} \)) for the reaction \( A \to 2B + C \). ### Step-by-Step Solution: 1. **Identify Initial Conditions**: - At \( t = 0 \), only reactant \( A \) is present. Let the initial pressure of \( A \) be \( P_A \) and the pressures of \( B \) and \( C \) be \( 0 \). - Therefore, \( P(0) = P_A \). ...
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