For the gas-phase equilibrium the uncatalyzed rate constants at are (forward…

CHEMISTRY · Multi-part · AP · Chemistry · Kinetics · Kinetics

Problem

For the gas-phase equilibrium SO2Cl2 (g)⇌SO2 (g)+Cl2 (g)\mathrm{SO_2Cl_2\,(g)} \rightleftharpoons \mathrm{SO_2\,(g)} + \mathrm{Cl_2\,(g)} the uncatalyzed rate constants at 350 K350\,\text{K} are kf=1.5×10−5 s−1k_f = 1.5 \times 10^{-5}\,\text{s}^{-1} (forward decomposition) kr=3.0×10−5 s−1k_r = 3.0 \times 10^{-5}\,\text{s}^{-1} (reverse recombination) A solid catalyst is introduced that increases *both* rate constants by the same factor of 4.04.0. Assume that each elementary step is first order in the species that decomposes or recombines and that the system initially contains only SO2Cl2\mathrm{SO_2Cl_2} at a pressure of 0.800 atm0.800\,\text{atm}. (a) Write an expression for the equilibrium constant KpK_p in terms of the given rate constants and calculate its numerical value at 350 K350\,\text{K} before the catalyst is added. (b) Determine the numerical value of KpK_p after the catalyst is added. Show your reasoning. (c) Derive an expression for the characteristic time τ\tau required for the system to reach 63%63\% of its final approach to equilibrium for a reversible first-order reaction of this type. Your expression should be in terms of kfk_f and krk_r. (d) Calculate the ratio τcatalyzed/τuncatalyzed\tau_{\text{catalyzed}}/\tau_{\text{uncatalyzed}} using the data provided, and interpret what this ratio implies about the time needed to reach equilibrium.

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