A 1.0-L reaction vessel at \(90^{\circ} \mathrm{C}\) contains \(8.00 \mathrm{~g}\) of sulfur, hydrogen, and hydrogen sulfide gases with partial pressures of \(6.0 \mathrm{~atm}\) and \(0.40 \mathrm{~atm}\), respectively, at equilibrium: $$\mathrm{H}_{2}(g)+\mathrm{S}(s) \rightleftharpoons \mathrm{H}_{2} \mathrm{~S}(g)$$ (a) Calculate \(K\) for the reaction at equilibrium. (b) The mass of sulfur is increased to \(10.0\) grams. What are the partial pressures of \(\mathrm{H}_{2}\) and \(\mathrm{H}_{2} \mathrm{~S}\) when equilibrium is reestablished? (c) The pressure of \(\mathrm{H}_{2} \mathrm{~S}\) is increased to \(1.0 \mathrm{~atm}\). What are the partial pressures of \(\mathrm{H}_{2}\) and \(\mathrm{H}_{2} \mathrm{~S}\) when equilibrium is reestablished?

Short Answer

Expert verified
Question: Calculate the equilibrium constant K based on the given equilibrium partial pressures of hydrogen gas (H_2) and hydrogen sulfide (H_2S). Answer: The equilibrium constant K is 0.0667.

Step by step solution

01

(Part a - Calculating the equilibrium constant K)

Given the initial partial pressures of hydrogen gas (H_2) and hydrogen sulfide (H_2S) at equilibrium, we are asked to calculate the equilibrium constant K for the given reaction. First, we need to write an equilibrium expression involving the partial pressures: $$K_p = \frac{P_{H_2S}}{P_{H_2}}$$ Now, we can use the given values to find the equilibrium constant K: $$K_p = \frac{0.40\,\mathrm{atm}}{6.0\,\mathrm{atm}} = 0.0667$$
02

(Part b - Finding the partial pressures with increased sulfur mass)

We are given that the mass of sulfur is increased from 8.00 g to 10.00 g. Since H_2S is formed from both H_2 and S, the additional S will push the reaction towards the formation of H_2S. Let (x) be the increase in the partial pressure of H_2S at the new equilibrium. Applying stoichiometry and using the initial values: $$P_{H_2S, new} = 0.40\,\mathrm{atm} + x$$ $$P_{H_2, new} = 6.0\,\mathrm{atm} - x$$ Next, we can write a new equilibrium expression using these values: $$K_p = \frac{P_{H_2S, new}}{P_{H_2, new}} = \frac{0.40 + x}{6.0 - x} = 0.0667$$ Now, solve for x: $$x = 0.363\,\mathrm{atm}$$ Substituting x back into our expressions for the new partial pressures, we get: $$P_{H_2S, new} = 0.763\,\mathrm{atm}$$ $$P_{H_2, new} = 5.637\,\mathrm{atm}$$ These are the new equilibrium partial pressures of H_2 and H_2S after increasing the mass of sulfur.
03

(Part c - Finding the partial pressures with increased H_2S pressure)

We are given that the pressure of H_2S is increased to 1.0 atm. Increasing the pressure of H_2S will push the reaction towards the formation of H_2 and S. Let (y) be the increase in partial pressure of H_2 at the new equilibrium. Applying stoichiometry and using the initial values: $$P_{H_2S, new} = 1.0\,\mathrm{atm} - y$$ $$P_{H_2, new} = 6.0\,\mathrm{atm} + y$$ Write an equilibrium expression with these new values: $$K_p = \frac{P_{H_2S, new}}{P_{H_2, new}} = \frac{1.0 - y}{6.0 + y} = 0.0667$$ Now, solve for y: $$y = -0.2\,\mathrm{atm}$$ Note that a negative value for y is not physically meaningful because we originally increased the pressure of H_2S. This means that adding H_2S has not affected the equilibrium, and the partial pressures of H_2 and H_2S remain unchanged. Therefore, the partial pressures of H_2 and H_2S when equilibrium is reestablished are the same as initially given: $$P_{H_2} = 6.0\,\mathrm{atm}$$ $$P_{H_2S} = 0.40\,\mathrm{atm}$$

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Most popular questions from this chapter

At a certain temperature, \(K\) is \(1.3 \times 10^{5}\) for the reaction $$2 \mathrm{H}_{2}(g)+\mathrm{S}_{2}(g) \rightleftharpoons 2 \mathrm{H}_{2} \mathrm{~S}(g)$$ What is the equilibrium pressure of hydrogen sulfide if those of hydrogen and sulfur gases are \(0.103\) atm and \(0.417\) atm, respectively?

Given the following reactions and their equilibrium constants, $$\begin{array}{cl}\mathrm{C}(s)+\mathrm{CO}_{2}(g) \rightleftharpoons 2 \mathrm{CO}(g) & K=2.4 \times 10^{-9} \\ \mathrm{COCl}_{2}(g) \rightleftharpoons \mathrm{CO}(g)+\mathrm{Cl}_{2}(g) & K=8.8 \times 10^{-13} \end{array}$$ calculate \(K\) for the reaction $$\mathrm{C}(s)+\mathrm{CO}_{2}(g)+2 \mathrm{Cl}_{2}(g) \rightleftharpoons 2 \mathrm{COCl}_{2}(g)$$

The following data are for the system $$\mathrm{A}(g) \rightleftharpoons 2 \mathrm{~B}(g)$$ $$\begin{array}{ccccccc}\hline \text { Time (s) } & 0 & 30 & 45 & 60 & 75 & 90 \\\ P_{\mathrm{A}} \text { (atm) } & 0.500 & 0.390 & 0.360 & 0.340 & 0.325 & 0.325 \\\ P_{\text {B }} \text { (atm) } & 0.000 & 0.220 & 0.280 & 0.320 & 0.350 & 0.350 \\\\\hline\end{array}$$ (a) How long does it take the system to reach equilibrium? (b) How does the rate of the forward reaction compare with the rate of the reverse reaction after 45 s? After 90 s?

The reversible reaction between hydrogen chloride gas and one mole of oxygen gas produces steam and chlorine gas: $$4 \mathrm{HCl}(g)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{Cl}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g) \quad K=0.79$$ Predict the direction in which the system will move to reach equilibrium if one starts with (a) \(P_{\mathrm{H}_{2} \mathrm{O}}=P_{\mathrm{HCl}}=P_{\mathrm{O}_{2}}=0.20 \mathrm{~atm}\) (b) \(P_{\mathrm{HCl}}=0.30 \mathrm{~atm}, P_{\mathrm{H}_{2} \mathrm{O}}=0.35 \mathrm{~atm}, P_{\mathrm{Cl}_{2}}=0.2 \mathrm{~atm}, P_{\mathrm{O}_{2}}=0.15 \mathrm{~atm}\)

For the system $$\mathrm{SO}_{3}(g) \rightleftharpoons \mathrm{SO}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g)$$ at \(1000 \mathrm{~K}, K=0.45 .\) Sulfur trioxide, originally at \(1.00 \mathrm{~atm}\) pressure, partially dissociates to \(\mathrm{SO}_{2}\) and \(\mathrm{O}_{2}\) at \(1000 \mathrm{~K}\). What is its partial pressure at equilibrium?

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