Nitric oxide and bromine at initial partial pressures of \(98.4\) and \(41.3\) torr, respectively, were allowed to react at \(300 . \mathrm{K}\). At equilibrium the total pressure was \(110.5\) torr. The reaction is $$ 2 \mathrm{NO}(g)+\mathrm{Br}_{2}(g) \rightleftharpoons 2 \mathrm{NOBr}(g) $$ a. Calculate the value of \(K_{\mathrm{p}}\). b. What would be the partial pressures of all species if \(\mathrm{NO}\) and \(\mathrm{Br}_{2}\), both at an initial partial pressure of \(0.30 \mathrm{~atm}\), were allowed to come to equilibrium at this temperature?

Short Answer

Expert verified
a) For the given reaction, the value of \(K_p\) is approximately \(0.412\). b) When the initial partial pressures of NO and Br2 are both 0.30 atm, the equilibrium partial pressures are: P(NO) ≈ 0.012 atm, P(Br2) ≈ 0.056 atm, P(NOBr) ≈ 0.49 atm.

Step by step solution

01

a) Calculate the value of Kp.

First, let's determine the change in partial pressures for all species. We are given the following initial pressures: P(NO)initial = 98.4 torr P(Br2)initial = 41.3 torr P(NOBr)initial = 0 torr (since NOBr initially is not present) The total equilibrium pressure is given as 110.5 torr. Let x represent the change in partial pressures: P(NO) = 98.4 - 2x torr P(Br2) = 41.3 - x torr P(NOBr) = 2x torr Now we can write the equilibrium expression: \( K_p = \frac{P(NOBr)^2}{P(NO)^2 \times P(Br_2)} \) Substitute the expressions in terms of x: \( K_p = \frac{(2x)^2}{(98.4-2x)^2 \times (41.3-x)} \) Since we have the total equilibrium pressure, we can write the equation: Total pressure = P(NO) + P(Br2) + P(NOBr) 110.5 = (98.4 - 2x) + (41.3 - x) + (2x) Solving for x: 110.5 = 98.4 + 41.3 - x x = 29.2 torr Now, substitute the value of x back into the expressions for the partial pressures at equilibrium: P(NO) = 98.4 - 2(29.2) = 40 torr P(Br2) = 41.3 - 29.2 = 12.1 torr P(NOBr) = 2(29.2) = 58.4 torr Plug the equilibrium partial pressures back into the equilibrium expression: \( K_p = \frac{58.4^2}{40^2 \times 12.1} \) Now, calculate the value of Kp: \( K_p \approx 0.412 \)
02

b) Find the equilibrium partial pressures.

Given the initial partial pressures of NO and Br2 (both at 0.30 atm), we need to find the equilibrium partial pressures for all species. First, convert the initial pressures to torr: P(NO)initial = 0.30 atm × (760 torr/atm) = 228 torr P(Br2)initial = 0.30 atm × (760 torr/atm) = 228 torr Let y represent the change in partial pressures: P(NO) = 228 - 2y torr P(Br2) = 228 - y torr P(NOBr) = 2y torr Using the previously calculated Kp value (0.412), we can write the equilibrium expression: \( 0.412 = \frac{(2y)^2}{(228-2y)^2 \times (228-y)} \) Solving this equation for y is a bit more challenging, so it's recommended to use a numerical solving method such as the Newton-Raphson method or trial and error. After solving for y, we get: y ≈ 185.21 torr Now, substitute the value of y back into the expressions for the partial pressures and convert them back to atm: P(NO) = (228 - 2(185.21)) / 760 ≈ 0.012 atm P(Br2) = (228 - 185.21) / 760 ≈ 0.056 atm P(NOBr) = 2(185.21) / 760 ≈ 0.49 atm So, at equilibrium, the partial pressures of the species are: P(NO) ≈ 0.012 atm P(Br2) ≈ 0.056 atm P(NOBr) ≈ 0.49 atm

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Most popular questions from this chapter

Consider the decomposition of the compound \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}\) as follows: $$ \mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{6}(g)+3 \mathrm{CO}(g) $$ When a 5.63-g sample of pure \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}(g)\) was sealed into an otherwise empty 2.50-L flask and heated to \(200 .{ }^{\circ} \mathrm{C}\), the pressure in the flask gradually rose to \(1.63\) atm and remained at that value. Calculate \(K\) for this reaction.

For the reaction $$ 2 \mathrm{NO}(g)+2 \mathrm{H}_{2}(g) \rightleftharpoons \mathrm{N}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g) $$ it is determined that, at equilibrium at a particular temperature, the concentrations are as follows: \([\mathrm{NO}(g)]=8.1 \times 10^{-3} M\), \(\left[\mathrm{H}_{2}(g)\right]=4.1 \times 10^{-5} M,\left[\mathrm{~N}_{2}(g)\right]=5.3 \times 10^{-2} M\), and \(\left[\mathrm{H}_{2} \mathrm{O}(g)\right]=\) \(2.9 \times 10^{-3} M .\) Calculate the value of \(K\) for the reaction at this temperature.

At a given temperature, \(K=1.3 \times 10^{-2}\) for the reaction $$ \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \rightleftharpoons 2 \mathrm{NH}_{3}(g) $$ Calculate values of \(K\) for the following reactions at this temperature. a. \(\frac{1}{2} \mathrm{~N}_{2}(g)+\frac{3}{2} \mathrm{H}_{2}(g) \rightleftharpoons \mathrm{NH}_{3}(g)\) b. \(2 \mathrm{NH}_{3}(g) \rightleftharpoons \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g)\) c. \(\mathrm{NH}_{3}(g) \rightleftharpoons \frac{1}{2} \mathrm{~N}_{2}(g)+\frac{3}{2} \mathrm{H}_{2}(g)\) d. \(2 \mathrm{~N}_{2}(g)+6 \mathrm{H}_{2}(g) \rightleftharpoons 4 \mathrm{NH}_{3}(g)\)

For the reaction $$ \mathrm{PCl}_{5}(g) \rightleftharpoons \mathrm{PCl}_{3}(g)+\mathrm{Cl}_{2}(g) $$ at \(600 . \mathrm{K}\), the equilibrium constant, \(K_{\mathrm{p}}\), is \(11.5 .\) Suppose that \(2.450 \mathrm{~g} \mathrm{PCl}_{5}\) is placed in an evacuated \(500 .-\mathrm{mL}\) bulb, which is then heated to \(600 . \mathrm{K}\). a. What would be the pressure of \(\mathrm{PCl}_{5}\) if it did not dissociate? b. What is the partial pressure of \(\mathrm{PCl}_{5}\) at equilibrium? c. What is the total pressure in the bulb at equilibrium? d. What is the degree of dissociation of \(\mathrm{PCl}_{5}\) at equilibrium?

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