The equilibrium constant \(K_{\mathrm{p}}\) for the reaction $$\mathrm{CCl}_{4}(g) \rightleftharpoons \mathrm{C}(s)+2 \mathrm{Cl}_{2}(g)$$ at \(700^{\circ} \mathrm{C}\) is \(0.76 .\) Determine the initial pressure of carbon tetrachloride that will produce a total equilibrium pressure of 1.20 \(\mathrm{atm}\) at \(700^{\circ} \mathrm{C} .\)

Short Answer

Expert verified
The initial pressure of carbon tetrachloride that will produce a total equilibrium pressure of 1.20 atm at 700°C is approximately 0.9696 atm.

Step by step solution

01

Initial and Equilibrium Pressures

Let x be the moles of CCl₄ that reacted at equilibrium. The initial pressure of CCl₄ is P(CCl₄) and since there was no Cl₂ in the beginning, we can write the pressures at equilibrium as: P(CCl₄) - x for CCl₄ 2x for Cl₂ Note that, since Carbon in the reaction is in solid state, it doesn't affect the pressures. The total equilibrium pressure is given as 1.20 atm. So, (P(CCl₄) - x) + 2x = 1.20 Simplifying the equation, we get: P(CCl₄) + x = 1.20
02

Write the expression for Kp

We are given the equilibrium constant Kp = 0.76. The expression for Kp, using the pressures of gases at equilibrium, is: Kp = \(\dfrac{(P(Cl_2))^2}{P(CCl_4)}\) At equilibrium, the pressure of Cl₂ is 2x. Thus, we can rewrite the expression as: 0.76 = \(\dfrac{(2x)^2}{P(CCl_4) - x}\)
03

Solving for the initial pressure of CCl₄

Now, we can rewrite our Kp equation in terms of x and P(CCl₄) only: 0.76 = \(\dfrac{4x^2}{P(CCl_4) - x}\) Using the equation from Step 1 (P(CCl₄) + x = 1.20), we can eliminate P(CCl₄) and solve for x: P(CCl₄) - x = 1.20 - 2x Now, we can substitute this expression in our Kp equation: 0.76 = \(\dfrac{4x^2}{1.20 - 2x}\) Let's isolate x in the equation: 0.76(1.20 - 2x) = 4x² After simplifying the equation, we get: 0.912 - 1.52x = 4x² Rearranging terms, we obtain the quadratic equation: 4x² + 1.52x - 0.912 = 0 We can solve this quadratic equation for x using any method (e.g., quadratic formula, factoring, etc.). Here, we will use the quadratic formula: x = \(\dfrac{-b \pm \sqrt{b^2 - 4ac}}{2a}\) where a = 4, b = 1.52, and c = -0.912. Calculating x, we get two possible values: x₁ ≈ 0.2304 and x₂ ≈ -0.991. Since x represents moles reacting and cannot be negative, we discard x₂ and use x₁: x ≈ 0.2304
04

Calculate the initial pressure of CCl₄

Now that we have the value of x, we can find the initial pressure of CCl₄ using the equation from Step 1: P(CCl₄) + x = 1.20 P(CCl₄) + 0.2304 = 1.20 P(CCl₄) ≈ 1.20 - 0.2304 P(CCl₄) ≈ 0.9696 atm The initial pressure of carbon tetrachloride that will produce a total equilibrium pressure of 1.20 atm at 700°C is approximately 0.9696 atm.

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Most popular questions from this chapter

For the reaction: $$3 \mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{O}_{3}(g)$$ \(K=1.8 \times 10^{-7}\) at a certain temperature. If at equilibrium \(\left[\mathrm{O}_{2}\right]=0.062 M,\) calculate the equilibrium \(\mathrm{O}_{3}\) concentration.

Write the equilibrium expression (K) for each of the following gas-phase reactions. a. \(N_{2}(g)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{NO}(g)\) b. \(\mathrm{N}_{2} \mathrm{O}_{4}(g) \rightleftharpoons 2 \mathrm{NO}_{2}(g)\) c. $\operatorname{SiH}_{4}(g)+2 \mathrm{Cl}_{2}(g) \rightleftharpoons \operatorname{SiCl}_{4}(g)+2 \mathrm{H}_{2}(g)$ d. $2 \mathrm{PBr}_{3}(g)+3 \mathrm{Cl}_{2}(g) \rightleftharpoons 2 \mathrm{PCl}_{3}(g)+3 \mathrm{Br}_{2}(g)$

A 4.72 -g sample of methanol (CH_ 3 \(\mathrm{OH}\) ) was placed in an otherwise empty \(1.00-\mathrm{L}\) flask and heated to \(250 .^{\circ} \mathrm{C}\) to vaporize the methanol. Over time, the methanol vapor decomposed by the following reaction: $$\mathrm{CH}_{3} \mathrm{OH}(g) \rightleftharpoons \mathrm{CO}(g)+2 \mathrm{H}_{2}(g)$$ After the system has reached equilibrium, a tiny hole is drilled in the side of the flask allowing gaseous compounds to effuse out of the flask. Measurements of the effusing gas show that it contains 33.0 times as much \(\mathrm{H}_{2}(g)\) as \(\mathrm{CH}_{3} \mathrm{OH}(g) .\) Calculate \(K\) for this reaction at \(250 . \mathrm{C} .\)

At a particular temperature, 12.0 moles of \(\mathrm{SO}_{3}\) is placed into a 3.0 -L rigid container, and the \(\mathrm{SO}_{3}\) dissociates by the reaction $$2 \mathrm{SO}_{3}(g) \rightleftharpoons 2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g)$$At equilibrium, 3.0 moles of \(\mathrm{SO}_{2}\) is present. Calculate \(K\) for this reaction.

Calculate a value for the equilibrium constant for the reaction $$\mathrm{O}_{2}(g)+\mathrm{O}(g) \rightleftharpoons \mathrm{O}_{3}(g)$$ given $$\mathrm{NO}_{2}(g) \stackrel{h \nu}{\rightleftharpoons} \mathrm{NO}(g)+\mathrm{O}(g) \quad K=6.8 \times 10^{-49}$$ $$\mathrm{O}_{3}(g)+\mathrm{NO}(g) \rightleftharpoons \mathrm{NO}_{2}(g)+\mathrm{O}_{2}(g) \quad K=5.8 \times 10^{-34}$$ (Hint: When reactions are added together, the equilibrium expressions are multiplied.)

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