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Given \(K=3.50\) at \(45^{\circ} \mathrm{C}\) for the reaction $$\mathrm{A}(g)+\mathrm{B}(g) \rightleftharpoons \mathrm{C}(g)$$ and \(K=7.10\) at \(45^{\circ} \mathrm{C}\) for the reaction $$2 \mathrm{A}(g)+\mathrm{D}(g) \rightleftharpoons \mathrm{C}(g)$$ what is the value of \(K\) at the same temperature for the reaction $$\mathrm{C}(g)+\mathrm{D}(g) \rightleftharpoons 2 \mathrm{B}(g)$$ What is the value of \(K_{\mathrm{p}}\) at \(45^{\circ} \mathrm{C}\) for the reaction? Starting with 1.50 atm partial pressures of both \(\mathrm{C}\) and \(\mathrm{D},\) what is the mole fraction of \(\mathrm{B}\) once equilibrium is reached?

Short Answer

Expert verified
The value of \(K_3\) at the same temperature for the reaction \(C(g) + D(g) \rightleftharpoons 2B(g)\) is 1.725. The mole fraction of B once equilibrium is reached is approximately 0.312.

Step by step solution

01

Write down all given information

We are given the following information: 1. For the reaction: \(A(g) + B(g) \rightleftharpoons C(g)\), we have \(K_1 = 3.50\) at \(45^\circ \mathrm{C}\) 2. For the reaction: \(2A(g) + D(g) \rightleftharpoons C(g)\), we have \(K_2 = 7.10\) at \(45^\circ \mathrm{C}\) 3. We need to find \(K_3\), the equilibrium constant for the reaction: \(C(g) + D(g) \rightleftharpoons 2B(g)\)
02

Manipulate the given reactions to obtain the target reaction

First, we will multiply the first reaction by 2, to make the number of A's equal to the second reaction, resulting in: \[2A(g) + 2B(g) \rightleftharpoons 2C(g) \quad (1')\] Now, we can subtract the second reaction from the first reaction (1'): \((1') - (2) \Rightarrow )[2A(g) + 2B(g) \rightleftharpoons 2C(g)] - [2A(g) + D(g) \rightleftharpoons C(g)]\] Which results in the target reaction: \[C(g) + D(g) \rightleftharpoons 2B(g)\]
03

Apply the rule for equilibrium constants of the manipulated reactions and find the \(K_3\)

When we multiplied the first reaction by 2, the new equilibrium constant becomes \(K_1^{'} = K_1^2\), so we get: \(K_1^{'} = 3.50^2 = 12.25\) When we subtracted the second reaction from the first reaction, the new equilibrium constant will be the quotient of the two constants \(K_3 = \frac{K_1^{'}}{K_2}\), so we have: \(K_3 = \frac{12.25}{7.10} = 1.725\) So, the value of \(K_3\) at the same temperature for the reaction \(C(g) + D(g) \rightleftharpoons 2B(g)\) is 1.725.
04

Calculate the mole fraction of B at equilibrium

We are given that the initial partial pressures of C and D are both 1.50 atm. Let the change in pressure of B at equilibrium be denoted as \(x\). Then, the pressure of B at equilibrium will be \(2x\), and the pressure of C and D will be \(1.50 - x\) atm each. The reaction quotient, \(Q_p\), for the target reaction can be written as: \(Q_p = \frac{P^2_{B}}{P_{C} \cdot P_{D}}\) At equilibrium, \(Q_p\) is equal to \(K_p\). Thus, \(K_p = \frac{(2x)^2}{(1.50 - x)(1.50 - x)}\) We are given that \(K_p = K_3 = 1.725\), so: \(1.725 = \frac{4x^2}{(1.50 - x)^2}\) Now, we will solve for \(x\). Since we are looking for the mole fraction of B, which must be less than 1, we can discard any extraneous solutions. \(x \approx 0.468\) The mole fraction of B at equilibrium is: \[\frac{2x}{1.50 + 1.50} = \frac{2(0.468)}{3.00} \approx 0.312\] Thus, the mole fraction of B once equilibrium is reached is approximately 0.312.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Chemical Equilibrium
Chemical equilibrium refers to the state in which the concentrations of reactants and products in a chemical reaction remain constant over time.
This happens when the forward and reverse reactions occur at the same rate. In an equilibrium state, the reaction doesn't stop; both directions continue to proceed, but there's no net change in the concentrations. Equilibrium can be reached in both closed and open systems.
For a reaction like \[ A(g) + B(g) \rightleftharpoons C(g), \]if the system reaches equilibrium, the rate at which A and B form C is equal to the rate at which C decomposes back into A and B.
  • The equilibrium constant, \( K \), gives us the ratio of the concentrations of products to reactants at equilibrium, allowing us to understand the extent of a reaction under given conditions.
Reaction Quotient
The reaction quotient \( Q \) is a tool used to determine the direction in which a chemical reaction will proceed.
It's similar to the equilibrium constant \( K \) but can be calculated at any point in time, not just at equilibrium.
To find \( Q \), use the same formula as \( K \), substituting the current concentrations or pressures of the reactants and products. If a reaction is in the form:\[ C(g) + D(g) \rightleftharpoons 2B(g), \]you calculate \( Q \) as:\[ Q = \frac{P_B^2}{P_C \cdot P_D}. \]
  • If \( Q > K \), the reaction will shift to the left to reach equilibrium.
  • If \( Q < K \), the reaction will shift to the right.
  • If \( Q = K \), the system is at equilibrium.

This tool is essential when predicting how a system will behave when conditions change.
Partial Pressures
Partial pressures refer to the pressure contributed by each individual gas in a mixture.
In a chemical reaction involving gases, each gas behaves independently and contributes to the total pressure.
This concept is crucial when working with equilibrium calculations involving gases. For a mixture containing gases C, D, and B, partial pressures are used to calculate the equilibrium constant expression.
If initial partial pressures are given, like 1.50 atm for both C and D, they help in setting up equations to find changes in pressure during the reaction.
For the reaction: \[ C(g) + D(g) \rightleftharpoons 2B(g), \]the partial pressures of each gas allow us to solve for the equilibrium position using: \[ K_p = \frac{P_B^2}{P_C \cdot P_D}, \]where \( P_B, P_C, \) and \( P_D \) are the equilibrium pressures of B, C, and D, respectively.
Mole Fraction
The mole fraction is a way of expressing the concentration of a component in a mixture.
It is defined as the ratio of the moles of one component to the total moles in the mixture.
In a chemical equilibrium problem, understanding mole fractions helps determine concentrations of gases relative to each other. For the reaction \[ C(g) + D(g) \rightleftharpoons 2B(g), \]if the equilibrium condition changes the pressures of C and D from 1.50 atm to 1.50 - x atm, and the pressure of B to 2x atm, the mole fraction of B is given by:
  • \( \text{Mole fraction of } B = \frac{2x}{1.50 + 1.50} \).

This reflects B's proportion in the total pressure of the system. Mole fractions are dimensionless and valuable in determining reaction outcomes.

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Most popular questions from this chapter

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 \(250 . \mathrm{C} .\)

The synthesis of ammonia gas from nitrogen gas and hydrogen gas represents a classic case in which a knowledge of kinetics and equilibrium was used to make a desired chemical reaction economically feasible. Explain how each of the following conditions helps to maximize the yield of ammonia. a. running the reaction at an elevated temperature b. removing the ammonia from the reaction mixture as it forms c. using a catalyst d. running the reaction at high pressure

A sample of \(\mathrm{S}_{8}(g)\) is placed in an otherwise empty rigid container at 1325 \(\mathrm{K}\) at an initial pressure of \(1.00 \mathrm{atm},\) where it decomposes to \(\mathrm{S}_{2}(g)\) by the reaction $$\mathrm{S}_{8}(g) \rightleftharpoons 4 \mathrm{S}_{2}(g)$$ At equilibrium, the partial pressure of \(\mathrm{S}_{8}\) is 0.25 atm. Calculate \(K_{\mathrm{p}}\) for this reaction at 1325 \(\mathrm{K}\) .

At \(25^{\circ} \mathrm{C}, K=0.090\) for the reaction $$\mathrm{H}_{2} \mathrm{O}(g)+\mathrm{Cl}_{2} \mathrm{O}(g) \rightleftharpoons 2 \mathrm{HOCl}(g)$$ Calculate the concentrations of all species at equilibrium for each of the following cases. a. 1.0 \(\mathrm{g} \mathrm{H}_{2} \mathrm{O}\) and 2.0 \(\mathrm{g} \mathrm{Cl}_{2} \mathrm{O}\) are mixed in a 1.0 -L flask. b. 1.0 mole of pure HOCl is placed in a 2.0 \(\mathrm{L}\) flask.

For the following endothermic reaction at equilibrium: $$2 \mathrm{SO}_{3}(g) \rightleftharpoons 2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g)$$ which of the following changes will increase the value of \(K ?\) a. increasing the temperature b. decreasing the temperature c. removing \(\mathrm{SO}_{3}(g)\) (constant \(T )\) d. decreasing the volume (constant \(T )\) e. adding \(\operatorname{Ne}(g)(\text { constant } T)\) f. adding \(\mathrm{SO}_{2}(g)(\text { constant } T)\) g. adding a catalyst (constant T)

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