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The total pressure for a mixture of \(\mathrm{N}_{2} \mathrm{O}_{4}\) and \(\mathrm{NO}_{2}\) is 0.15 atm. If \(K_{p}=7.1\) (at \(25^{\circ} \mathrm{C}\) ), calculate the partial pressure of each gas in the mixture. $$ 2 \mathrm{NO}_{2}(\mathrm{g}) \rightleftharpoons \mathrm{N}_{2} \mathrm{O}_{4}(\mathrm{g}) $$

Short Answer

Expert verified
\( P_{\text{NO}_2} = 0.066 \text{ atm}, \) \( P_{\text{N}_2\text{O}_4} = 0.084 \text{ atm} \).

Step by step solution

01

Write the Expression for Kp

For the equilibrium reaction \(2 \text{NO}_2(g) \rightleftharpoons \text{N}_2\text{O}_4(g)\), the equilibrium constant expression in terms of partial pressures is: \[ K_p = \frac{P_{\text{N}_2\text{O}_4}}{(P_{\text{NO}_2})^2} \] where \(P_{\text{N}_2\text{O}_4}\) and \(P_{\text{NO}_2}\) are the partial pressures of \(\text{N}_2\text{O}_4\) and \(\text{NO}_2\) respectively.
02

Express Total Pressure

The given total pressure of the gas mixture is the sum of the partial pressures of \(\text{N}_2\text{O}_4\) and \(\text{NO}_2\). Therefore, we have: \[ P_{\text{N}_2\text{O}_4} + P_{\text{NO}_2} = 0.15 \text{ atm} \]
03

Substitute Expressions into Kp Equation

We can use the substitution method to find either \( P_{\text{N}_2\text{O}_4} \) or \( P_{\text{NO}_2} \). Let’s express \( P_{\text{N}_2\text{O}_4} \) in terms of \( P_{\text{NO}_2} \) using the total pressure equation: \[ P_{\text{N}_2\text{O}_4} = 0.15 - P_{\text{NO}_2} \] Substituting into the Kp equation gives: \[ K_p = \frac{0.15 - P_{\text{NO}_2}}{(P_{\text{NO}_2})^2} = 7.1 \]
04

Solve for Partial Pressure of NO2

Rearrange the equation to express in terms of \( P_{\text{NO}_2} \): \[ 7.1(P_{\text{NO}_2})^2 = 0.15 - P_{\text{NO}_2} \] Solving this quadratic equation: \[ 7.1x^2 + x - 0.15 = 0 \] where \( x = P_{\text{NO}_2} \). Use the quadratic formula \( x = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a} \) with \( a = 7.1 \), \( b = 1 \), \( c = -0.15 \).
05

Calculate Roots Using Quadratic Formula

Compute the discriminant \( b^2 - 4ac = 1^2 - 4 \times 7.1 \times (-0.15) \). Calculate: \[ x = \frac{-1 \pm \sqrt{1 + 4.26}}{2 \times 7.1} = \frac{-1 \pm \sqrt{5.26}}{14.2} \] Solve for the positive root (since pressure cannot be negative).
06

Determine Partial Pressures

Calculate the positive root from the earlier step to find \( P_{\text{NO}_2} \). After computation, \( P_{\text{NO}_2} \approx 0.066 \text{ atm} \). Use the total pressure to find \( P_{\text{N}_2\text{O}_4} = 0.15 - 0.066 = 0.084 \text{ atm} \).

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Key Concepts

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

Partial Pressure
When dealing with gas mixtures, understanding partial pressure is essential. Each gas in a mixture exerts pressure independently of the others. This pressure, known as partial pressure, represents how much pressure a particular gas contributes to the total pressure of the mixture.

In the context of chemical equilibria, it's important to remember that the total pressure of the system is the sum of the partial pressures of all gases present. For our exercise, the total pressure is given as 0.15 atm, comprising the partial pressures of \( ext{N}_2 ext{O}_4\) and \( ext{NO}_2\). Hence, you set up the equation: \[ P_{\text{N}_2\text{O}_4} + P_{\text{NO}_2} = 0.15 \text{ atm} \] This forms the basis for calculating the individual partial pressures of the gases.
Equilibrium Constant
The concept of the equilibrium constant \(K_p\) is central in chemical equilibria, especially for gaseous systems. It provides insight into the position of equilibrium at a given temperature.

For the reaction \(2 \text{NO}_2(g) \rightleftharpoons \text{N}_2\text{O}_4(g)\), \(K_p\) is expressed in terms of the partial pressures of the reactants and products as follows: \[ K_p = \frac{P_{\text{N}_2\text{O}_4}}{(P_{\text{NO}_2})^2} \]

Here, \(K_p\) value of 7.1 indicates that at equilibrium, the pressure of \( ext{N}_2 ext{O}_4\) relative to \(\text{NO}_2\) squared is consistent, as dictated by this constant. The equilibrium constant helps predict how the reaction shifts in response to changes in conditions, vital for understanding the dynamic nature of equilibrium.
Quadratic Formula
To determine the individual partial pressures of gases in our equilibrium system, the quadratic formula is employed. Quadratic equations often arise in chemical equilibrium problems when expressing \(K_p\).

In this case, substituting into the \(K_p\) equation gives a quadratic equation that can be expressed as: \[ 7.1(P_{\text{NO}_2})^2 = 0.15 - P_{\text{NO}_2} \] Rearranging gives the quadratic form: \[ 7.1x^2 + x - 0.15 = 0 \] where \( x = P_{\text{NO}_2} \).
  • \(a = 7.1\)
  • \(b = 1\)
  • \(c = -0.15\)
The quadratic formula, \[ x = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a} \] is then used to find the possible values of \(x\). Solving this gives the partial pressures required for the exercise.
Gaseous Equilibria
Gaseous equilibria involve reactions in which all reactants and products are gases. These systems are influenced by changes in pressure, volume, and temperature. When a system reaches equilibrium, the forward and reverse reactions occur at equal rates, stabilizing concentrations or pressures over time.

In our reaction \(2 \text{NO}_2(g) \rightleftharpoons \text{N}_2\text{O}_4(g)\), the system reacts to establish a dynamic balance, characterized by the equilibrium constant \(K_p\). It's crucial to consider that changes in conditions such as pressure will shift the equilibrium position—a concept explained by Le Chatelier’s Principle.

Understanding these principles allows chemists to manipulate conditions to favor the formation of desired products, an application valuable in industrial and laboratory settings.

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Most popular questions from this chapter

Suppose a tank initially contains \(\mathrm{H}_{2} \mathrm{S}\) at a pressure of 10.00 atm and a temperature of 800 K. When the reaction has come to equilibrium, the partial pressure of \(\mathbf{S}_{2}\) vapor is 0.020 atm. Calculate \(K_{\mathrm{p}}\) $$ 2 \mathrm{H}_{2} \mathrm{S}(\mathrm{g}) \rightleftharpoons 2 \mathrm{H}_{2}(\mathrm{g})+\mathrm{S}_{2}(\mathrm{g}) $$

Describe an experiment that would allow you to prove that the system \(3 \mathrm{H}_{2}(\mathrm{g})+\mathrm{N}_{2}(\mathrm{g}) \rightleftharpoons 2$$\mathrm{NH}_{3}(\mathrm{g})\) is a dynamic equilibrium. (Hint: Consider using a stable isotope such as \(^{15} \mathrm{N}\) or \(^{2} \mathrm{H} .\) )

You place 0.0300 mol of pure \(\mathrm{SO}_{3}\) in an \(8.00-\mathrm{L}\) flask at \(1150 \mathrm{K}\). At equilibrium, 0.0058 mol of \(\mathrm{O}_{2}\) has been formed. Calculate \(K_{c}\) for the reaction at \(1150 \mathrm{K}\) $$ 2 \mathrm{sO}_{3}(\mathrm{g}) \rightleftharpoons 2 \mathrm{sO}_{2}(\mathrm{g})+\mathrm{O}_{2}(\mathrm{g}) $$

Hemoglobin (Hb) can form a complex with both \(\mathrm{O}_{2}\) and \(\mathrm{CO}\). For the reaction $$ \mathrm{HbO}_{2}(\mathrm{aq})+\mathrm{CO}(\mathrm{g}) \rightleftharpoons \mathrm{HbCO}(\mathrm{aq})+\mathrm{O}_{2}(\mathrm{g}) $$ at body temperature, \(K\) is about \(200 .\) If the ratio \(|\mathrm{HbCO}| /\left|\mathrm{HbO}_{2}\right|\) comes close to \(1,\) death is probable. What partial pressure of CO in the air is likely to be fatal? Assume the partial pressure of \(\mathbf{O}_{2}\) is \(0.20 \mathrm{atm}\)

Write equilibrium constant expressions for the following reactions. For gases, use either pressures or concentrations. (a) \(2 \mathrm{H}_{2} \mathrm{O}_{2}(\mathrm{g}) \rightleftharpoons 2 \mathrm{H}_{2} \mathrm{O}(\mathrm{g})+\mathrm{O}_{2}(\mathrm{g})\) (b) \(\mathrm{CO}(\mathrm{g})+1 / 2 \mathrm{O}_{2}(\mathrm{g}) \rightleftharpoons \mathrm{CO}_{2}(\mathrm{g})\) (c) \(\mathrm{C}(\mathrm{s})+\mathrm{CO}_{2}(\mathrm{g}) \rightleftharpoons 2 \mathrm{CO}(\mathrm{g})\) (d) \(\mathrm{NiO}(\mathrm{s})+\mathrm{CO}(\mathrm{g}) \rightleftharpoons \mathrm{Ni}(\mathrm{s})+\mathrm{CO}_{2}(\mathrm{g})\)

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