/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 61 A A sample of \(\mathrm{N}_{2} \... [FREE SOLUTION] | 91Ó°ÊÓ

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A A sample of \(\mathrm{N}_{2} \mathrm{O}_{4}\) gas with a pressure of \(1.00 \mathrm{atm}\) is placed in a flask. When equilibrium is achieved, \(20.0 \%\) of the \(\mathrm{N}_{2} \mathrm{O}_{4}\) has been converted to \(\mathrm{NO}_{2}\) gas. (a) Calculate \(K_{\mathrm{p}}\) (b) If the original pressure of \(\mathrm{N}_{2} \mathrm{O}_{4}\) is 0.10 atm, what is the percent dissociation of the gas? Is the result in agree. ment with Le Chatelier's principle?

Short Answer

Expert verified
(a) \(K_p = 0.20\). (b) Percent dissociation = 45%; aligns with Le Chatelier's principle.

Step by step solution

01

Write the equilibrium reaction

The dissociation of \(\mathrm{N}_{2} \mathrm{O}_{4}\) gas into \(\mathrm{NO}_{2}\) is represented by the following reaction: \[\mathrm{N}_{2} \mathrm{O}_{4}(g) \rightleftharpoons 2\mathrm{NO}_{2}(g)\]
02

Determine the change in moles at equilibrium (Part a)

Let the initial pressure of \(\mathrm{N}_{2} \mathrm{O}_{4}\) be \(1.00 \mathrm{atm}\). If \(20\%\) is dissociated, the change in pressure for \(\mathrm{N}_{2} \mathrm{O}_{4}\) is \(0.20 \times 1.00 = 0.20 \mathrm{atm}\). This produces \(2 \times 0.20 = 0.40 \mathrm{atm}\) of \(\mathrm{NO}_{2}\).
03

Calculate equilibrium pressures (Part a)

At equilibrium, the pressure of \(\mathrm{N}_{2} \mathrm{O}_{4}\) is \(1.00 - 0.20 = 0.80 \mathrm{atm}\), and the pressure of \(\mathrm{NO}_{2}\) is \(0.40 \mathrm{atm}\).
04

Calculate Kp for the equilibrium (Part a)

The equilibrium constant \( K_p \) can be calculated using the equation \[ K_p = \frac{(P_{\mathrm{NO}_{2}})^2}{P_{\mathrm{N}_{2} \mathrm{O}_{4}}} \] Substituting the equilibrium pressures yields \[ K_p = \frac{(0.40)^2}{0.80} = \frac{0.16}{0.80} = 0.20 \]
05

Initial setting for Part b

If the initial pressure of \(\mathrm{N}_{2} \mathrm{O}_{4}\) is \(0.10 \mathrm{atm}\), let \(x\) atm be the pressure that dissociates at equilibrium.
06

Set up equilibrium concentrations and expressions (Part b)

The equilibrium pressures are \((0.10 - x)\) atm for \(\mathrm{N}_{2} \mathrm{O}_{4}\) and \(2x\) atm for \(\mathrm{NO}_{2}\). The same \(K_p\) value from Part a applies here: \[ 0.20 = \frac{(2x)^2}{0.10 - x} \]
07

Solve the quadratic equation (Part b)

First, substitute and simplify the equation: \[ 0.20(0.10 - x) = 4x^2 \] Leading to \[ 0.02 - 0.20x = 4x^2 \] Rewriting, we have \[ 4x^2 + 0.20x - 0.02 = 0 \] Solve it using the quadratic formula \(x = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a}\) with \(a = 4, b = 0.20, c = -0.02\).
08

Calculate percent dissociation and check Le Chatelier's principle (Part b)

Solving, we find that \(x \approx 0.045 \). Therefore, the percent dissociation is \(\frac{x}{0.10} \times 100 = 45\%\). At lower pressure, a higher percentage dissociation occurs, agreeing with Le Chatelier's principle.

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Key Concepts

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

Le Chatelier's Principle
Le Chatelier's principle is a fundamental concept in chemistry, providing insight into how chemical equilibria respond to external changes. If a system in equilibrium experiences a change in concentration, pressure, or temperature, it will adjust itself to counteract the effect and re-establish equilibrium. For instance, if the pressure of a gaseous reaction is decreased, the system will shift the equilibrium position to increase the number of gas particles, effectively increasing pressure.
This principle is particularly useful in predicting the behavior of reactions under different conditions. It explains why, in our exercise, a reduction in the initial pressure of \(\mathrm{N}_{2} \mathrm{O}_{4}\), leads to a higher percent dissociation. At lower pressures, the shift of equilibrium towards the right side (formation of more gas particles \(\mathrm{NO}_{2}\)) is favored according to Le Chatelier's principle, aiming to restore pressure.
Equilibrium Constant (Kp)
The equilibrium constant for a reaction involving gases, denoted as \(K_p\), is a measure of the ratio of the pressures of products to reactants at equilibrium, each raised to the power of their respective coefficients in the balanced chemical equation. This constant provides crucial information about the position of equilibrium; larger values of \(K_p\) indicate a predominance of products, while smaller values suggest a predominance of reactants at equilibrium.
In the given exercise, the equilibrium constant \(K_p\) for the reaction \[ \mathrm{N}_{2} \mathrm{O}_{4}(g) \rightleftharpoons 2\mathrm{NO}_{2}(g) \] was calculated using the pressures of \(\mathrm{NO}_{2}\) and \(\mathrm{N}_{2} \mathrm{O}_{4}\) at equilibrium. With the relationship \[ K_p = \frac{(P_{\mathrm{NO}_{2}})^2}{P_{\mathrm{N}_{2} \mathrm{O}_{4}}} = \frac{0.16}{0.80} = 0.20 \] it confirms the state of balance between products and reactants.
Percent Dissociation
Percent dissociation is a measure of how much a specific compound breaks down into its constituents compared to its initial concentration or pressure. This is particularly relevant for equilibrium reactions, where not all reactants completely dissociate. The percent dissociation is calculated by dividing the amount dissociated by the initial amount, then multiplying by 100 to convert it to a percentage.
For the reaction \(\mathrm{N}_{2} \mathrm{O}_{4} \rightleftharpoons 2\mathrm{NO}_{2}\), in our exercise, the initial sample has a dissociation percentage that changes with pressure. Initially, at 1.00 atm pressure, 20% of \(\mathrm{N}_{2} \mathrm{O}_{4}\) dissociates at equilibrium. When the pressure is reduced to 0.10 atm, the percent dissociation increases to 45%, illustrating the impact of pressure on equilibrium. This elucidates how equilibrium constants help predict the degree of dissociation under varying conditions.

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Most popular questions from this chapter

\(K_{c}\) for the decomposition of ammonium hydrogen sulfide is \(1.8 \times 10^{-4}\) at \(25^{\circ} \mathrm{C}\) $$ \mathrm{NH}_{4} \mathrm{HS}(\mathrm{s}) \rightleftarrows \mathrm{NH}_{3}(\mathrm{g})+\mathrm{H}_{2} \mathrm{S}(\mathrm{g}) $$ (a) When the pure salt decomposes in a flask, what are the equilibrium concentrations of \(\mathrm{NH}_{3}\) and \(\mathrm{H}_{2} \mathrm{S} ?\) (b) If \(\mathrm{NH}_{1} \mathrm{HS}\) is placed in a flask already containing \(0.020 \mathrm{mol} / \mathrm{L}\) of \(\mathrm{NH}_{3}\) and then the system is allowed to come to equilibrium, what are the equilibrium concentrations of \(\mathrm{NH}_{3}\) and \(\mathrm{H}_{2} \mathrm{S} ?\)

Hemoglobin (Hb) can form a complex with both \(\mathrm{O}_{2}\) and CO. For the reaction $$ \mathrm{HbO}_{2}(\mathrm{aq})+\mathrm{CO}(\mathrm{g}) \rightleftarrows \mathrm{HbCO}(\mathrm{aq})+\mathrm{O}_{2}(\mathrm{g}) $$ 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 \(\mathrm{O}_{2}\) is \(0.20 \mathrm{atm}\).

Calculate \(K\) for the reaction $$ \mathrm{Fe}(\mathrm{s})+\mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \rightleftarrows \mathrm{FeO}(\mathrm{s})+\mathrm{H}_{2}(\mathrm{g}) $$ given the following information: $$ \begin{aligned} \mathrm{H}_{2} \mathrm{O}(\mathrm{g})+\mathrm{CO}(\mathrm{g}) & \rightleftarrows \mathrm{H}_{2}(\mathrm{g})+\mathrm{CO}_{2}(\mathrm{g}) & & K=1.6 \\ \mathrm{FeO}(\mathrm{s})+\mathrm{CO}(\mathrm{g}) & \rightleftarrows \mathrm{Fe}(\mathrm{s})+\mathrm{CO}_{2}(\mathrm{g}) & & K=0.67 \end{aligned} $$

The equilibrium constant for the reaction $$ \mathrm{N}_{2} \mathrm{O}_{4}(\mathrm{g}) \rightleftarrows 2 \mathrm{NO}_{2}(\mathrm{g}) $$ at \(25^{\circ} \mathrm{C}\) is \(5.88 \times 10^{-3} .\) Suppose \(15.6 \mathrm{g}\) of \(\mathrm{N}_{2} \mathrm{O}_{4}\) is placed in a \(5.00-\) L. flask at \(25^{\circ}\) C. Calculate the following: (a) the amount of \(\mathrm{NO}_{2}(\mathrm{mol})\) present at equilibrium (b) the percentage of the original \(\mathrm{N}_{2} \mathrm{O}_{4}\) that is dissociated

Ammonium iodide dissociates reversibly to ammonia and hydrogen iodide if the salt is heated to a sufficiently high temperature. $$ \mathrm{NH}_{4} \mathrm{I}(\mathrm{s}) \rightleftarrows \mathrm{NH}_{3}(\mathrm{g})+\mathrm{HI}(\mathrm{g}) $$ Some ammonium iodide is placed in a flask, which is then heated to \(400^{\circ} \mathrm{C}\). If the total pressure in the flask when equilibrium has been achieved is \(705 \mathrm{mm} \mathrm{Hg},\) what is the value of \(K_{\mathrm{p}}\) (when partial pressures are in atmospheres)?

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