/*! 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 108 Sulfuric acid is produced in lar... [FREE SOLUTION] | 91Ó°ÊÓ

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Sulfuric acid is produced in larger amounts by weight than any other chemical. It is used in manufacturing fertilizers, oil refining, and hundreds of other processes. An intermediate step in the industrial process for the synthesis of \(\mathrm{H}_{2} \mathrm{SO}_{4}\) is the catalytic oxidation of sulfur dioxide: $$2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{SO}_{3}(g) \quad \Delta G^{\circ}=-141.8 \mathrm{~kJ}$$ Calculate \(\Delta G\) at \(25^{\circ} \mathrm{C}\), given the following sets of partial pressures: (a) \(100 \mathrm{~atm} \mathrm{SO}_{2}, 100 \mathrm{~atm} \mathrm{O}_{2}, 1.0 \mathrm{~atm} \mathrm{SO}_{3}\) (b) \(2.0 \mathrm{~atm} \mathrm{SO}_{2}, 1.0 \mathrm{~atm} \mathrm{O}_{2}, 10 \mathrm{~atm} \mathrm{SO}_{3}\) (c) Each reactant and product at a partial pressure of \(1.0 \mathrm{~atm}\)

Short Answer

Expert verified
(a) \( \Delta G = +198.8 \text{ kJ}\); (b) \( \Delta G = -141.7 \text{ kJ}\); (c) \( \Delta G = -141.8 \text{ kJ}\).

Step by step solution

01

Understand the Reaction

The reaction given is the oxidation of sulfur dioxide: \(2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \rightarrow 2 \mathrm{SO}_{3}(g)\). The standard Gibbs free energy change \( \Delta G^{\circ} \) is \(-141.8 \mathrm{~kJ}\).
02

Identify the Formula for \( \Delta G \)

The Gibbs free energy change \( \Delta G \) is calculated using the formula: \( \Delta G = \Delta G^{\circ} + RT \ln Q \), where \( R \) is the ideal gas constant \(8.314 \text{ J/mol K}\), \( T \) is the temperature in Kelvin, and \( Q \) is the reaction quotient.
03

Calculate \( Q \) for Each Scenario

The reaction quotient \( Q \) is given by \( Q = \frac{{(P_{\mathrm{SO}_3})^2}}{{(P_{\mathrm{SO}_2})^2 (P_{\mathrm{O}_2})}} \). Calculate \( Q \) for each set of conditions given.
04

Step 4a: Calculate \( \Delta G \) for Condition (a)

For \((a)\), \( P_{\mathrm{SO}_2} = 100 \text{ atm}, \; P_{\mathrm{O}_2} = 100 \text{ atm}, \; P_{\mathrm{SO}_3} = 1.0 \text{ atm}\). Thus, \( Q = \frac{{1.0^2}}{{100^2 \times 100}} \). First, calculate \( Q \) then \( \Delta G \).
05

Step 4b: Calculate \( \Delta G \) for Condition (b)

For \((b)\), \( P_{\mathrm{SO}_2} = 2.0 \text{ atm}, \; P_{\mathrm{O}_2} = 1.0 \text{ atm}, \; P_{\mathrm{SO}_3} = 10 \text{ atm}\). So, \( Q = \frac{{10^2}}{{2.0^2 \times 1.0}} \). Calculate \( Q \) and then \( \Delta G \).
06

Step 4c: Calculate \( \Delta G \) for Condition (c)

For \((c)\), \( P_{\mathrm{SO}_2} = P_{\mathrm{O}_2} = P_{\mathrm{SO}_3} = 1.0 \text{ atm}\). Hence, \( Q = \frac{{1.0^2}}{{1.0^2 \times 1.0}} = 1 \). Calculate \( \Delta G \).
07

Perform Calculations for \( \Delta G \)

Use the formula \( \Delta G = \Delta G^{\circ} + RT \ln Q \) with \( R = 8.314 \text{ J/mol K} \) and \( T = 298 \text{ K} \) to calculate \( \Delta G \) for each part. Convert \( \Delta G \) from Joules to kilojoules by dividing by 1000.

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Key Concepts

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

Sulfuric Acid Production
Sulfuric acid (\( \text{H}_{2}\text{SO}_{4} \)) is a critical component in numerous industrial processes. It is predominantly used in the manufacture of fertilizers but also finds applications in oil refining, wastewater treatment, and chemical synthesis. The production of sulfuric acid is driven by its demand due to its capability to react with various substances, enhancing reaction efficiency and output.
The process typically involves several steps, with one of the crucial steps being the conversion of sulfur dioxide (\( \text{SO}_{2} \)) to sulfur trioxide (\( \text{SO}_{3} \)) through catalytic oxidation. This serves as a precursor to form sulfuric acid when combined with water. Efficiency and environmental considerations make this step fundamental in the overall production cycle.
Catalytic Oxidation
Catalytic oxidation is vital in transforming sulfur dioxide (\( \text{SO}_{2} \)) into sulfur trioxide (\( \text{SO}_{3} \)), a precursor for sulfuric acid. This reaction uses a catalyst, often vanadium(V) oxide (\( \text{V}_{2}\text{O}_{5} \)), to lower the activation energy and speed up the conversion. Without a catalyst, the reaction would be too slow and inefficient for commercial purposes.
  • The catalyst provides a surface for the reaction, enabling more frequent and successful collisions between reactant molecules.
  • It allows the reaction to proceed at a lower temperature and pressure than would otherwise be necessary.
Catalytic oxidation is carefully controlled to optimize yield and minimize environmental impact, contributing to the industrial sector's sustainability.
Reaction Quotient
The reaction quotient (\( Q \)) is a measure used to predict the direction and extent of a chemical reaction at any given point during its progress. For the reaction converting sulfur dioxide to sulfur trioxide, \( Q \) is calculated as follows:\[Q = \frac{{(P_{\text{SO}_{3}})^{2}}}{{(P_{\text{SO}_{2}})^{2} \cdot (P_{\text{O}_{2}})}}\]This formula compares the pressure of the products to that of the reactants. When \( Q \) is less than the equilibrium constant (\( K \)), the forward reaction is favored, meaning the reaction will continue producing more products to reach equilibrium.
In industrial setups, maintaining the appropriate pressure conditions as dictated by \( Q \) ensures optimal conversion rates in the production of sulfur trioxide.
Ideal Gas Constant
The ideal gas constant (\( R \)) is a key component in thermodynamics, especially in the calculation of Gibbs Free Energy (\( \Delta G \)). In the formula \( \Delta G = \Delta G^{\circ} + RT \ln Q \), it bridges physical constants with practical conditions under which reactions occur.
The constant \( R \) is valued at 8.314 J/mol K and helps convert energy into understandable terms relating to temperature and reaction conditions.
Using \( R \), calculations consider how temperature and reaction quotient (\( Q \)) influence the Gibbs Free Energy, determining spontaneity and feasibility. This is crucial in real-world applications, where adjustments to temperature or pressure can significantly influence reaction outcomes. Understanding \( R \) ensures control over industrial chemical processes, enhancing efficiency and reducing costs.

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Most popular questions from this chapter

Consider a disordered crystal of monodeuteriomethane in which each tetrahedral \(\mathrm{CH}_{3} \mathrm{D}\) molecule is oriented randomly in one of four possible ways. Use Boltzmann's equation to calculate the entropy of the disordered state of the crystal if the crystal contains: (a) 12 molecules (b) 120 molecules (c) 1 mol of molecules (d) What is the entropy of the crystal if the \(C-D\) bond of each of the \(\mathrm{CH}_{3} \mathrm{D}\) molecules points in the same direction?

The standard free-energy change at \(25^{\circ} \mathrm{C}\) for the dissociation of water is \(79.9 \mathrm{~kJ}\) : $$2 \mathrm{H}_{2} \mathrm{O}(l) \rightleftharpoons \mathrm{H}_{3} \mathrm{O}^{+}(a q)+\mathrm{OH}^{-}(a q) \quad \Delta G^{\circ}=79.9 \mathrm{~kJ}$$ For each of the following sets of concentrations, calculate \(\Delta G\) at \(25^{\circ} \mathrm{C}\) and indicate whether the reaction is spontaneous in the forward or reverse direction: (a) \(\left[\mathrm{H}_{3} \mathrm{O}^{+}\right]=\left[\mathrm{OH}^{-}\right]=1.0 \mathrm{M}\) (b) \(\left[\mathrm{H}_{3} \mathrm{O}^{+}\right]=\left[\mathrm{OH}^{-}\right]=1.0 \times 10^{-7} \mathrm{M}\) (c) \(\left[\mathrm{H}_{3} \mathrm{O}^{+}\right]=1.0 \times 10^{-7} \mathrm{M},\left[\mathrm{OH}^{-}\right]=1.0 \times 10^{-10} \mathrm{M}\) Are your results consistent with Le Châtelier's principle? Use the thermodynamic data to calculate the equilibrium constant for the reaction.

Reduction of mercury(II) oxide with zinc gives metallic mercury: $$\mathrm{HgO}(s)+\mathrm{Zn}(s) \longrightarrow \mathrm{ZnO}(s)+\mathrm{Hg}(l)$$ (a) If \(\Delta H^{\circ}=-259.7 \mathrm{~kJ} / \mathrm{mol}\) and \(\Delta S^{\circ}=+7.8 \mathrm{~J} / \mathrm{K}\), what is \(\Delta S_{\text {total }}\) for this reaction? Is the reaction spontaneous under standard-state conditions at \(25^{\circ} \mathrm{C} ?\) (b) Estimate at what temperature, if any, the reaction will become nonspontaneous.

By what factor does the entropy increase for a collection of 1000 molecules moved from \(1.00 \times 10^{6}\) boxes to \(1.00 \times 10^{7}\) boxes? For a move from \(1.00 \times 10^{16}\) to \(1.00 \times 10^{17}\) boxes? (Express your answers to three significant figures.)

For the vaporization of benzene, \(\Delta H_{\text {vap }}=30.7 \mathrm{~kJ} / \mathrm{mol}\) and \(\Delta S_{\text {vap }}=87.0 \mathrm{~J} /(\mathrm{K} \cdot \mathrm{mol}) .\) Calculate \(\Delta S_{\text {surr }}\) and \(\Delta S_{\text {total }}\) at: (a) \(70^{\circ} \mathrm{C}\) (b) \(80^{\circ} \mathrm{C}\) (c) \(90^{\circ} \mathrm{C}\) Does benzene boil at \(70^{\circ} \mathrm{C}\) and 1 atm pressure? Calculate the normal boiling point of benzene.

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