Explain qualitatively how \(\Delta G\) changes for each of the following reactions as the partial pressure of \(\mathrm{O}_{2}\) is increased: (a) \(2 \mathrm{CO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g)\) (b) \(2 \mathrm{H}_{2} \mathrm{O}_{2}(l) \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{O}_{2}(g)\) (c) \(2 \mathrm{KClO}_{3}(s) \longrightarrow 2 \mathrm{KCl}(s)+3 \mathrm{O}_{2}(g)\)

Short Answer

Expert verified
For each reaction: (a) As the partial pressure of \(O_{2}\) increases, the reaction will shift towards the products, making it more spontaneous and causing \(\Delta G\) to decrease. (b) With an increased partial pressure of \(O_{2}\), the reaction will shift towards the reactants, resulting in a decrease in spontaneity and an increase in \(\Delta G\). (c) Similar to reaction (b), increasing the partial pressure of \(O_{2}\) will shift the reaction towards the reactants, leading to a decrease in spontaneity and an increase in \(\Delta G\).

Step by step solution

01

ΔG is the Gibbs free energy change, which can be used to determine the spontaneity of a reaction. Mathematically, ΔG is related to the equilibrium constant (K) and the reaction quotient (Q) by the equation: \[ ΔG = ΔG^⦵ + RT\ln(Q) \] where ΔG^⦵ is the standard free energy change, R is the gas constant, and T is the temperature in Kelvin. As the partial pressure of O₂ changes, so will Q, causing ΔG to vary. We will apply Le Chatelier's principle, which states that when a system at equilibrium is subjected to a change in pressure, temperature, or concentration, it will shift to counteract the change and restore equilibrium. In this case, we will focus on the effect of increased partial pressure of O₂ on each reaction. #Step 2: Analyze reaction (a) with increased partial pressure of O₂#

The first reaction is given by: \[ 2CO(g) + O₂(g) \longrightarrow 2CO₂(g) \] In this reaction, as we increase the partial pressure of O₂ (a reactant), the reaction will try to counteract the change and restore equilibrium, according to Le Chatelier's principle. This leads to a shift in the reaction towards the products (CO₂). As a result, this reaction will become more spontaneous, meaning that ΔG will decrease. #Step 3: Analyze reaction (b) with increased partial pressure of O₂#
02

The second reaction is given by: \[ 2H₂O₂(l) \longrightarrow 2H₂O(l) + O₂(g) \] In this reaction, increasing the partial pressure of O₂ (a product) leads to a shift in the reaction in order to counteract the change. According to Le Chatelier's principle, the reaction will shift towards the reactants (H₂O₂) in order to restore equilibrium. Consequently, this reaction will become less spontaneous, meaning that ΔG will increase. #Step 4: Analyze reaction (c) with increased partial pressure of O₂#

The third reaction is given by: \[ 2KClO₃(s) \longrightarrow 2KCl(s) + 3O₂(g) \] In this reaction, increasing the partial pressure of O₂ (a product) also causes a shift back towards the reactants (KClO₃), as predicted by Le Chatelier's principle. Therefore, the reaction will become less spontaneous, implying an increase in ΔG.

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Most popular questions from this chapter

When most elastomeric polymers (e.g., a rubber band) are stretched, the molecules become more ordered, as illustrated here: Suppose you stretch a rubber band. (a) Do you expect the entropy of the system to increase or decrease? (b) If the rubber band were stretched isothermally, would heat need to be absorbed or emitted to maintain constant temperature? (c) Try this experiment: Stretch a rubber band and wait a moment. Then place the stretched rubber band on your upper lip, and let it return suddenly to its unstretched state (remember to keep holding on). What do you observe? Are your observations consistent with your answer to part (b)?

(a) For a process that occurs at constant temperature, express the change in Gibbs free energy in terms of changes in the enthalpy and entropy of the system. (b) For a certain process that occurs at constant \(T\) and \(P,\) the value of \(\Delta G\) is positive. What can you conclude? (c) What is the relationship between \(\Delta G\) for a process and the rate at which it occurs?

(a) Using data in Appendix \(C\), estimate the temperature at which the free- energy change for the transformation from \(\mathrm{I}_{2}(s)\) to \(\mathrm{I}_{2}(g)\) is zero. What assumptions must you make in arriving at this estimate? (b) Use a reference source, such as Web Elements (www.webelements.com), to find the experimental melting and boiling points of \(\mathrm{I}_{2} .\) (c) Which of the values in part (b) is closer to the value you obtained in part (a)? Can you explain why this is so?

For the isothermal expansion of a gas into a vacuum, \(\Delta E=0, q=0\), and \(w=0\). (a) Is this a spontaneous process? (b) Explain why no work is done by the system during this process. (c) In thermodynamics, what is the "driving force" for the expansion of the gas?

(a) How can we calculate \(\Delta S\) for an isothermal process? (b) Does \(\Delta S\) for a process depend on the path taken from the initial state to the final state of the system? Explain.

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