\(\mathrm{H}_{2}(\mathrm{g})\) can be prepared by passing steam over hot iron: \(3 \mathrm{Fe}(\mathrm{s})+4 \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \rightleftharpoons \mathrm{Fe}_{3} \mathrm{O}_{4}(\mathrm{s})+4 \mathrm{H}_{2}(\mathrm{g})\) (a) Write an expression for the thermodynamic equilibrium constant for this reaction. (b) Explain why the partial pressure of \(\mathrm{H}_{2}(\mathrm{g})\) is independent of the amounts of \(\mathrm{Fe}(\mathrm{s})\) and \(\mathrm{Fe}_{3} \mathrm{O}_{4}(\mathrm{s})\) present. (c) Can we conclude that the production of \(\mathrm{H}_{2}(\mathrm{g})\) from \(\mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) could be accomplished regardless of the proportions of \(\mathrm{Fe}(\mathrm{s})\) and \(\mathrm{Fe}_{3} \mathrm{O}_{4}(\mathrm{s})\) present? Explain.

Short Answer

Expert verified
a) \(K=[H_{2}]^{4}\) b) The partial pressure of \(H_{2}(g)\) is independent of the amounts of \(Fe(s)\) and \(Fe_{3}O_{4}(s)\) present because these are solids and hence their activities, which are equal to 1, do not enter into the equilibrium constant expression or affect gas-phase partial pressures. c) While the exact proportions of \(Fe(s)\) and \(Fe_{3}O_{4}(s)\) may not impact the equilibrium state of the reaction, they could affect the rate at which this equilibrium state is reached since they act as catalysts.

Step by step solution

01

Expressing the thermodynamic equilibrium constant

The equilibrium constant for the reaction, K, is defined by the concentrations of the products divided by the concentrations of the reactants, each raised to the power of their stoichiometric coefficients. Therefore, given the balanced chemical reaction is: \(3 \, Fe(s)+4 \, H_{2}O(g) \leftrightharpoons Fe_{3} O_{4}(s)+4 \, H_{2}(g)\) For gases and aqueous solutions, '[ ]' represents concentration in mol/L, but for solids and liquids, it represents activity, and their activity is always equal to 1. The equilibrium expression for the reaction becomes: \( K=[H_{2}]^{4}=[H_{2}O]^{0}=[Fe]^{0}=[Fe_{3}O_{4}]^{0}\ K=[H_{2}]^{4} \) Note: The activities of the solid components \(Fe_{3}O_{4}(s)\) and \(Fe_{s}\) are taken as 1 and hence are not considered in the expression for K.
02

Understanding Partial Pressure of \(H_{2}(g)\)

Partial pressures are directly related to the concentrations of the gases involved, so explaining why the partial pressure of \(H_{2}(g)\) is independent of the amounts of \(Fe(s)\) and \(Fe_{3}O_{4}(s)\) present requires understanding the role of these solid substances in the reaction. It's key to note that the amounts of solids neither enter into the equilibrium constant (as we derived above) nor affect the partial pressures of the gases. This is because the activity of a pure solid or liquid phase in a reaction is constant (equal to 1), and therefore independent of the amount present.
03

Assessing the production of \(H_{2}(g)\) from \(H_{2}O(g)\)

The question asks whether the production of \(H_{2}(g)\) from \(H_{2}O(g)\) could be accomplished regardless of the proportions of \(Fe(s)\) and \(Fe_{3}O_{4}(s)\) present. Based on our previous discussion, the amounts of \(Fe(s)\) and \(Fe_{3}O_{4}(s)\) present do not affect the equilibrium constant or the partial pressure of \(H_{2}(g)\). However, while these amounts may not impact the equilibrium condition, they can affect the rate at which equilibrium is reached. Even though the concentrations of the solids do not appear in the equilibrium expression, these solids are catalysts that speed up the reaction rate by offering a surface for the reaction to occur. Therefore, while the production of \(H_{2}(g)\) can theoretically occur regardless of the proportions of solids present, in practice these proportions can affect how quickly that production happens.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

The following standard Gibbs energy changes are given for \(25^{\circ} \mathrm{C}\) (1) \(\mathrm{SO}_{2}(\mathrm{g})+3 \mathrm{CO}(\mathrm{g}) \longrightarrow \operatorname{COS}(\mathrm{g})+2 \mathrm{CO}_{2}(\mathrm{g})\) \(\Delta G^{\circ}=-246.4 \mathrm{kJ}\) (2) \(\mathrm{CS}_{2}(\mathrm{g})+\mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \longrightarrow \operatorname{COS}(\mathrm{g})+\mathrm{H}_{2} \mathrm{S}(\mathrm{g})\) \(\Delta G^{\circ}=-41.5 \mathrm{kJ}\) (3) \(\mathrm{CO}(\mathrm{g})+\mathrm{H}_{2} \mathrm{S}(\mathrm{g}) \longrightarrow \operatorname{COS}(\mathrm{g})+\mathrm{H}_{2}(\mathrm{g})\) \(\Delta G^{\circ}=+1.4 \mathrm{kJ}\) (4) \(\mathrm{CO}(\mathrm{g})+\mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \longrightarrow \mathrm{CO}_{2}(\mathrm{g})+\mathrm{H}_{2}(\mathrm{g})\) \(\Delta G^{\circ}=-28.6 \mathrm{kJ}\) Combine the preceding equations, as necessary, to obtain \(\Delta G^{\circ}\) values for the following reactions. (a) \(\operatorname{COS}(\mathrm{g})+2 \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \longrightarrow\) \(\begin{aligned} \mathrm{SO}_{2}(\mathrm{g})+\mathrm{CO}(\mathrm{g})+2 \mathrm{H}_{2}(\mathrm{g}) & \Delta G^{\circ}=? \end{aligned}\) (b) \(\cos (g)+3 \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \longrightarrow\) \(\mathrm{SO}_{2}(\mathrm{g})+\mathrm{CO}_{2}(\mathrm{g})+3 \mathrm{H}_{2}(\mathrm{g}) \quad \Delta G^{\circ}=?\) \(\left.+\quad \mathrm{H}_{\mathrm{O}} \mathrm{C}(\mathrm{d})=\mathrm{CO}_{-}^{\circ} \mathrm{G}\right)+\mathrm{H}_{-}^{-} \mathrm{S}(\mathrm{q})\) (c) \(\cos (\mathrm{g})+\mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \longrightarrow \mathrm{CO}_{2}(\mathrm{g})+\mathrm{H}_{2} \mathrm{S}(\mathrm{g})\) \(\Delta G^{\circ}=?\) Of reactions (a), (b), and (c), which is spontaneous in the forward direction when reactants and products are present in their standard states?

For the dissociation of \(\mathrm{CaCO}_{3}(\mathrm{s})\) at \(25^{\circ} \mathrm{C}, \mathrm{CaCO}_{3}(\mathrm{s})\) \(\rightleftharpoons \mathrm{CaO}(\mathrm{s})+\mathrm{CO}_{2}(\mathrm{g}) \Delta G^{\circ}=+131 \mathrm{kJ} \mathrm{mol}^{-1} .\) A sample of pure \(\mathrm{CaCO}_{3}(\mathrm{s})\) is placed in a flask and connected to an ultrahigh vacuum system capable of reducing the pressure to \(10^{-9} \mathrm{mmHg}\) (a) Would \(\mathrm{CO}_{2}(\mathrm{g})\) produced by the decomposition of \(\mathrm{CaCO}_{3}(\mathrm{s})\) at \(25^{\circ} \mathrm{C}\) be detectable in the vacuum system at \(25^{\circ} \mathrm{C} ?\) (b) What additional information do you need to determine \(P_{\mathrm{CO}_{2}}\) as a function of temperature? (c) With necessary data from Appendix D, determine the minimum temperature to which \(\mathrm{CaCO}_{3}(\mathrm{s})\) would have to be heated for \(\mathrm{CO}_{2}(\mathrm{g})\) to become detectable in the vacuum system.

Use thermodynamic data from Appendix D to calculate values of \(K_{\mathrm{sp}}\) for the following sparingly soluble solutes: (a) \(\operatorname{AgBr} ;\) (b) \(\operatorname{CaSO}_{4} ;\) (c) \(\operatorname{Fe}(\text { OH })_{3}\). [Hint: Begin by writing solubility equilibrium expressions.

Titanium is obtained by the reduction of \(\mathrm{TiCl}_{4}(1)\) which in turn is produced from the mineral rutile \(\left(\mathrm{TiO}_{2}\right)\) (a) With data from Appendix D, determine \(\Delta G^{\circ}\) at 298 K for this reaction. $$\mathrm{TiO}_{2}(\mathrm{s})+2 \mathrm{Cl}_{2}(\mathrm{g}) \longrightarrow \mathrm{TiCl}_{4}(1)+\mathrm{O}_{2}(\mathrm{g})$$ (b) Show that the conversion of \(\mathrm{TiO}_{2}(\mathrm{s})\) to \(\mathrm{TiCl}_{4}(1)\) with reactants and products in their standard states, is spontaneous at \(298 \mathrm{K}\) if the reaction in (a) is coupled with the reaction $$2 \mathrm{CO}(\mathrm{g})+\mathrm{O}_{2}(\mathrm{g}) \longrightarrow 2 \mathrm{CO}_{2}(\mathrm{g})$$

Arrange the entropy changes of the following processes, all at \(25^{\circ} \mathrm{C},\) in the expected order of increasing \(\Delta S,\) and explain your reasoning: (a) \(\mathrm{H}_{2} \mathrm{O}(1,1 \mathrm{atm}) \longrightarrow \mathrm{H}_{2} \mathrm{O}(\mathrm{g}, 1 \mathrm{atm})\) (b) \(\mathrm{CO}_{2}(\mathrm{s}, 1 \mathrm{atm}) \longrightarrow \mathrm{CO}_{2}(\mathrm{g}, 10 \mathrm{mm} \mathrm{Hg})\) (c) \(\mathrm{H}_{2} \mathrm{O}(1,1 \mathrm{atm}) \longrightarrow \mathrm{H}_{2} \mathrm{O}(\mathrm{g}, 10 \mathrm{mmHg})\)

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free