Consider the reaction $2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g)$ (a) Using data from Appendix \(\mathrm{C},\) calculate \(\Delta G^{\circ}\) at \(298 \mathrm{~K}\). (b) Calculate \(\Delta G\) at \(298 \mathrm{~K}\) if the partial pressures of all gases are \(33.4 \mathrm{kPa}\).

Short Answer

Expert verified
(a) The standard Gibbs free energy change (∆G°) at 298 K is -171.2 kJ/mol. (b) The non-standard Gibbs free energy change (∆G) at 298 K with the given partial pressures is -142627.28 J/mol, which is approximately -142.63 kJ/mol.

Step by step solution

01

Calculate standard Gibbs free energy change

Using the ∆G° value for each species provided in Appendix C, we can calculate the standard Gibbs free energy change for the reaction. We have the reaction: 2 NO(g) + O₂(g) ⟶ 2 NO₂(g) Using the formula mentioned above, we get: ∆G° = Σ(ν_product * ∆G°_product) - Σ(ν_reactant * ∆G°_reactant) ∆G° = (2 * ∆G°(NO₂) - (2 * ∆G°(NO) + ∆G°(O₂)) Plug in the values for each species: ∆G° = (2 * 51.3 kJ/mol) - (2 * 86.6 kJ/mol + 0 kJ/mol) Calculate the Gibbs free energy change: ∆G° = -171.2 kJ/mol
02

Calculate reaction quotient

We are given that the partial pressures of all gases are 33.4 kPa. Calculate the reaction quotient Q using the partial pressures: Q = [NO₂]² / ([NO]² * [O₂]) Since the partial pressures are the same for each gas (33.4 kPa), we can write: Q = (33.4)² / ((33.4)² * 33.4) Q = 1 / 33.4
03

Calculate non-standard Gibbs Free Energy Change

Now, we can calculate the non-standard Gibbs free energy change (∆G) using the Van't Hoff equation: ∆G = ∆G° + RT ln(Q) Plug in the values: ∆G = -171.2 kJ/mol + (8.314 J/mol*K * 298 K * ln(1/33.4)) Don't forget to convert kJ to J: ∆G = -171200 J/mol + (8.314 J/mol*K * 298 K * ln(1/33.4)) Calculate the value to obtain the final answer: ∆G = -142627.28 J/mol In conclusion, (a) The standard Gibbs free energy change (∆G°) at 298 K is -171.2 kJ/mol. (b) The non-standard Gibbs free energy change (∆G) at 298 K with the given partial pressures is -142627.28 J/mol, which is approximately -142.63 kJ/mol.

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Most popular questions from this chapter

The conversion of natural gas, which is mostly methane, into products that contain two or more carbon atoms, such as ethane $\left(\mathrm{C}_{2} \mathrm{H}_{6}\right)$, is a very important industrial chemical process. In principle, methane can be converted into ethane and hydrogen: $$ 2 \mathrm{CH}_{4}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{6}(g)+\mathrm{H}_{2}(g) $$ In practice, this reaction is carried out in the presence of oxygen: $$ 2 \mathrm{CH}_{4}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{6}(g)+\mathrm{H}_{2} \mathrm{O}(g) $$ (a) Using the data in Appendix \(C\), calculate \(K\) for these reactions at \(25^{\circ} \mathrm{C}\) and \(500^{\circ} \mathrm{C}\). (b) Is the difference in \(\Delta G^{\circ}\) for the two reactions due primarily to the enthalpy term \((\Delta H)\) or the entropy term \((-T \Delta S)\) ? (c) Explain how the preceding reactions are an example of driving a nonspontaneous reaction, as discussed in the "Chemistry and Life" box in Section 19.7. (d) The reaction of \(\mathrm{CH}_{4}\) and \(\mathrm{O}_{2}\) to form \(\mathrm{C}_{2} \mathrm{H}_{6}\) and \(\mathrm{H}_{2} \mathrm{O}\) must be carried out carefully to avoid a competing reaction. What is the most likely competing reaction?

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. \((\mathbf{c})\) What is the "driving force" for the expansion of the gas: enthalpy or entropy?

The oxidation of glucose $\left(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}\right)\( in body tissue produces \)\mathrm{CO}_{2}$ and \(\mathrm{H}_{2} \mathrm{O} .\) In contrast, anaerobic decomposition, which occurs during fermentation, produces ethanol $\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\( and \)\mathrm{CO}_{2}$. (a) Using data given in Appendix \(\mathrm{C}\), compare the equilibrium constants for the following reactions: $$ \begin{array}{r} \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s)+6 \mathrm{O}_{2}(g) \rightleftharpoons 6 \mathrm{CO}_{2}(g)+6 \mathrm{H}_{2} \mathrm{O}(l) \\ \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s) \rightleftharpoons 2 \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(I)+2 \mathrm{CO}_{2}(g) \end{array} $$ (b) Compare the maximum work that can be obtained from these processes under standard conditions.

(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. (b) Use a reference source, such as Web Elements (www.webelements.com), to find the experimental melting and boiling points of \(I_{2}\). (c) Which of the values in part (b) is closer to the value you obtained in part (a)?

Sulfur dioxide reacts with strontium oxide as follows: $$ \mathrm{SO}_{2}(g)+\mathrm{SrO}(g) \longrightarrow \mathrm{SrSO}_{3}(s) $$ (a) Without using thermochemical data, predict whether \(\Delta G^{\circ}\) for this reaction is more negative or less negative than \(\Delta H^{\circ} .\) (b) If you had only standard enthalpy data for this reaction, how would you estimate the value of \(\Delta G^{\circ}\) at \(298 \mathrm{~K},\) using data from Appendix \(\mathrm{C}\) on other substances.

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