The fuel in high-efficiency natural gas vehicles consists primarily of methane \(\left(\mathrm{CH}_{4}\right) .\) (a) How much heat is produced in burning 1 mol of \(\mathrm{CH}_{4}(g)\) under standard conditions if reactants and products are brought to \(298 \mathrm{~K}\) and \(\mathrm{H}_{2} \mathrm{O}(l)\) is formed? (b) What is the maximum amount of useful work that can be accomplished under standard conditions by this system?

Short Answer

Expert verified
The heat produced in burning 1 mol of CH4(g) is 965.1 kJ/mol, and the maximum amount of useful work that can be accomplished under standard conditions by this system is 884.3 kJ/mol.

Step by step solution

01

Determine the balanced chemical equation for the combustion of CH4

Using the formula for the combustion of a hydrocarbon, we can find the balanced chemical equation for the combustion of CH4: CH4 (g) + 2 O2 (g) -> CO2 (g) + 2 H2O (l)
02

Find the standard enthalpy change of the reaction

We can calculate the standard enthalpy change of the reaction (∆H°) as follows: ∆H° = [n * ∆H°f(products)] - [n * ∆H°f(reactants)] Standard enthalpy of formation (∆H°f) values for the compounds are as follows: ∆H°f(CH4 (g)) = -74.8 kJ/mol ∆H°f(O2 (g)) = 0 kJ/mol (since it's an element in its standard state) ∆H°f(CO2 (g)) = -393.5 kJ/mol ∆H°f(H2O (l)) = -285.8 kJ/mol Now, we can calculate ∆H° for the reaction: ∆H° = [1(-393.5) + 2(-285.8)] - [1(-74.8) + 2(0)] ∆H° = (-393.5 - 2 * 285.8) - (-74.8) ∆H° = -965.1 kJ/mol The heat produced in burning 1 mol of CH4(g) is 965.1 kJ/mol.
03

Calculate the standard Gibbs free energy change of the reaction

Now we need to find the standard Gibbs free energy change of the reaction (∆G°) to determine the maximum amount of useful work that can be accomplished under standard conditions. We can do this by using the following equation: ∆G° = ∆H° - T∆S° First, we need to find the standard entropy change (∆S°) for the reaction: ∆S° = [n * S°(products)] - [n * S°(reactants)] Standard molar entropy (S°) values for the compounds are as follows: S°(CH4 (g)) = 186.3 J/mol·K S°(O2 (g)) = 205.2 J/mol·K S°(CO2 (g)) = 213.8 J/mol·K S°(H2O (l)) = 69.9 J/mol·K Now, we can calculate ∆S° for the reaction: ∆S° = [1(213.8) + 2(69.9)] - [1(186.3) + 2(205.2)] ∆S° = (213.8 + 2 * 69.9) - (186.3 + 410.4) ∆S° = -270.8 J/mol·K Now we can calculate the ∆G° for the reaction at 298 K: ∆G° = ∆H° - T∆S° ∆G° = -965.1 kJ/mol - (298 K)(-270.8 J/mol·K) / 1000 (to convert J to kJ) ∆G° = -965.1 kJ/mol + 80.8 kJ/mol ∆G° = -884.3 kJ/mol The maximum amount of useful work that can be accomplished under standard conditions by this system is 884.3 kJ/mol.

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Most popular questions from this chapter

For the majority of the compounds listed in Appendix \(\mathrm{C},\) the value of \(\Delta G_{f}^{\circ}\) is more positive (or less negative) than the value of \(\Delta H_{f}^{\circ} .\) (a) Explain this observation, using \(\mathrm{NH}_{3}(g), \mathrm{CCl}_{4}(l)\), and \(\mathrm{KNO}_{3}(s)\) as examples. (b) An exception to this observation is \(\mathrm{CO}(g)\). Explain the trend in the \(\Delta H_{f}^{\circ}\) and \(\Delta G_{f}^{\circ}\) values for this molecule.

Consider a process in which an ideal gas changes from state 1 to state 2 in such a way that its temperature changes from \(300 \mathrm{~K}\) to \(200 \mathrm{~K}\). (a) Describe how this change might be carried out while keeping the volume of the gas constant. (b) Describe how it might be carried out while keeping the pressure of the gas constant. (c) Does the change in \(\Delta E\) depend on the particular pathway taken to carry out this change of state? Explain.

Consider the following equilibrium: $$ \mathrm{N}_{2} \mathrm{O}_{4}(g) \rightleftharpoons 2 \mathrm{NO}_{2}(g) $$ Thermodynamic data on these gases are given in Appendix C. You may assume that \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) do not vary with temperature. (a) At what temperature will an equilibrium mixture contain equal amounts of the two gases? (b) At what temperature will an equilibrium mixture of 1 atm total pressure contain twice as much \(\mathrm{NO}_{2}\) as \(\mathrm{N}_{2} \mathrm{O}_{4} ?\) (c) At what temperature will an equilibrium mixture of 10 atm total pressure contain twice as much \(\mathrm{NO}_{2}\) as \(\mathrm{N}_{2} \mathrm{O}_{4} ?\) (d) Rationalize the results from parts (b) and (c) by using Le Châtelier's principle. [Section 15.7]

(a) Give two examples of endothermic processes that are spontaneous. (b) Give an example of a process that is spontaneous at one temperature but nonspontaneous at a different temperature.

The crystalline hydrate \(\mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2} \cdot 4 \mathrm{H}_{2} \mathrm{O}(s)\) loses water when placed in a large, closed, dry vessel: $$ \mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2} \cdot 4 \mathrm{H}_{2} \mathrm{O}(s) \longrightarrow \mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2}(s)+4 \mathrm{H}_{2} \mathrm{O}(g) $$ This process is spontaneous and \(\Delta H\) is positive. Is this process an exception to Bertholet's generalization that all spontaneous changes are exothermic? Explain.

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