Octane \(\left(\mathrm{C}_{8} \mathrm{H}_{18}\right)\) is a liquid hydrocarbon at room temperature that is a constituent of gasoline. (a) Write a balanced equation for the combustion of \(\mathrm{C}_{8} \mathrm{H}_{18}(l)\) to form \(\mathrm{CO}_{2}(g)\) and \(\mathrm{H}_{2} \mathrm{O}(l) .\) (b) Without using thermochemical data, predict whether \(\Delta G^{\circ}\) for this reaction is more negative or less negative than \(\Delta H^{\circ} .\)

Short Answer

Expert verified
The balanced equation for the combustion of octane is: \(C_8H_{18}(l) + 12.5 \space O_2(g) \rightarrow 8 \space CO_2(g) + 9 \space H_2O(l)\). For this combustion reaction, the standard Gibbs Free Energy change (∆G°) is more negative than the standard Enthalpy change (∆H°) because it is highly exothermic and produces more gas molecules, resulting in a positive entropy change (∆S°).

Step by step solution

01

(a) Writing a balanced equation

To write a balanced equation for the combustion of octane, first, write the general equation: C8H18(l) + O2(g) → CO2(g) + H2O(l) Now, balance the equation: - Balance carbon atoms: There are 8 carbon atoms in C8H18, so 8 CO2 molecules are needed on the product side. - Balance hydrogen atoms: There are 18 hydrogen atoms in C8H18, so 9 H2O molecules are needed on the product side. - Finally, balance oxygen atoms: There are 16 oxygen atoms in 8 CO2 and 9 oxygen atoms in 9 H2O, adding up to 25 oxygen atoms on the right side. Since O2 has two oxygen atoms, we need 25/2, or 12.5, O2 molecules. The balanced equation is: \(C_8H_{18}(l) + 12.5 \space O_2(g) \rightarrow 8 \space CO_2(g) + 9 \space H_2O(l)\)
02

(b) Predicting the relationship between ∆G° and ∆H°

To predict the relationship between the standard Gibbs Free Energy change (∆G°) and the standard Enthalpy change (∆H°) for this reaction, consider the equation: \(\Delta G^\circ = \Delta H^\circ - T \Delta S^\circ\) For a combustion reaction, which is highly exothermic, the ∆H° value will be largely negative. The reaction also leads to an increase in entropy (∆S°) as the number of gas molecules in the products is higher than in the reactants (8 CO2 gas molecules formed and only 12.5 O2 gas molecules consumed). Thus, the ∆S° value will be positive. Because the temperature (T) is always positive, a positive ∆S° leads to a negative T∆S° term, which implies that the Gibbs Free Energy change (∆G°) would be more negative than the Enthalpy change (∆H°).

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Most popular questions from this chapter

Predict the sign of \(\Delta S_{\text { sys }}\) for each of the following processes: (a) Molten gold solidifies. (b) Gaseous \(C l_{2}\) dissociates in the stratosphere to form gaseous Cl atoms. (c) Gaseous CO reacts with gaseous \(\mathrm{H}_{2}\) to form liquid methanol, \(\mathrm{CH}_{3} \mathrm{OH} .(\mathbf{d})\) Calcium phosphate precipitates upon mixing \(\mathrm{Ca}\left(\mathrm{NO}_{3}\right)_{2}(a q)\) and \(\left(\mathrm{NH}_{4}\right)_{3} \mathrm{PO}_{4}(a q)\)

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) What is the "driving force" for the expansion of the gas: enthalpy or entropy?

Indicate whether each of the following statements is true or false. If it is false, correct it. (a) The feasibility of manufacturing \(\mathrm{NH}_{3}\) from \(\mathrm{N}_{2}\) and \(\mathrm{H}_{2}\) depends entirely on the value of \(\Delta H\) for the process \(\mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g)\) (b) The reaction of \(\mathrm{Na}(s)\) with \(\mathrm{Cl}_{2}(g)\) to form \(\mathrm{NaCl}(s)\) is a spontaneous process.(c) A spontaneous process can in principle be conducted reversibly. (d) Spontaneous processes in general require that work be done to force them to proceed. (e) Spontaneous processes are those that are exothermic and that lead to a higher degree of order in the system.

Indicate whether each statement is true or false. (a) A reaction that is spontaneous in one direction will be nonspontaneous in the reverse direction under the same reaction conditions. (b) All spontaneous processes are fast. (c) Most spontaneous processes are reversible. (d) An isothermal process is one in which the system loses no heat. (e) The maximum amount of work can be accomplished by an irreversible process rather than a reversible one.

Using the data in Appendix \(C\) and given the pressures listed, calculate \(K_{p}\) and \(\Delta G\) for each of the following reactions: $$ \begin{array}{l}{\text { (a) } \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g)} \\ {P_{\mathrm{N}_{2}}=2.6 \mathrm{atm}, P_{\mathrm{H}_{2}}=5.9 \mathrm{atm}, R_{\mathrm{NH}_{3}}=1.2 \mathrm{atm}} \\ {\text { (b) } 2 \mathrm{N}_{2} \mathrm{H}_{4}(g)+2 \mathrm{NO}_{2}(g) \longrightarrow 3 \mathrm{N}_{2}(g)+4 \mathrm{H}_{2} \mathrm{O}(g)} \\ {P_{\mathrm{N}_{2} \mathrm{H}_{4}}=P_{\mathrm{NO}_{2}}=5.0 \times 10^{-2} \mathrm{atm}} \\ {P_{\mathrm{N}_{2}}=0.5 \mathrm{atm}, P_{\mathrm{H}_{2} \mathrm{O}}=0.3 \mathrm{atm}}\\\\{\text { (c) }{\mathrm{N}_{2} \mathrm{H}_{4}(g) \longrightarrow \mathrm{N}_{2}(g)+2 \mathrm{H}_{2}(g)}} \\ {P_{\mathrm{N}_{2} \mathrm{H}_{4}}=0.5 \mathrm{atm}, P_{\mathrm{N}_{2}}=1.5 \mathrm{atm}, P_{\mathrm{H}_{2}}=2.5 \mathrm{atm}}\end{array} $$

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