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Popular chemical hand warmers generate heat by the air-oxidation of iron:\({\bf{4Fe(s) + 3}}{{\bf{O}}_{\bf{2}}}{\bf{(g)}} \to {\bf{2F}}{{\bf{e}}_{\bf{2}}}{{\bf{O}}_{\bf{3}}}{\bf{(s)}}\).How does the spontaneity of this process depend upon temperature?

Short Answer

Expert verified

The given reaction is non-spontaneous at higher temperatures and more spontaneous at lower temperatures.

Step by step solution

01

Define enthalpy of the reaction

The change in Gibbs free energy is as follows:

\({\bf{\Delta G = \Delta H - T\Delta S}}\)

where,

\({\bf{\Delta G }}\) = the change in Gibbs free energy,

\({\bf{\Delta H}}\)= the change in enthalpy,

T = the absolute temperature in Kelvin and

\({\bf{\Delta S}}\)= the change in entropy.

The Gibbs free energy change is used to determine the spontaneity of a process. It is expressed in terms of the enthalpy and the entropy of a system.

02

Determine the Gibbs free energy change using free energies of formation  

The air-oxidation reaction of iron generates heat. The reaction is as follows:

\(4{\rm{Fe}}({\rm{s}}) + 3{{\rm{O}}_2}(\;{\rm{g}}) \to 2{\rm{F}}{{\rm{e}}_2}{{\rm{O}}_3}(\;{\rm{s}})\)

The spontaneity of a reaction is dependent upon the Gibbs free energy change, whereas free energy change depends on the temperature, change in enthalpy and change in entropy. According to Le Chatelier's Principle, when the temperature is increased in an exothermic reaction, the equilibrium moves in the backward direction, thereby resulting in less spontaneity in the forward direction. When the temperature is decreased, the equilibrium moves in the forward direction, and the reaction is also more spontaneous.

03

Determine the Gibbs free energy change using entropies

The reaction of air-oxidation of iron is as follows:

\(4{\rm{Fe}}({\rm{s}}) + 3{{\rm{O}}_2}(\;{\rm{g}}) \to 2{\rm{F}}{{\rm{e}}_2}{{\rm{O}}_3}(\;{\rm{s}})\)

Heat is released during the air-oxidation of iron; hence it is an exothermic reaction. For the exothermic reaction, the value of change in enthalpy is negative. For the reaction to be spontaneous, the value of change in free energy should also be negative.

04

Determine the Gibbs free energy change using free energies of formation  

\(\Delta {\rm{G}} = \Delta {\rm{H}} - {\rm{T}}\Delta {\rm{S}}\)

For spontaneous reaction,

\(\begin{array}{l}\Delta {\rm{G}} = {\rm{ negative }}\\\Delta {\rm{H}} = {\rm{ negative}}\end{array}\)

The value of change in free energy will be negative only when the value of \(T\)∆\(S\) is less than ∆\({\rm{H}}\). Hence, the given reaction is non-spontaneous at higher temperatures and more spontaneous at lower temperatures.

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Most popular questions from this chapter

Calculate ΔG° using

(a) free energies of formation and

(b) enthalpies of formation and entropies(Appendix G). Do the results indicate the reaction to be spontaneous or nonspontaneous at 25 °C?

\({{\bf{C}}_{\bf{2}}}{{\bf{H}}_{\bf{4}}}{\bf{(g)}} \to {{\bf{H}}_{\bf{2}}}{\bf{(g) + }}{{\bf{C}}_{\bf{2}}}{{\bf{H}}_{\bf{4}}}{\bf{(g)}}\)

Carbon tetrachloride, an important industrial solvent, is prepared by the chlorination of methane at \(850\;{\rm{K}}\).

\({\rm{C}}{{\rm{H}}_4}(g) + 4{\rm{C}}{{\rm{l}}_2}(g) \to {\rm{CC}}{{\rm{l}}_4}(g) + 4{\rm{HCl}}(g)\)

What is the equilibrium constant for the reaction at \(850\;{\rm{K}}\)? Would the reaction vessel need to be heated or cooled to keep the temperature of the reaction constant?

What happens to \({\bf{\Delta G}}_{{\bf{298}}}^{\bf{^\circ }}\) (becomes more negative or more positive) for the following chemical reactions when the partial pressure of oxygen is increased?

(a) \({\bf{S(s) + }}{{\bf{O}}_{\bf{2}}}{\bf{(g)}} \to {\bf{S}}{{\bf{O}}_{\bf{2}}}{\bf{(g)}}\)

(b) \({\bf{2S}}{{\bf{O}}_{\bf{2}}}{\bf{(g) + }}{{\bf{O}}_{\bf{2}}}{\bf{(g)}} \to {\bf{S}}{{\bf{O}}_{\bf{3}}}{\bf{(g)}}\)

(c) \({\bf{HgO(s)}} \to {\bf{Hg(l) + }}{{\bf{O}}_{\bf{2}}}{\bf{(g)}}\)

Describe how matter and/or energy is redistributed when you empty a canister of compressed air into a room.

Although the gas used in the oxyacetylene torch Figure (5.7) is essentially pure acetylene, the heat produced by the combustion of one mole ofacetylene in such a torch is likely, not equal to the enthalpy of combustion of acetylene listed in the table 5.2. Considering the conditions for which the tabulated data are reported. Suggest an explanation.

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