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Determine the standard enthalpy change, entropy change, and free energy change for the conversion of diamond to graphite. Discuss the spontaneity of the conversion with respect to the enthalpy and entropy changes. Explain why diamond spontaneously changing into graphite is not observed.

Short Answer

Expert verified
  • The change of enthalpy is \(\Delta H = - 1.89\frac{{kJ}}{{mol}}\)
  • The change of entropy is \(\Delta S = 3.36\frac{J}{{K \cdot mol}}\)
  • The change of free energy is \(\Delta G = - 2.90\frac{{kJ}}{{mol}}\)
  • The reaction is spontaneous. It is normally observed because the rate of the reaction is very slow.

Step by step solution

01

Definition of Gibbs free energy

Gibbs free energy, also known as Gibbs function, Gibbs energy, or free enthalpy, is a term used to measure the topmost quantum of work done in a thermodynamic system when temperature and pressure remain constant.

02

Determine the Change of entropy and enthalpy.

The reaction in question is:

\(C({\rm{ diamond }}) \to C(graphite)\)

We can calculate the enthalpy change using the formula

\(\Delta H = {H_f}({\rm{ products }}) - {H_f}({\rm{ reactants }})\)

We can look up the standard formation enthalpy changes in the table in AppendixG in the book.

\(\Delta H = {H_f}(C,{\rm{ graphite }}) - {H_f}(C,{\rm{ diamond }})\)

\(\begin{array}{l}\Delta H = (0 - 1.89)\frac{{k \cdot J}}{{mol}}\\\Delta H = - 1.89\frac{{kJ}}{{mol}}\end{array}\)

Hence, the change of enthalpy is \(\Delta H = - 1.89\frac{{kJ}}{{mol}}\)

We can calculate the entropy change using the formula

\(\Delta S = S({\rm{ products }}) - S({\rm{ reactants }})\)

We can look up the standard entropies in the table in AppendixG in the book.

\(\begin{array}{l}\Delta S = S(C,{\rm{ graphite }}) - S(C,{\rm{ diamond }})\\\Delta S = (5.740 - 2.38)\frac{J}{{K \cdot mol}}\\\Delta S = 3.36\frac{J}{{K \cdot mol}}\end{array}\)

Hence, the change of entropy is \(\Delta S = 3.36\frac{J}{{K \cdot mol}}\)

03

Determine the Change of free energy.

If we look at the formula for \(\Delta G\) :

\(\Delta G = \Delta H - T\Delta S\)

We can see that, if the enthalpy change is negative and the entropy change is positive, such as the case is with this reaction, \(\Delta G\) will surely be negative and the reaction therefore spontaneous. We can calculate the free energy change using the formula

\(\Delta G = {G_f}({\rm{ products }}) - {G_f}({\rm{ reactants }})\)

We can look up the standard formation free energy changes for each species in AppendixG in the book.

\(\begin{array}{l}\Delta G = {G_f}(C,{\rm{ graphite }}) - {G_f}(C,{\rm{ diamond }})\\\Delta G = (0 - 2.90)\frac{{k \cdot J}}{{mol}}\\\Delta G = - 2.90\frac{{kJ}}{{mol}}\end{array}\)

Even though the conversion of diamond to graphite is a spontaneous reaction, it is not normally observed because the rate of the reaction is very slow.

Hence, the change of free energy is \(\Delta G = - 2.90\frac{{kJ}}{{mol}}\)

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Most popular questions from this chapter

Predict the sign of the enthalpy change for the following processes. Give a reason for your prediction.

(a) \({\bf{NaN}}{{\bf{O}}_{\bf{3}}}{\bf{(s)}} \to {\bf{N}}{{\bf{a}}^{\bf{ + }}}{\bf{(aq) + N}}{{\bf{O}}_{\bf{3}}}^{\bf{ - }}{\bf{(aq)}}\)

(b) the freezing of liquid water

(c) \({\bf{C}}{{\bf{O}}_{\bf{2}}}{\bf{(s)}} \to {\bf{C}}{{\bf{O}}_{\bf{2}}}{\bf{(g)}}\)

(d) \({\bf{CaCO(s)}} \to {\bf{CaO(s) + C}}{{\bf{O}}_{\bf{2}}}{\bf{(g)}}\)

Use the information in Appendix G to estimate the boiling point of CS2.

Balance the following reactions and write the reactions using cell notation. Ignore any inert electrodes, as they are never part of the half-reactions.

(a) \({\rm{Al}}(s) + {\rm{Z}}{{\rm{r}}^{4 + }}(aq) \to {\rm{A}}{{\rm{l}}^{3 + }}(aq) + {\rm{Zr}}(s)\)

(b) \({\rm{A}}{{\rm{g}}^ + }(aq) + {\rm{NO}}(g) \to {\rm{Ag}}(s) + {\rm{N}}{{\rm{O}}_3}^ - (aq)\)(acidic solution)

(c) \({\rm{Si}}{{\rm{O}}_3}^{2 - }(aq) + {\rm{Mg}}(s) \to {\rm{Si}}(s) + {\rm{Mg}}{({\rm{OH}})_2}(s)\)(basic solution)

(d) \({\rm{Cl}}{{\rm{O}}_3}^ - (aq) + {\rm{Mn}}{{\rm{O}}_2}(s) \to {\rm{C}}{{\rm{l}}^ - }(aq) + {\rm{Mn}}{{\rm{O}}_4}^ - (aq)\)(basic solution

"Thermite" reactions have been used for welding metal parts such as railway rails and in metal refining. One such thermite reaction is \({\bf{F}}{{\bf{e}}_{\bf{2}}}{{\bf{O}}_{\bf{3}}}{\bf{(s) + 2Al(s)}} \to {\bf{A}}{{\bf{l}}_{\bf{2}}}{{\bf{O}}_{\bf{3}}}{\bf{(s) + 2Fe(s)}}\). Is the reaction spontaneous at room temperature under standard conditions? During the reaction, the surroundings absorb \({\bf{851}}{\bf{.8\;kJ/mol}}\)of heat.

When ammonium chloride is added to water and stirred, it dissolves spontaneously and the resulting solution feels cold. Without doing any calculations, deduce the signs of \(\Delta G,{\rm{ }}\Delta H\), and \(\Delta S\) for this process, and justify your choices.

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