136 End-of-Chapter Material

Exercises

1. Classify each of the following as spontaneous or nonspontaneous processes:

a)  the browning of a cut apple slice on a snack tray over time

b)  the rolling of a ball uphill

c)  the formation of diamond from the graphite in your pencil

d)  the melting of ice cubes in a glass of water you are holding

 

2. State the second law of thermodynamics.

 

3. What sign would you expect for ΔS for the following processes?

a)  water freezing in a lake during a cold Alberta winter

b)  AB(s) + CD(s) → AC(g) + BD(g)

c)  a balloon with a fixed amount of gas stretched to a larger volume

d)  the sublimation of dry ice

e)  3 E₂F₂(g) → E₆F₆(g)

 

4. Which of the following would you expect to have the higher standard molar entropy, S⁰?

a)  Br₂(ℓ) or Br₂(g)

b)  NO₂(g) or NO(g)

c)  C₂H₆(g) or C₅H₁₂(g)

 

5. Calculate the ΔS⁰ of the following reactions using the values listed in the appendix.

a)  4 NH₃(g) + 5 O₂(g) → 6 H₂O(g)  + 4 NO(g)

b)  2 HgO(s) → 2 Hg(ℓ)  + O₂(g)

c)  3 FeCl₂(s) + KNO₃(s) + 4 HCl (aq) → 3 FeCl₃(s) + KCl(s) + NO(g) + 2 H₂O(ℓ)

6. Draw a diagram showing the approximate entropy change of water from -100⁰C to 250⁰C.

 

7. A chemical reaction has ΔH⁰ = -43.5 kJ and ΔS⁰ = -65.8 J/K. Calculate ΔG⁰ at 298 K. Is this a spontaneous process?

 

8. Using data from the appendix, determine ΔG⁰ for all reactions listed in question 5.

 

9. Find the standard Gibbs energy change for the reaction

CaCO₃(s) → CaO(s) + CO₂(g)

The ΔG_f° values for the three components of this reaction system are CaCO₃(s): –1128 kJ mol^–1; CaO(s): –603.5 kJ/mol; CO₂(g): –137.2 kJ/mol.^[1]

 

10. Using the appendix data, determine the approximate temperature at which the following processes are at equilibrium:

a)  CH₂Cl₂(ℓ) → CH₂Cl₂(g)

b)  CH₃OH(ℓ) → CH₃OH(g)

 

11. Determine if the following reactions would be spontaneous at any temperature, nonspontaneous at any temperature, spontaneous at low temperature but not high temperature, or spontaneous at high temperature but not low temperature:

 

a)  ΔH⁰ = -750 kJ and ΔS⁰ = 250 J/K

b)  ΔH⁰ = -100 kJ and ΔS⁰ = -300 J/K

c)  ΔH⁰ = 95 kJ and ΔS⁰ = -70 J/K

d)  ΔH⁰ = 400 kJ and ΔS⁰ = 500 J/K

 

12. The K_a for acetic acid, CH₃COOH, is 1.75 x 10^-5 at 25⁰C.

a)  Using the K_a value, determine the ΔG⁰ for the dissociation of acetic acid in aqueous solution.

b)  What is the value of ΔG when [H⁺] is 7.5 x 10^-2 M, [CH₃COO^–] is 2.5 x 10^-2 M, and [CH₃COOH] is 0.10 M?

 

13. Calculate the equilibrium constant for the reaction H⁺(aq) + OH^–(aq) → H₂O(ℓ) from the following data:

	H+(aq)	OH–(aq)	H2(ℓ)
ΔH°f, kJ mol–1	0	–230.0	–285.8
S°, J K–1 mol–1	0*	–10.9	70.0

* Note that the standard entropy of the hydrogen ion is zero by definition. This reflects the fact that it is impossible to carry out thermodynamic studies on a single-charged species. All ionic entropies are relative to that of H⁺(aq), which explains why some values (as for the aqueous hydroxide ion) are negative.^[2]

 

14. Using data from the appendix, calculate the equilibrium constants at 298 K for all the reactions in question 5.

Answers

1.

a)  spontaneous

b) nonspontaneous

c)  nonspontaneous

d)  spontaneous

3.

a)  ΔS = –

b)  ΔS = +

c)  ΔS = +

d)  ΔS = +

e)  ΔS = –

5.

a)

ΔS⁰ = ∑nS⁰(products) – ∑mS⁰(reactants)

ΔS⁰ = (6 S⁰ H₂O(g)  + 4 S⁰ NO(g)) – (4 S⁰ NH₃(g)  + 5 S⁰ O₂(g))

ΔS⁰ = [(6 x 188.8 J/mol K) + (4 x 210.8 J/mol K)] – [(4 x 192.8 J/mol K) + (5 x 205.2 J/mol K)]

ΔS⁰ = 178.8 J/mol K

b)

ΔS⁰ = ∑nS⁰(products) – ∑mS⁰(reactants)

ΔS⁰ = (2 S⁰ Hg(ℓ) + S⁰ O₂(g)) – (2 S⁰ HgO)

ΔS⁰ = [(2 x 75.9 J/mol K) + (205.2 J/mol K)] – (2 x 70.3 J/mol K)

ΔS⁰ = 216.4 J/mol K

c)

ΔS⁰ = ∑nS⁰(products) – ∑mS⁰(reactants)

ΔS⁰ = (3 S⁰ FeCl₃(s) + S⁰ KCl(s) + S⁰ NO(g) + 2 S⁰ H₂O(ℓ))- (3 S⁰ FeCl₂(s) + S⁰ KNO₃(s) + 4 S⁰ HCl (aq))

ΔS⁰ = [(3 x 142.3 J/mol K) + (82.6 J/mol K) + (210.8 J/mol K) + (2 x 70.0 J/mol K)] – [(3 x 118.0 J/mol K) + (133.1 J/mol K) + (4 x 56.5 J/mol K)]

ΔS⁰ = 147.2 J/mol K

7.

ΔG⁰ = ΔH⁰ – TΔS⁰

ΔG⁰ = -43.5 kJ – [(298 K)(-65.8 J/K)]

ΔG⁰ = -23.9 kJ

ΔG⁰ is negative therefore this is a spontaneous process.

9.

ΔG° = (–603.5 –137.2) – (–1128) kJ/mol = +130.9 kJ/mol, indicating that the process is not spontaneous under standard conditions (i.e., solid calcium carbonate will not form solid calcium oxide and CO₂ at 1 atm partial pressure at 25°C.)

11.

a)  spontaneous at all temperatures

b)  spontaneous at low temperatures, nonspontaneous at high temperatures

c)  nonspontaneous at all temperatures

d)  spontaneous at high temperatures, nonspontaneous at low temperatures

13.

ΔH° = (∑ΔH°_f, products) – (∑ΔH°_f, reactants) = (–285.8) – (–230) = –55.8 kJ/mol

ΔS° = (∑ΔS°, products) – (∑ΔS°, reactants) = (70.0) – (–10.9) = +80.8 J/mol K

The value of ΔG° at 298 K is ΔH° – TΔS° = (–55,800) – (298)(80.8) = –79,900 J/mol

K = exp(–79,900/(8.314 × 298) = e^-32.2 = 1.01 × 10^-14