Sulfuric acid is produced in larger amounts by weight than any other chemical. It is used in manufacturing fertilizers, oil refining, and hundreds of other processes. An intermediate step in the industrial process for the synthesis of H2SO4 is the catalytic oxidation of sulfur dioxide: 2SO2(g)+O2(g)→2SO3(g)ΔG∘ = -141.8 kJ Calculate ΔG at 25 ∘C given the following sets of partial pressures.Part A
130atm SO2, 130atm O2, 2.0atm SO3
Express your answer using four significant figures.
Part B
5.0atm SO2, 3.0atm O2, 30atm SO3
Express your answer using four significant figures.
Part CEach reactant and product at a partial pressure of 1.0 atm.
Express your answer using four significant figures.

Respuesta :

Answer:

A. -166.6 kJ/mol

B. -127.7 kJ/mol

C. -133.9 kJ/mol

Explanation:

Let's consider the oxidation of sulfur dioxide.

2 SO₂(g) + O₂(g) → 2 SO₃(g)     ΔG° = -141.8 kJ

The Gibbs free energy (ΔG) can be calculated using the following expression:

ΔG = ΔG° + R.T.lnQ

where,

ΔG° is the standard Gibbs free energy

R is the ideal gas constant

T is the absolute temperature (25 + 273.15 = 298.15 K)

Q is the reaction quotient

The molar concentration of each gas ([]) can be calculated from its pressure (P) using the following expression:

[tex][]=\frac{P}{R.T}[/tex]

Calculate ΔG at 25°C given the following sets of partial pressures.

Part A  130atm SO₂, 130atm O₂, 2.0atm SO₃. Express your answer using four significant figures.

[tex][SO_{2}]=[O_{2}]=\frac{130atm}{(0.08206atm.L/mol.K).298K} =5.32M[/tex]

[tex][SO_{3}]=\frac{2.0atm}{(0.08206atm.L/mol.K).298K} =0.0818M[/tex]

[tex]Q=\frac{[SO_3]^{2} }{[SO_{2}]^{2}.[O_{2}] } =\frac{0.0818^{2} }{5.32^{3} } =4.44 \times 10^{-5}[/tex]

ΔG = ΔG° + R.T.lnQ = -141.8 kJ/mol + (8.314 × 10⁻³ kJ/mol.K) × 298 K × ln (4.44 × 10⁻⁵) = -166.6 kJ/mol

Part B  5.0atm SO₂, 3.0atm O₂, 30atm SO₃  Express your answer using four significant figures.

[tex][SO_{2}]=\frac{5.0atm}{(0.08206atm.L/mol.K).298K}=0.204M[/tex]

[tex][O_{2}]=\frac{3.0atm}{(0.08206atm.L/mol.K).298K}=0.123M[/tex]

[tex][SO_{3}]=\frac{30atm}{(0.08206atm.L/mol.K).298K}=1.23M[/tex]

[tex]Q=\frac{[SO_3]^{2} }{[SO_{2}]^{2}.[O_{2}] } =\frac{1.23^{2} }{0.204^{2}.0.123 } =296[/tex]

ΔG = ΔG° + R.T.lnQ = -141.8 kJ/mol + (8.314 × 10⁻³ kJ/mol.K) × 298 K × ln 296 = -127.7 kJ/mol

Part C Each reactant and product at a partial pressure of 1.0 atm.  Express your answer using four significant figures.

[tex][SO_{2}]=[O_{2}]=[SO_{3}]=\frac{1.0atm}{(0.08206atm.L/mol.K).298K}=0.0409M[/tex]

[tex]Q=\frac{[SO_3]^{2} }{[SO_{2}]^{2}.[O_{2}] } =\frac{0.0409^{2} }{0.0409^{3}} =24.4[/tex]

ΔG = ΔG° + R.T.lnQ = -141.8 kJ/mol + (8.314 × 10⁻³ kJ/mol.K) × 298 K × ln 24.4 = -133.9 kJ/mol

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