Consider the decomposition of a metal oxide to its elements, where M represents a generic metal. M 3 O 4 ( s ) − ⇀ ↽ − 3 M ( s ) + 2 O 2 ( g ) What is the standard change in Gibbs energy for the reaction, as written, in the forward direction? Δ G ∘ rxn = kJ/mol What is the equilibrium constant of this reaction, as written, in the forward direction at 298 K? K = What is the equilibrium pressure of O2(g) over M(s) at 298 K?

Respuesta :

This is an incomplete question, here is a complete question.

Consider the decomposition of a metal oxide to its elements, where M represents a generic metal.

[tex]M_3O_4(s)\rightleftharpoons 3M(s)+2O_2(g)[/tex]

Substance      ΔG°f (kJ/mol)

M₃O₄                 -9.50

M(s)                       0

O₂(g)                     0

What is the standard change in Gibbs energy for the reaction, as written, in the forward direction? delta G°rxn = kJ / mol.

What is the equilibrium constant of this reaction, as written, in the forward direction at 298 K?

What is the equilibrium pressure of O₂(g) over M(s) at 298 K?

Answer :

The Gibbs energy of reaction is, 9.50 kJ/mol

The equilibrium constant of this reaction is, 0.0216

The equilibrium pressure of O₂(g) is, 0.147 atm

Explanation :

The given chemical reaction is:

[tex]PCl_3(l)\rightarrow PCl_3(g)[/tex]

First we have to calculate the Gibbs energy of reaction [tex](\Delta G^o)[/tex].

[tex]\Delta G^o=G_f_{product}-G_f_{reactant}[/tex]

[tex]\Delta G^o=[n_{M(s)}\times \Delta G^0_{(M(s))}+n_{O_2(g)}\times \Delta G^0_{(O_2(g))}]-[n_{M_3O_4(s)}\times \Delta G^0_{(M_3O_4(s))}][/tex]

where,

[tex]\Delta G^o[/tex] = Gibbs energy of reaction = ?

n = number of moles

Now put all the given values in this expression, we get:

[tex]\Delta G^o=[3mole\times (0kJ/mol)+2mole\times (0kJ/mol)]-[1mole\times (-9.50kJ/K.mol)][/tex]

[tex]\Delta G^o=9.50kJ/mol[/tex]

The Gibbs energy of reaction is, 9.50 kJ/mol

Now we have to calculate the equilibrium constant of this reaction.

The relation between the equilibrium constant and standard Gibbs free energy is:

[tex]\Delta G^o=-RT\times \ln K[/tex]

where,

[tex]\Delta G^o[/tex] = standard Gibbs free energy  = 9.50kJ/mol = 9500 J/mol

R = gas constant = 8.314 J/K.mol

T = temperature = 298 K

K  = equilibrium constant = ?

[tex]9500J/mol=-(8.314J/K.mol)\times (298K)\times \ln (K)[/tex]

[tex]K=0.0216[/tex]

The equilibrium constant of this reaction is, 0.0216

Now we have to calculate the equilibrium pressure of O₂(g).

The expression of equilibrium constant is:

[tex]K=(P_{O_2})^2[/tex]

[tex]0.0216=(P_{O_2})^2[/tex]

[tex]P_{O_2}=0.147atm[/tex]

The equilibrium pressure of O₂(g) is, 0.147 atm

The free energy change of the reaction is  9.40 kJ/mol. The equilibrium constant is  0.0225. The partial pressure of oxygen is 0.15 atm.

The equation is represented as follows;

M3O4 ( s ) ⇄ 3M ( s ) + 2O2 ( g )

The enthalpy change of the reaction is obtained using the relation;

ΔG∘rxn =  ΔGf∘products -  ΔGf∘reactants

ΔG∘rxn =[0 kJ/mol- 0kJ/mol] - (-9.40 kJ/mol)

ΔG∘rxn = 9.40 kJ/mol

Now;

ΔG∘ = -RTlnK

lnK = -ΔG∘/RT

K = e^-ΔG∘/RT

K = e^-(9.40 × 10^3J/mol/8.314 J/Kmol × 298 K)

K = 0.0225

Now;

K =(pO2)^2

pO2 = √K

pO2 =√ 0.0225

pO2 = 0.15 atm

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