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Vikentia [17]
3 years ago
8

At a different temperature (this means that Keq will be different than part a)), 6.0 mol of IF5 and 8.0 mol of I4F2 are placed i

n a 10.0 L container. At equilibrium, 6.0mol of I4F2 are left. Calculate the Keq for the new temperature.
Chemistry
1 answer:
antoniya [11.8K]3 years ago
4 0

Answer:

Keq for the new temperature is 26.8

Explanation:

Let's propose the equilibrium:

2IF₅ +  I₄F₂  ⇄  3I₂  +  6F₂

Now we propose the situations:

                2IF₅     +      I₄F₂    ⇄    3I₂   +     6F₂

Initial      6 mol           8 mol           -              -

Initially we added 6 mol and 8 mol of our reactants  

React.        x                 x/2           3/2x         3x

By stoichiometry x amount has reacted, so a half of x react to the I₄F₂ and we finally produced 3/2x and 3x in the product side

Eq.          (6 - x)        (8 - x/2)        3/2x          3x

Notice we have the concentration left for the I₄F₂, so we can find the x value, the amount that has reacted:

8 - x/2 = 6

x = 4, so the concentrations in the equilibrium are:

2 moles of IF₅, 6 moles I₄F₂, 6 moles of I₂ and 12 moles of F₂

As we need molar concentration to determine Keq, we must divide the moles by the volume of the container:

2/10 = [IF₅] → 0.2 M

6/10 = [I₄F₂] → 0.6 M

6/10 = [I₂] → 0.6 M

12/10 = [F₂] → 1.2 M

Let's make, expression for Keq:

Keq = ([I₂]³ . [F₂]⁶) / [IF₅]² . [I₄F₂]

Keq = 0.6³ . 1.2⁶ / 0.2² . 0.6 → 26.8

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Answer:

41.3 s

Explanation:

Let t₁ represent the time taken for SO₂ to effuse.

Let t₂ represent the time taken for Ar to effuse.

Let M₁ represent the molar mass of SO₂

Let M₂ represent the molar mass of Ar

From the question given above,

Time taken (t₁) for SO₂ = 52.3 s

Time taken (t₂) for Ar =?

Molar mass (M₁) of SO₂ = 32 + (16×2) = 32 + 32 = 64 g/mol

Molar mass (M₂) of Ar = 40 g/mol

Finally, we shall determine the time taken for Ar to effuse by using the Graham's law equation as shown below:

t₂ / t₁ = √(M₂ / M₁)

t₂ / 52.3 = √(40 / 64)

t₂ / 52.3 = √0.625

t₂ / 52.3 = 0.79

Cross multiply

t₂ = 52.3 × 0.79

t₂ = 41.3 s

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Use the given data at 500 K to calculate ΔG°for the reaction
Anton [14]

Answer : The  value of \Delta G^o for the reaction is -959.1 kJ

Explanation :

The given balanced chemical reaction is,

2H_2S(g)+3O_2(g)\rightarrow 2H_2O(g)+2SO_2(g)

First we have to calculate the enthalpy of reaction (\Delta H^o).

\Delta H^o=H_f_{product}-H_f_{reactant}

\Delta H^o=[n_{H_2O}\times \Delta H_f^0_{(H_2O)}+n_{SO_2}\times \Delta H_f^0_{(SO_2)}]-[n_{H_2S}\times \Delta H_f^0_{(H_2S)}+n_{O_2}\times \Delta H_f^0_{(O_2)}]

where,

\Delta H^o = enthalpy of reaction = ?

n = number of moles

\Delta H_f^0 = standard enthalpy of formation

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

\Delta H^o=[2mole\times (-242kJ/mol)+2mole\times (-296.8kJ/mol)}]-[2mole\times (-21kJ/mol)+3mole\times (0kJ/mol)]

\Delta H^o=-1035.6kJ=-1035600J

conversion used : (1 kJ = 1000 J)

Now we have to calculate the entropy of reaction (\Delta S^o).

\Delta S^o=S_f_{product}-S_f_{reactant}

\Delta S^o=[n_{H_2O}\times \Delta S_f^0_{(H_2O)}+n_{SO_2}\times \Delta S_f^0_{(SO_2)}]-[n_{H_2S}\times \Delta S_f^0_{(H_2S)}+n_{O_2}\times \Delta S_f^0_{(O_2)}]

where,

\Delta S^o = entropy of reaction = ?

n = number of moles

\Delta S_f^0 = standard entropy of formation

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

\Delta S^o=[2mole\times (189J/K.mol)+2mole\times (248J/K.mol)}]-[2mole\times (206J/K.mol)+3mole\times (205J/K.mol)]

\Delta S^o=-153J/K

Now we have to calculate the Gibbs free energy of reaction (\Delta G^o).

As we know that,

\Delta G^o=\Delta H^o-T\Delta S^o

At room temperature, the temperature is 500 K.

\Delta G^o=(-1035600J)-(500K\times -153J/K)

\Delta G^o=-959100J=-959.1kJ

Therefore, the value of \Delta G^o for the reaction is -959.1 kJ

3 0
3 years ago
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