7.1: chemical equilibria: reversible reactions, dynamic equilibrium

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24 Terms

1
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Define a reversible reaction

A reaction in which products can be turned back into reactants by reversing conditions

2
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In dynamic equilibrium:

The rate of the forwards and backwards reaction is the same in a closed system

The concentrations of the reactants and products are constant

3
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When does the concentration stop changing in a reaction?

When equilibrium is reached

4
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What does Le Chatelier’s principle state?

if a change is made to a system at dynamic equilibrium, the position of the equilibrium moves to minimise this change

5
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If the concentration of a reactant is increased:

Equilibrium shifts to the right

6
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If the concentration of a product is increased

Equilibrium shifts to left

7
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If pressure is increased:

Equilibrium shifts in the direction that produces a smaller number of molecules of gas to decrease the pressure again

8
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If temperature is increased

  • Equilibrium moves in the endothermic direction to reverse the change

9
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If temperature is decreased

  • Equilibrium moves in the exothermic direction to oppose the change 

10
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Explain the effect of catalysts

  • Substance that increases the rate of a chemical reaction

  • Increase the rate of the forward and reverse reaction equally

  • Only cause a reaction to reach its equilibrium faster

  • Catalysts therefore have no effect on the position of the equilibrium once this is reached

11
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What is Kc defined as

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12
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Which state is ignored in Kc expressions?

Solids

13
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Define partial pressure

The pressure exerted by particular gas A in a mixture of gases

14
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Mole fraction=

The number of moles of a particular gas/ total number of moles of all gases in a mixture

15
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Partial pressure =

Mole fraction x total pressure

16
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What is the only factor that can change Kc?

Temperature

17
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Explain how ammonia yield is maximised in the haber process in terms of pressure

  • Increasing pressure shifts equilibrium to the right, increasing ammonia yield

  • Higher pressure also increases collision frequency, enhancing the reaction rate

  • However, very high pressures are costly and require strong containment

  • Compromise pressure used

    • ≈ 200 atm

18
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Explain how ammonia yield is maximised in the haber process in terms of temperature

  • The forward reaction is exothermic

  • Lowering temperature shifts equilibrium to the right, favouring ammonia formation

  • But too low a temperature would slow the reaction rate, delaying equilibrium

  • Compromise temperature:

    • 400–450 °C

19
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Explain how ammonia yield is maximised in the haber process in terms of removing ammonia

  • Ammonia is removed by cooling and condensing it to a liquid

  • This shifts the equilibrium further to the right, producing more ammonia

  • Stored ammonia is kept at low temperatures where decomposition is very slow, especially in the absence of a catalyst

20
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Explain how ammonia yield is maximised in the haber process in terms of using a catalyst

  • An iron catalyst is used to increase the rate of reaction without affecting equilibrium position

  • Without it, the reaction would be too slow


21
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Explain how ammonia yield is maximised in the contact process in terms of pressure

  • Increasing pressure shifts equilibrium to the right, favouring SO3 formation

  • However, the equilibrium constant (Kp) is already very large at low pressures

  • Industrial pressure used:

    • ~1 atm

22
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Explain how ammonia yield is maximised in the contact process in terms of temperature

  • Reaction is exothermic

  • Lower temperatures would favour SO3 production, but also reduce the rate

  • Compromise temperature:

    • ≈ 450 °C

23
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Explain how ammonia yield is maximised in the contact process in terms of removing sulfuric acid

Shifts equilibrium to the right, driving reaction forward

24
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Explain how ammonia yield is maximised in the contact process in terms of using a catalyst

Contact process uses vanadium(V) oxide as a catalyst to increase the rate of reaction