Reversible Reactions

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Reversible Reactions,
Chemical Equilibrium,
Ammonia - its synthesis and
uses
1. Reversible Reactions
 A reversible reaction is a chemical in which the products can be converted back to reactants
under suitable conditions.
 A reversible reaction is shown by the sign a half-arrow to the right (forward

reaction) and a half-arrow to the left (backward reaction).
 Most reactions are not reversible and have the usual complete arrow only pointing to
the right.
Three examples of reversible reactions are given below:
(a) The thermal decomposition of ammonium chloride.
 On heating strongly, the white solid ammonium chloride, decomposes into a mixture of two
colourless gases ammonia and hydrogen chloride.
 On cooling the reaction is reversed and solid ammonium chloride reforms.
o This is an example of sublimation but involving both physical and chemical
changes.
o Ammonium chloride + heat ammonia + hydrogen chloride
o NH4Cl(s) NH3(g) + HCl(g)

 Note:
o Reversing the reaction conditions reverses the direction of chemical change, typical
of a reversible reaction.
o Thermal decomposition means using 'heat' to 'break down' a molecule into smaller
ones.
o The decomposition is endothermic (heat absorbed or heat taken in) and the
formation of ammonium chloride is exothermic (heat released or heat given out).
o This means if the direction of chemical change is reversed, the energy change is
also reversed.
(b) The thermal decomposition of hydrated copper(II) sulphate.
 On heating the blue solid, hydrated copper(II) sulphate, steam is given off and the white
solid of anhydrous copper(II) sulphate is formed.
 When the white solid is cooled and water added, blue hydrated copper(II) sulphate is
reformed.
blue hydrated copper(II) sulphate + heat white anhydrous copper(II) sulphate +

water
CuSO4.5H2O(s) CuSO4(s) + 5H2O(g)
Note:
 The 5H2O in the formula of hydrated copper(II) sulphate is called the water of
crystallisation and forms part of the crystal structure when copper(II) sulphate solution is
evaporated and crystals form.
 This crystal structure is broken down on heating and the water is given off.
 The thermal decomposition is endothermic as heat is absorbed to drive off the water.
 The reverse reaction is exothermic ie on adding water to white anhydrous copper(II)
sulphate the mixture heats up as the blue crystals reform.
 The reverse reaction is used as a simple chemical test for water ie white anhydrous
copper(II) sulphate turns blue.
2. Reversible reactions and Equilibrium.
Reversible reactions and equilibrium
A reversible reaction is one in which the products of a reaction can react back to
produce the original reactants. The reaction can go both ways:
H2(g) + I2(g) <=> 2HI(g)

hydrogen combines with iodine in hydrogen iodide molecules react to form
<=>
the forward reaction hydrogen and iodine in the reverse reaction
If the reaction is carried out in a closed container, a point is reached where the
concentration of products and reactants does not change. We say that an
equilibrium (balance) has been reached.
The amounts of reactants and products present at equilibrium depend on the

temperature, pressure and concentration of reactants at the start.
If we remove the products from an equilibrium reaction more reactants are

2
converted to products.
For an exothermic equilibrium reaction, the amount of product decreases as the

temperature increases. For an endothermic equilibrium reaction, the amount of
product increases as the temperature increases.
Equation Effect of increasing pressure

N2(g) + 3H2(g) 2NH3(g) 2 More ammonia is formed. Increasing the pressure
<=>
4 molecules molecules pushes the reaction in the direction of fewer molecules.
N2O4(g) 1 2NO2(g) 2 More N2O4(g) is formed. Increasing the pressure
<=>
molecule molecules pushes the reaction in the direction of fewer molecules.
H2(g) + I2(g) 2 2HI(g) 2 No effect, because there are the same number of
<=>
molecules molecules molecules on each side of the equation.
 When a reversible reaction occurs in a closed system an equilibrium is formed, in which
the original reactants and products formed coexist.
 In an equilibrium there is a state of balance between the concentrations of the reactants
and products.
 At equilibrium the rate at which the reactants change into products is exactly equal to the
rate at which the products change back to the original reactants.
 The result is that that the concentrations of the reactants and products remain the same
BUT the reactions don't stop!
 However the relative amounts of the reactants and products depend on the reaction
conditions eg the temperature and pressure.
 For industrial processes, it is important to maximise the concentration of the desired
products and minimise the 'leftover' reactants. A set of rules can be used to predict the best
reaction conditions to give the highest possible yield of product.
Rule 1a: If the forward reaction forming the product is endothermic, raising the temperature
favours its formation increasing the yield of product (lowering the temperature decreases the
yield).
Rule 1b: If the forward reaction forming the product is exothermic, decreasing the temperature
favours its formation (increasing temperature decreases the yield).
Rule 1 applies to any reaction BUT rule 2 applies to a reaction with one or gaseous reactants or
products.
Rule 2a: Increasing the pressure favours the side of the equilibrium with the least number
of gaseous molecules as shown by the balanced symbol equation.
Rule 2b: Decreasing the pressure favours the side of the equilibrium with the most number of
3
gaseous molecules as shown by the balanced symbol equation
Rule 3a: If the concentration of a reactant (on the left) is increased, then some of it must change
to the products (on the right) to maintain a balanced equilibrium position.
Rule 3b: If the concentration of a reactant (on the left) is decreased, then some of the products
(on the right) must change back to reactants to maintain a balanced equilibrium position.
 eg nitrogen + hydrogen ammonia or N2(g) + 3H2(g) 2NH3(g)

o if the nitrogen or hydrogen concentration was increased, some of this extra gas
concentration would change to ammonia
o if the nitrogen or hydrogen concentration was decreased, some of ammonia would
change to nitrogen and ammonia
 increasing nitrogen => decreases hydrogen and increases ammonia
 increasing hydrogen => decreases nitrogen and increases ammonia
 increasing ammonia => increases nitrogen and hydrogen
 decreasing ammonia => decreases nitrogen and hydrogen
 decreasing nitrogen ==> increases hydrogen and decreases
ammonia
 decreasing hydrogen ==> increases nitrogen and decreases
ammonia
Rule 4: A catalyst does NOT affect the position of an equilibrium, you just get there faster!
A catalyst usually speeds up both the forward and reverse reaction but there is no way it can
influence the final 'balanced' concentrations. However, the importance of a catalyst lies with
economics eg (i) bringing about reactions with high activation energies at lower temperatures and
so saving energy or (ii) saving time is saving money.
(a) The formation of calcium oxide (lime) and carbon dioxide from
calcium carbonate (limestone)
CaCO3(s) CaO(s) + CO2(g)
The forward reaction is endothermic, 178kJ of heat energy is absorbed (taken in) for every mole of
calcium oxide formed.
One mole of gas is formed in the process, so there is a net increase in the moles of gas in lime
formation, since there are no gaseous reactants.
From rule 1: increasing the temperature will increase the yield of lime CaO (endothermic).
From rule 2: decreasing the pressure will favour the formation of more carbon dioxide, hence more
lime (increase in gas molecules).
Lime is made commercially by heating limestone to a high temperature (eg 1000 oC) in a limekiln
that is well ventilated (this reduces the carbon dioxide pressure and so reduces the un-desired
backward reaction).
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(b) The formation of hydrogen chloride from hydrogen and chlorine
H2(g) + Cl2(g) 2HCl(g)
The forward reaction is exothermic, 184kJ of heat energy is given out in forming hydrogen chloride
(92 kJ per mole of HCl formed).
There is no net change in the moles of gas (2 moles reactants 2 moles of product)
From rule 1: decreasing the temperature favours the formation of hydrogen chloride HCl
From rule 2: since there is no net change in the moles of gas, pressure has no effect on the yield of
hydrogen chloride!
3. The Synthesis of ammonia - The Haber Process

 Ammonia gas is synthesised in the chemical industry by reacting nitrogen gas with
hydrogen gas.
 The nitrogen is obtained from air (80% of air is N2).
 The hydrogen is made by reacting methane (natural gas) and water or from
cracking hydrocarbons (both reactions are done at high temperature with a catalyst).
o CH4 + H2O ==> 3H2 + CO
o eg C8H18 ==> C8H16 + H2
 The synthesis equation for this reversible reaction is ...
N2(g) + 3H2(g) 2NH3(g)
 .. which means a dynamic equilibrium will form, so no chance of 100% yield!

 In forming ammonia 92kJ of heat energy is given out (ie exothermic, 46kJ of heat
released per mole of ammonia formed).
 Four moles of 'reactant' gas form two moles of 'product' gas, so there is net decrease in gas
molecules on forming ammonia.
 So applying the equilibrium rules from section 2 the formation of ammonia is favoured by
o using high pressure because you are going from 4 to 2 gas molecules (the high
pressure also speeds up the reaction because it effectively increases the
concentration of the gas molecules).
o and low temperature because is an exothermic reaction,
o to try to get the optimum conditions to get the biggest yield of ammonia,
o these arguments make the point that the yield* of an equilibrium reaction
depends on the conditions used.
 * The word 'yield' means how much product you get compared to
the theoretical maximum possible if the reaction goes 100%.
 In industry pressures of 200 - 300 times normal atmospheric pressure are used in
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line with the theory.
 Theoretically a low temperature would give a high yield of ammonia BUT ...
o Nitrogen is very stable molecule and not very reactive ie chemically inert.
o To speed up the reaction an iron catalyst is used as well as a higher
temperature (eg 400-450oC).
o The higher temperature is an economic compromise, ie it is more economic to get a
low yield fast, than a high yield slowly!
o Note: a catalyst does NOT affect the yield of a reaction, ie the equilibrium
position BUT you do get there faster!
 On cooling the reacted mixture the ammonia liquefies and is removed and stored in
cylinders.
 Any unreacted nitrogen or hydrogen is recycled back through the reactor chamber,
nothing is wasted!
DONE

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 A reversible reaction is shown by the sign a half-arrow to the right (forward

Three examples of reversible reactions are given below:

(a) The thermal decomposition of ammonium chloride.

o Ammonium chloride + heat ammonia + hydrogen chloride

o NH4Cl(s) NH3(g) + HCl(g)

blue hydrated copper(II) sulphate + heat white anhydrous copper(II) sulphate +

CuSO4.5H2O(s) CuSO4(s) + 5H2O(g)

2. Reversible reactions and Equilibrium.

Reversible reactions and equilibrium

H2(g) + I2(g) <=> 2HI(g)

The amounts of reactants and products present at equilibrium depend on the

If we remove the products from an equilibrium reaction more reactants are

For an exothermic equilibrium reaction, the amount of product decreases as the

Equation Effect of increasing pressure

 eg nitrogen + hydrogen ammonia or N2(g) + 3H2(g) 2NH3(g)

CaCO3(s) CaO(s) + CO2(g)

H2(g) + Cl2(g) 2HCl(g)

3. The Synthesis of ammonia - The Haber Process

N2(g) + 3H2(g) 2NH3(g)

 .. which means a dynamic equilibrium will form, so no chance of 100% yield!

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