IB Chemistry SL Topic 5 — The Extent of Chemical Change Paper 1 & 2 Core idea ~14 min read

Le Chatelier’s Principle

You know where a reaction settles. Now the useful part: how to move it somewhere better. One sentence covers every case, and the whole skill is learning to apply it without waving your hands.

📚 What you need to know

Position of equilibrium

The phrase “position of equilibrium” just means the relative amounts of reactants and products in the mixture. A shift to the right means more product and less reactant; a shift to the left means the reverse.

Le Chatelier’s principle if a change is made to a system at equilibrium,
the position of equilibrium moves to minimise that change
The word to hold on to is oppose. The system is not trying to help you, and it does not restore things completely — it pushes back against whatever you did and settles somewhere new. Every prediction in this topic is the same two-step thought: what did I change, and which direction partly undoes it?

Changing a concentration

Add more of a reactant and, for a moment, the ratio of products to reactants is too small to be the equilibrium value. Collisions between reactant particles become more frequent, the forward reaction speeds up, and product builds until the original ratio is restored. That restored ratio is K, unchanged.

THE SYSTEM MOVES AWAY FROM WHATEVER YOU ADDA + B ⇌ C + DADD MORE Atoo much reactant presentshifts RIGHTusing the extra A upREMOVE C AS IT FORMSnot enough product presentshifts RIGHTreplacing what you tookADD MORE Ctoo much product presentshifts LEFTremoving the extra Cthe shift always partly undoes the change you madepartly, never completely — opposed is not the same as cancelled
Continuously removing a product is the industrial chemist’s favourite trick: the equilibrium keeps shifting right and never gets the chance to settle.
Diluting an aqueous equilibrium with water looks like a concentration change, but if there are the same number of aqueous species on each side it dilutes everything equally, the ratio is untouched, and nothing shifts. Count the species before you answer.

Changing the pressure

Pressure only matters where gases are involved, because only gases are compressible enough for it to make any difference. Squeeze a gas mixture into a smaller volume and every concentration rises; the system responds by reducing the total number of gas molecules, which lowers the pressure again.

PRESSURE COUNTS MOLECULES OF GASN₂O₄(g) ⇌ 2NO₂(g)1 molecule of gas2 molecules of gasincrease the pressuredecrease the pressureequal numbers of gas molecules on each side, or no gases at all, means no shift
Count only the gas molecules. Solids and solutions are left out of the count entirely, so a solid on one side does not tip the balance.
Do not go looking for a “high pressure side” and a “low pressure side”. Compare the number of moles of gas written on each side of the equation, and that is the whole calculation. If they are the same, pressure changes nothing at all — a favourite one-mark question.

Changing the temperature

Heating a system supplies energy. The equilibrium opposes that by shifting in whichever direction absorbs energy, which is the endothermic one. Cooling does the opposite: the exothermic direction is favoured because it releases energy to replace what you removed.

HEATING ALWAYS FAVOURS THE ENDOTHERMIC DIRECTIONFORWARD REACTION IS EXOTHERMICA + B ⇌ CΔH is negative going rightheat it → shifts LEFTcool it → shifts RIGHTa better yield in the cold, but slowerFORWARD REACTION IS ENDOTHERMICA + B ⇌ CΔH is positive going rightheat it → shifts RIGHTcool it → shifts LEFTyield and rate both improve on heatingtemperature is the only change here that alters the value of K
Check the sign of ΔH for the forward reaction first, then decide which way is endothermic. Everything else follows from that one reading.

Temperature is also the only change that alters K itself. Look at what happens to an endothermic reaction on heating: the products increase and the reactants decrease, so the numerator of the expression grows while the denominator shrinks, and the value of K must rise. For an exothermic reaction the same reasoning gives a fall.

Catalysts

A catalyst speeds up the forward and reverse reactions by the same factor. The two rates therefore become equal at exactly the same composition as before — the system simply gets there sooner.

A catalyst has no effect on the position of equilibrium and no effect on K. It cannot improve a yield. Writing that a catalyst increases the amount of product is one of the quickest ways to lose a mark in this topic.

Everything on one page

ChangeWhich way does the equilibrium shift?Value of K
Increase concentration of a reactantright, to use it upunchanged
Decrease concentration of a reactantleft, to replace itunchanged
Increase concentration of a productleft, to use it upunchanged
Remove a product as it formsright, to replace itunchanged
Increase pressure (decrease volume)towards fewer gas moleculesunchanged
Decrease pressure (increase volume)towards more gas moleculesunchanged
Increase temperaturein the endothermic directionchanges
Decrease temperaturein the exothermic directionchanges
Add a catalystno shift — equilibrium is reached fasterunchanged

🧩 Answering any Le Chatelier question

  1. Name the change. Concentration, pressure, temperature or catalyst?
  2. Find the relevant feature. Which species changed, how many gas molecules on each side, or what is the sign of ΔH.
  3. State the direction of the shift, left or right.
  4. Justify it by saying what the shift opposes.
  5. Say what would be observed, or what happens to the yield, if the question asks.
WORKED EXAMPLE

N2O4 is colourless and NO2 is dark brown. For N2O4(g) ⇌ 2NO2(g), ΔH = +57 kJ mol–1. State and explain the colour change observed when the sealed tube is (a) placed in iced water, (b) compressed to half its volume.

(a) cooling the tube The forward reaction is endothermic, so the reverse reaction is exothermic. Cooling favours the exothermic direction. shifts left, the colour fades Less NO₂ and more colourless N₂O₄. K also falls, because this is a temperature change. (b) halving the volume There is 1 mol of gas on the left and 2 mol on the right, so the equilibrium shifts left to reduce the pressure. shifts left, but the colour deepens The catch: squashing the gas concentrates everything first, so the tube darkens immediately, then pales a little as the equilibrium shifts. The final colour is still darker than at the start. K is unchanged.
WORKED EXAMPLE

For the Contact process, 2SO2(g) + O2(g) ⇌ 2SO3(g), ΔH = –196 kJ mol–1. State the conditions that would give the highest possible yield, and explain why the temperature actually used is far higher.

Temperature for maximum yield The forward reaction is exothermic, so a low temperature shifts the equilibrium right. as low as possible Pressure for maximum yield 3 mol of gas on the left, 2 mol on the right, so a high pressure shifts the equilibrium right. high pressure Why the real temperature is high At a low temperature the reaction is far too slow to be useful, and the catalyst works poorly. A moderate temperature of roughly 450 °C sacrifices some yield to gain an acceptable rate. a compromise between yield and rate In practice the yield is already very high near atmospheric pressure, so plants do not pay for high pressure equipment. Good chemistry is not always the answer with the best K.
WORKED EXAMPLE

Predict, with a reason, the effect of each change.
(a) Adding water to the equilibrium Ce4+(aq) + Fe2+(aq) ⇌ Ce3+(aq) + Fe3+(aq)
(b) Adding a catalyst to N2(g) + 3H2(g) ⇌ 2NH3(g)
(c) Increasing the pressure on H2(g) + I2(g) ⇌ 2HI(g)

(a) diluting the ions no shift Two aqueous species on each side, so the water dilutes both sides equally and the ratio is unchanged. (b) adding a catalyst no shift, no change in yield Both rates increase by the same factor, so equilibrium is reached sooner at exactly the same composition. (c) raising the pressure no shift 2 mol of gas on the left and 2 mol on the right. All three concentrations rise, and the expression is unaffected because the powers balance.

Equilibria that are not all in one phase

The principle applies just as well when the phases differ. A sealed bottle of fizzy drink holds an equilibrium between dissolved and gaseous carbon dioxide, at a pressure well above atmospheric.

In the bottle CO2(g) ⇌ CO2(aq)

Open the cap and gaseous carbon dioxide escapes, so its pressure drops sharply. The equilibrium shifts to replace it, dissolved gas comes out of solution, and you see the bubbles. Leave the bottle open long enough and the drink goes flat — the system has become open, so it runs to completion rather than settling.

💡 Exam tip

⚠️ Common mix-up

Up next: Measuring Reaction Rates — how far a reaction goes is only half the question. The compromise conditions in the Contact process only make sense once you can talk properly about the other half: how fast.

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