IB Chemistry HL Topic 5 — How Far? The Position of Equilibrium Paper 1 & 2 Core skill ~9 min read

The Equilibrium Law

The equilibrium law is the recipe for turning a balanced equation into an equilibrium constant expression. There is no thinking to do once you know the pattern — but there are three places students trip: which side goes on top, where the powers come from, and which species you leave out altogether.

📘 What you need to know

The pattern, once and for all

Write out the balanced equation. Put the products on top, the reactants on the bottom, and raise each concentration to the power of its balancing number. That is the whole law.

The equilibrium law For aA + bB ⇌ cC + dD:
K = [C]c[D]d[A]a[B]b
Turning a balanced equation into a K expression The four highlighted numbers are the only things that set the powers a A + b B c C + d D reactant side product side [C]c[D]d K = [A]a[B]b products go on top reactants go underneath each coefficient becomes a power Balance the equation before you write anything An unbalanced equation gives the wrong powers, so every later answer is wrong too.
The dashed lines are the only mapping you need to remember: the number in front of a species becomes the power on its square bracket.

🧩 Writing any K expression

  1. Balance the equation. Non-negotiable — the powers come from here.
  2. Cross out any solid, and any pure liquid. They never appear in the expression.
  3. Write the fraction line. Products above, reactants below.
  4. Copy each surviving species in square brackets, in the order it appears.
  5. Add the powers from the balancing numbers. A coefficient of 1 needs no power.

Which species get left out

This is the part the pattern alone will not tell you. A concentration only means something if the substance can spread out and get more or less crowded. A block of solid cannot: its “concentration” is fixed by its density, so it is folded into K and never written.

GOES IN THE EXPRESSION

  • Gases (g)
  • Dissolved species (aq)
  • Liquids that are part of a mixture, such as ethanol and ethanoic acid in an esterification

These can genuinely be more or less concentrated, so their concentration is a real variable.

LEFT OUT COMPLETELY

  • Solids (s)
  • Pure liquids on their own, such as water in H2O(l) ⇌ H2O(g)
  • Water as the solvent in a dilute aqueous reaction

Their concentration cannot change in any useful way, so it is absorbed into the value of K.

Quick sanity check: grinding a solid into powder or adding a bigger lump changes nothing about the equilibrium position. That is exactly why solids are missing from the expression.
Look at the state symbols before you write a single bracket. An equilibrium with an (s) in it is the classic trap — students dutifully include it and lose the mark on an otherwise perfect expression.

K belongs to one particular equation

There is no such thing as “the K of ammonia”. K is tied to the exact equation you wrote down, including which way round it is and what the coefficients are. Change the equation and K changes in a predictable way.

What you do to the equationWhat happens to KWhy, in one line
Reverse itK becomes 1 ÷ KTop and bottom of the fraction swap over
Double every coefficientK becomes K2Every power doubles, so the whole fraction is squared
Halve every coefficientK becomes √KEvery power halves, so you take the square root
Multiply every coefficient by nK becomes KnSame logic as doubling, generalised
Add two equations togetherK becomes K1 × K2The two fractions multiply, and the shared terms cancel

🧠 Remembering the reverse rule

Reversing the equation flips the fraction upside down, and flipping a fraction is the same as taking 1 over it. So a reaction with K = 100 going forwards has K = 0.01 going backwards. Big K one way always means tiny K the other way — a useful check on your answer.

Worked examples

WORKED EXAMPLE

Write the K expression for three reactions

(a) 2SO2(g) + O2(g) ⇌ 2SO3(g)
(b) CH4(g) + H2O(g) ⇌ CO(g) + 3H2(g)
(c) Cu(s) + 2Ag+(aq) ⇌ Cu2+(aq) + 2Ag(s)

(a) Everything is a gas, so nothing is left out K = [SO3]2[SO2]2[O2] O₂ has a coefficient of 1, so it gets no power (b) Watch the 3 in front of hydrogen K = [CO][H2]3[CH4][H2O] H₂O is a gas here, so it does count (c) Two solids to cross out first K = [Cu2+][Ag+]2 Cu(s) and Ag(s) never appear the 2 in front of Ag(s) is ignored too – it vanishes with the solid
WORKED EXAMPLE

A heterogeneous equilibrium

Ammonium chloride sublimes in a sealed tube: NH4Cl(s) ⇌ NH3(g) + HCl(g). Write the expression for K, and state what happens to the equilibrium if more solid NH4Cl is added at constant temperature.

Step 1: Cross out the solid NH₄Cl(s) is not included, so the bottom of the fraction is empty. Step 2: Write the products only K = [NH3][HCl] Step 3: Adding more solid The solid is not in the expression, so nothing in K can change. No shift — the gas concentrations stay exactly the same adding more solid just gives you more unreacted solid
WORKED EXAMPLE

Rewriting the equation, rewriting K

At 373 K, for N2O4(g) ⇌ 2NO2(g), K = 0.212. Calculate K at the same temperature for
(a) 2NO2(g) ⇌ N2O4(g) and (b) ½N2O4(g) ⇌ NO2(g).

(a) This is the reverse reaction, so take 1 over K K = 10.212 = 4.7169… K = 4.72 (3 s.f.) (b) Every coefficient has been halved, so square root it K = √0.212 = 0.46043… K = 0.460 (3 s.f.) check: 0.460 squared gives 0.212 back, so the direction of the change is right

💡 Exam tip

⚠ Common mix-up

Up next: The Equilibrium Constant, Kc — what the actual number tells you about how far a reaction goes, and how to calculate it from data.

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