TutorChase logo
Login

IBDP Chemistry HL Cheat Sheet - Reactivity 2.3 - How far? The extent of chemical change

Dynamic equilibrium

  • Dynamic equilibrium is reached in a closed system when the rate of the forward reaction = rate of the backward reaction.

  • At equilibrium, concentrations/macroscopic properties stay constant, but particles are still reacting.

  • Applies to both physical equilibrium and chemical equilibrium.

  • In exam wording, constant concentration does not mean the reaction has stopped.

Pasted image

This figure shows dynamic equilibrium: particles continue changing in both directions, but the overall amounts remain constant because the forward and reverse rates are equal. It is a useful visual reminder that equilibrium is dynamic, not static. Source

Equilibrium constant, KK

  • The equilibrium law gives an expression for KK from the stoichiometric coefficients in the balanced equation.

  • For a general homogeneous reaction, aA+bBcC+dDaA + bB \rightleftharpoons cC + dD:

    • K=[C]c[D]d[A]a[B]bK = \dfrac{[C]^c[D]^d}{[A]^a[B]^b}

  • Products go on top, reactants on the bottom.

  • Each concentration is raised to the power of its coefficient.

  • In this topic, you must be able to deduce the equilibrium expression from the equation.

  • For IB exam technique: write the balanced equation first, then build the KK expression carefully from coefficients.

What the size of KK means

  • The magnitude of KK shows the extent of reaction at equilibrium.

  • K1K \ll 1 → equilibrium lies far to the left; mostly reactants.

  • K<1K < 1reactants favored.

  • K=1K = 1appreciable amounts of both reactants and products.

  • K>1K > 1products favored.

  • K1K \gg 1 → equilibrium lies far to the right; mostly products.

  • KK is temperature dependent.

  • For the reverse reaction at the same temperature: Kreverse=1KforwardK_{\text{reverse}} = \dfrac{1}{K_{\text{forward}}}.

Le Châtelier’s principle

  • Le Châtelier’s principle predicts how an equilibrium system responds to a stress.

  • The system shifts to oppose the change and re-establish equilibrium.

  • You must apply this to changes in concentration, pressure, and temperature.

Pasted image

These diagrams summarize how equilibrium shifts when concentration, pressure, or temperature changes. They are helpful for building a fast decision process in exam questions. Source

Changing concentration

  • Increasing a reactant shifts equilibrium to the right.

  • Increasing a product shifts equilibrium to the left.

  • Removing a reactant shifts equilibrium to the left.

  • Removing a product shifts equilibrium to the right.

  • KK does not change when only concentration changes.

  • The equilibrium composition changes, but the value of KK stays the same.

Changing pressure

  • Pressure changes matter only when gases are involved.

  • Increasing pressure favors the side with fewer moles of gas.

  • Decreasing pressure favors the side with more moles of gas.

  • If both sides have the same total moles of gas, changing pressure causes no shift.

  • KK does not change when only pressure changes.

  • Always compare gaseous moles only; ignore solids and liquids.

Changing temperature

  • Treat heat as a reactant or product.

  • For an endothermic forward reaction, increasing temperature shifts equilibrium to the right.

  • For an exothermic forward reaction, increasing temperature shifts equilibrium to the left.

  • Temperature change is the one common stress that changes the value of KK.

  • If the forward reaction is endothermic, increasing temperature increases KK.

  • If the forward reaction is exothermic, increasing temperature decreases KK.

Catalysts and equilibrium

  • A catalyst speeds up both the forward and backward reactions.

  • A catalyst helps the system reach equilibrium faster.

  • A catalyst does not change the value of KK.

  • A catalyst does not change the equilibrium composition.

Heterogeneous equilibria

  • Le Châtelier’s principle can also be applied to heterogeneous equilibria, for example: X(g)X(aq)X(g) \rightleftharpoons X(aq)

  • Focus on how changing conditions affects the position of equilibrium.

  • In equilibrium expressions, remember that in many cases pure solids and pure liquids are omitted.

Checklist: can you do this?

  • State the conditions required for dynamic equilibrium.

  • Write a correct equilibrium expression from a balanced homogeneous equation.

  • Interpret the size of KK to describe whether reactants or products are favored.

  • Predict the shift caused by a change in concentration, pressure, or temperature.

  • Distinguish between changes that affect equilibrium composition and changes that affect the value of KK.

HL only – Reaction quotient, QQ

  • The reaction quotient, QQ, uses the same form as the equilibrium expression but with non-equilibrium concentrations.

  • Compare QQ with KK to predict the direction of change:

    • Q=KQ = K → system is at equilibrium.

    • Q<KQ < K → reaction proceeds forward to make more products.

    • Q>KQ > K → reaction proceeds backward to make more reactants.

  • This is a high-value exam skill for determining the direction the mixture will shift before equilibrium is reached.

HL only – Solving equilibrium problems

  • You must solve problems using KK together with initial and equilibrium concentrations.

  • A common method is an ICE table:

    • I = initial concentrations

    • C = change

    • E = equilibrium concentrations

  • Use the stoichiometric ratios to write the change terms.

  • Substitute equilibrium values into the KK expression.

  • In this syllabus, quadratic equations are not expected.

  • Only homogeneous equilibria are assessed quantitatively here.

HL only – Gibbs energy and equilibrium

  • ΔG\Delta G^\circ and KK both describe the position of equilibrium.

  • Use: ΔG=RTlnK\Delta G^\circ = -RT\ln K

  • Meanings to know:

    • ΔG<0\Delta G^\circ < 0K>1K > 1, so products are favored.

    • ΔG>0\Delta G^\circ > 0K<1K < 1, so reactants are favored.

    • ΔG=0\Delta G^\circ = 0K=1K = 1.

  • In calculations, use Kelvin for temperature.

  • Watch units carefully when using RR and ΔG\Delta G^\circ.

Exam traps to avoid

  • Do not say equilibrium means equal concentrations; it means equal rates.

  • Do not include substances incorrectly in a KK or QQ expression.

  • Do not say a catalyst shifts equilibrium; it only makes equilibrium faster to reach.

  • Do not confuse changing concentration/pressure with changing KK; only temperature changes KK.

  • Do not forget that KK for the reverse reaction is the reciprocal of the forward reaction.

Fast exam summary

  • Equilibrium = closed system, forward rate = backward rate, constant macroscopic quantities.

  • Large KK means products favored; small KK means reactants favored.

  • Concentration and pressure can change the position of equilibrium, but not KK.

  • Temperature changes both the position of equilibrium and KK.

  • HL: use QQ, ICE tables, and ΔG=RTlnK\Delta G^\circ = -RT\ln K to quantify equilibrium.

Dr Shubhi Khandelwal avatar
Written by:
Dr Shubhi Khandelwal
Qualified Dentist and Expert Science Educator

Shubhi is a seasoned educational specialist with a sharp focus on IB, A-level, GCSE, AP, and MCAT sciences. With 6+ years of expertise, she excels in advanced curriculum guidance and creating precise educational resources, ensuring expert instruction and deep student comprehension of complex science concepts.

Hire a tutor

Please fill out the form and we'll find a tutor for you.

1/2
Your details
Alternatively contact us via
WhatsApp, Phone Call, or Email