2.3.5 (HL)—Reaction quotient (Q)

Syllabus
First assessment 2025
Objective
2.3.5
Level
HL

The Reaction Quotient Q

HL only

Q=productoverreactantconcentrationexpressionusingcurrentconcentrationsQ = product-over-reactant concentration expression using current concentrations

Q uses concentrations at any time, not necessarily equilibrium. Q < K means the forward direction is needed; Q > K means the reverse direction is needed; Q = K means equilibrium.

Calculate Q with the same expression as K but using the current concentrations. If Q = 0.20 and K = 5.0, too little product is present relative to equilibrium, so the forward direction lowers the mismatch. Recalculate after composition changes; Q is a snapshot, not a new constant.

Worked QQ example: for NX2(g)+3HX2(g)2NHX3(g)\ce{N2(g) + 3H2(g) <=> 2NH3(g)}, Q=[NHX3]2/([NX2][HX2]3)Q=[\ce{NH3}]^2/([\ce{N2}][\ce{H2}]^3). If every current concentration is 0.50moldm30.50\,\mathrm{mol\,dm^{-3}}, Q=(0.50)2/[(0.50)(0.50)3]=4.0Q=(0.50)^2/[(0.50)(0.50)^3]=4.0. At 475 K, K=0.59K=0.59, so Q>KQ>K: the mixture contains too much product relative to equilibrium and the reverse direction is favoured until Q=KQ=K.

Comparing Q with K

HL only

Assessment in practice

Representative question

Question 1

[Maximum number: 3]

0.200 mol sulfur dioxide, 0.300 mol oxygen and 0.500 mol sulfur trioxide were mixed in a 1.00dm31.00 \mathrm{dm}^{3} flask at 1000 K .

Predict the direction of the reaction showing your working.

Extent of Chemical Change Summary

Retrieve the route: define dynamic equilibrium, write K, interpret its magnitude, predict Le Châtelier shifts, compare Q with K, solve a RICE table, and connect K with ΔG.

Check closed-system and equal-rate language, exponents and direction, whether a change affects K, current versus equilibrium concentrations, stoichiometric x changes, and kelvin/unit consistency in ΔG calculations.