2.3.5 (HL)—Reaction quotient (Q)
- Syllabus
- First assessment 2025
- Objective
- 2.3.5
- Level
- HL
Q=product−over−reactantconcentrationexpressionusingcurrentconcentrations
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 Q example: for NX2(g)+3HX2(g)2NHX3(g), Q=[NHX3]2/([NX2][HX2]3). If every current concentration is 0.50moldm−3, Q=(0.50)2/[(0.50)(0.50)3]=4.0. At 475 K, K=0.59, so Q>K: the mixture contains too much product relative to equilibrium and the reverse direction is favoured until Q=K.
Representative question
0.200 mol sulfur dioxide, 0.300 mol oxygen and 0.500 mol sulfur trioxide were mixed in a 1.00dm3 flask at 1000 K .
Predict the direction of the reaction showing your working.
«reaction quotient /Q=»[SO2]2[O2][SO3]2/0.2002×0.3000.5002/20.8∨
reaction quotient/Q/20.8/answer < Kc /280 OR mixture needs more product for the number to equal Kc∨
reaction proceeds to the right/products
Marking guidance:
Do not award M3 without valid reasoning.
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.