Audited 31 Jul 2026·Last updated 28 Oct 2026·3 citations·Tier 3·0 uses

Reaction Quotient Calculator

Compute the reaction quotient Q for aA + bB ⇌ cC + dD from the activities and coefficients of four species, ready to compare with K for that reaction.

Reaction Quotient Calculator

Reaction quotient
0.1667
The products' activities raised to their coefficients divided by the reactants' — a dimensionless number to compare with K for the same equation.
Model scope
Four-species dimensionless-activity expression supplied by the user; it does not balance a reaction, convert concentration/pressure to activity, include omitted species, or compare Q with an equilibrium constant.

Background.

A reacting mixture carries a record of where it stands relative to equilibrium at every moment, and the reaction quotient reads it. Take each product's activity — its effective concentration or pressure expressed as a pure number — raise it to the power of its coefficient in the balanced equation, multiply the results together, and divide by the same product for the reactants. For aA + bB ⇌ cC + dD, that gives Q = (a_C)^c (a_D)^d / ((a_A)^a (a_B)^b).

Q has exactly the form of the equilibrium constant K. The difference is that K uses the activities a system settles at, while Q uses whatever is present now, so comparing the two tells you which way the reaction will move. If Q is smaller than K there are too few products for equilibrium and the reaction runs forward; if Q is larger it runs in reverse; if they are equal, nothing changes on balance. Thermodynamics says the same thing through ΔG = ΔG° + RT ln Q, which is negative, meaning the forward reaction is spontaneous, precisely when Q is less than K.

Activities are where most errors creep in. For a gas behaving ideally, activity is partial pressure divided by the standard pressure of 1 bar; for a dilute solute it is concentration divided by 1 mol/L; pure solids and liquids, such as a precipitate or the water in a dilute aqueous solution, have an activity of 1. In concentrated solutions or at high pressure, real activities drift away from those approximations, and the values you enter are used as given.

All four slots are always in the expression. For a reaction with fewer species, set the unused activity to 1 — any power of 1 is 1, so it drops out. Balancing the equation and comparing Q with K remain your steps.

What is reaction quotient calculator?

The reaction quotient Q is a dimensionless number built from the activities of the species in a reaction at a particular moment: the product of the products' activities, each raised to its stoichiometric coefficient, divided by the corresponding product for the reactants. It is defined for any composition, not just equilibrium. When the mixture reaches equilibrium, Q becomes equal to the equilibrium constant K for the same written equation and temperature.

How to use this calculator.

  1. Write the balanced equation and assign the two reactants to A and B and the two products to C and D, in the direction you want Q for.
  2. Convert each amount to an activity: partial pressure in bar for an ideal gas, molar concentration in mol/L for a dilute solute, and 1 for a pure solid, pure liquid or solvent.
  3. Enter each species' coefficient from the balanced equation. Fractions such as 0.5 are accepted, and each coefficient can be at most 100.
  4. If the reaction has only three species, or two, enter an activity of 1 for each empty slot; its coefficient then makes no difference.
  5. Compare the resulting Q with the K for the same written equation at the same temperature: smaller means the reaction proceeds forward, larger means it proceeds in reverse.

The formula.

Q = a_C^c a_D^d / (a_A^a a_B^b)

Q = (a_C)^c (a_D)^d / ((a_A)^a (a_B)^b). Each activity is raised to its stoichiometric coefficient, so a species with coefficient 2 counts squared and one with coefficient 3 counts cubed; that is why a high-coefficient species usually dominates how Q responds to a change in conditions. Products sit in the numerator and reactants in the denominator, so adding product raises Q and adding reactant lowers it. Because activities are ratios to a standard state, Q has no units. Writing the equation differently changes Q in a predictable way: reversing it gives 1/Q, and multiplying every coefficient by two squares it. K transforms identically, which is why Q must always be compared with a K tabulated for the same written form. All activities and coefficients must be positive.

A worked example.

Example

Consider the water–gas shift reaction, CO + H₂O ⇌ CO₂ + H₂, in a gas mixture with partial pressures of 0.8 bar CO, 0.6 bar H₂O, 0.2 bar CO₂ and 0.4 bar H₂. Treating the gases as ideal, those pressures in bar are the activities, and every coefficient is 1. The products give 0.2 × 0.4 = 0.08 and the reactants 0.8 × 0.6 = 0.48, so Q = 0.08 ÷ 0.48 = 0.1667, exactly one sixth. If K at the reactor temperature is larger than 0.1667, the mixture still has room to make more CO₂ and H₂. Two contrasts show how Q behaves. Raising the hydrogen to 1.2 bar triples the numerator and gives Q = 0.5. Writing the equation with every coefficient doubled squares Q to 0.027778 — but the matching K is squared too, so the forward-or-reverse verdict is unchanged.

activity A0.8
activity B0.6
activity C0.2
activity D0.4
coefficient D1
coefficient C1
coefficient B1
coefficient A1

Frequently asked questions.

What is the difference between Q and K?
They are built from the same expression, but K uses the activities at equilibrium, at a given temperature, while Q uses the activities at any moment you choose. K is a fixed property of the reaction at that temperature; Q changes as the reaction proceeds and becomes equal to K once equilibrium is reached.
How do I convert concentrations or pressures to activities?
For ideal gases, divide the partial pressure by the standard pressure of 1 bar, so 0.8 bar becomes 0.8. For dilute solutes, divide the concentration by 1 mol/L. At high concentrations or pressures, activity coefficients or fugacities are needed for accuracy, and this page does not estimate them.
My reaction has only three species. How do I enter it?
Use the four slots for the species you have and give the spare slot an activity of 1. Since 1 raised to any power is 1, it neither multiplies nor divides the result. The same trick handles pure solids and liquids, whose activity is 1 by convention.
Why are pure solids and liquids left out of Q?
Their activity is 1 because their effective concentration does not change as the reaction proceeds — a lump of solid carbonate is just as pure whether there is a gram or a kilogram of it. Including them as 1 or leaving them out gives the same Q.
Does the way I write the balanced equation matter?
Yes. Reversing the equation turns Q into 1/Q, and multiplying every coefficient by a factor raises Q to that power. The direction it predicts does not change as long as K is written for exactly the same equation, so take your K value from a source that uses the same form.
Can a stoichiometric coefficient be a fraction?
Yes. Equations are sometimes written per mole of one product, as in H₂ + ½O₂ ⇌ H₂O, giving oxygen a coefficient of 0.5. Any positive coefficient up to 100 is accepted. Remember that K must then be the value for the fractional form, which is the square root of the K for the whole-number version.

How this page was produced

Published by
Quanta Calculator
Primary sources
3 cited below
Method
Q = a_C^c a_D^d / (a_A^a a_B^b)
Published
Last verified

Built with AI assistance and verified by automated tests against the cited sources — every worked example on this page is computed by the same code that runs the calculator. How we build and check calculators.

In this category

Embed

Quanta Pro

Paid features are coming later.

  • All 1560 calculators remain free
  • No billing is enabled
Coming soon