Build an equilibrium particle diagram with an honest scale
Construct monomer and dimer counts, conserve constituent units, and convert weighted symbols and stated volume into the equilibrium quotient.
Learning outcome: Connect particulate composition, molar inventory and concentration while distinguishing species count from conserved constituent units.
Starting recap
In 2A ⇌ B, one B symbol contains two A units but represents one species. A diagram needs an amount scale and volume before counts can become concentrations.
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Try
Four monomer symbols and four dimer symbols have eight species symbols. How many constituent units do they contain, and does a raw count ratio determine K?
Open the experimentPredict
Predict whether doubling every symbol while halving its molar weight changes the physical state. Predict what changes if volume triples but symbol weights and conserved inventory do not.
Experiment
Build a conserved 1 L equilibrium diagram, then preserve the counts while changing volume to 3 L and inspect Q. Repair the composition. Change to finer symbols in the original volume and construct the same physical state with different counts. Capture two equivalent representations and explain their legends.
Build a particle diagram and read its physical legend
Worked teaching model · synthetic values · Original schematic 2A ⇌ B model, with each B containing two A units, assigned dimensionless K = 2.5 at fixed temperature and ideal concentration activities relative to 1 mol/L. A symbol represents a stated macroscopic molar amount of that species, not one literal molecule. Panel area and symbol positions do not encode volume, speed or intermolecular distance. No stochastic few-particle trajectory, experimental image or rate is claimed.
Reset keeps your prediction, captures and practice history.
Construct species, then count their constituent units
Reaction 2A ⇌ B. A single circle labeled A is a monomer symbol; a bonded pair labeled B is one dimer species symbol containing two constituent units. Each species symbol represents 0.10 mol. Volume is 1 L; assigned K = 2.5.
Species symbols: 12 + 0 = 12. Constituent-unit symbols: 12 + 2 × 0 = 12. The constituent inventory matches. Two A joining into one B reduce species count by one without losing constituent units.
| Species | Symbols | mol per species symbol | Represented amount (mol) | Concentration (mol/L) |
|---|---|---|---|---|
| A | 12 | 0.1 | 1.200 | 1.2000 |
| B | 0 | 0.1 | 0.000 | 0.0000 |
Represented constituent inventory = 1.200 mol; target = 1.200 mol. Q = ([B]/c°)/([A]/c°)² = 0.0000 / 1.2000² = 0.00000, with c° = 1 mol/L.
This is not an accepted equilibrium representation for this batch. A conserved diagram can still be out of equilibrium. A matching quotient can still describe the wrong amount of material.
Representation scale, volume and microscopic limits
For counts NA and NB and symbol weight w mol, [A] = wNA/V and [B] = wNB/V. Therefore Q = (NB/NA²)(V c°/w), when NA is nonzero. The raw count ratio alone is not the concentration quotient. Doubling both symbol counts while halving w preserves amounts, concentrations and Q; doubling counts without changing w does not.
At 1 L and weight 0.10 mol, A = 4 and B = 4 matches K. At 3 L the same inventory instead matches at A = 6 and B = 3. The finer 0.05 mol symbols in 1 L represent the first equilibrium with A = 8 and B = 8. These are weighted macroscopic composition diagrams, not literal few-particle states with deterministic equilibrium. Locations are layout choices, not evidence of speeds, bonds forming over time or measured distances.
Check conserved constituent units and the volume-weighted quotient separately.
12 species symbols contain 12 constituent-unit symbols. Represented inventory 1.200 versus target 1.200 mol of units. Q = 0.00000.
Captures preserve recipes and replay their calculated results. They are synthetic model evidence, not physical measurements.
Understand
Apply
Public practice checks a specific claim. It does not establish independent mastery.
Explain the distinction among symbols, species, constituent units, moles and concentration. State why the panel area and a few drawn particles do not establish microscopic equilibrium or actual vessel dimensions.
Continue
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