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Reaction spontaneity calculator

A reaction with ΔH of −100 kJ/mol and ΔS of −50 J/(mol·K) at 298.15 K has ΔG of −85.0925 kJ/mol, so it is spontaneous. Type the values straight from your table; the entropy is scaled from joules to kilojoules for you. Free in your browser.

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If you enter
Enthalpy
-100
Entropy
-50
Creativity
298.15
You get
Delta g
-85.0925
Delta G
-85.0925
Gibbs energy
-85.0925
Delta h
-100

Whether a chemical change can proceed spontaneously under constant temperature and pressure is decided by the sign of the Gibbs free energy change. Given the enthalpy change ΔH, the entropy change ΔS, and the absolute temperature T in kelvin, this capability evaluates ΔG = ΔH − T·ΔS with a deterministic pure-arithmetic path and returns both the numeric free energy and a clear classification: spontaneous when ΔG is negative, non-spontaneous when positive, and equilibrium when zero. Textbook tables often pair kilojoule enthalpies with joule entropies; by default the engine scales entropy by one thousandth so T·ΔS matches the enthalpy energy unit, while an explicit entropy unit of kJ or same leaves ΔS unchanged. Negative temperatures fail with invalid input instead of inventing physics.

The sign that decides spontaneity

At constant temperature and pressure, whether a reaction can proceed by itself is decided by the sign of the Gibbs energy change, ΔG = ΔH − T·ΔS. You bring the enthalpy change, the entropy change and the absolute temperature in kelvin; the calculator returns ΔG and a plain label. Below zero the forward reaction is spontaneous, above zero the reverse is favoured as written, and at exactly zero the system sits at equilibrium for that temperature. Nothing is looked up in tables, so the answer depends only on the numbers you enter.

Joules, kilojoules and the most common slip

Most textbooks list ΔH in kilojoules per mole but ΔS in joules per mole-kelvin. Multiplying the two without converting gives a ΔG that is wrong by a long way. That is why the entropy is divided by 1000 by default. With ΔH of −100 kJ/mol, ΔS of −50 J/(mol·K) and 298.15 K, the T·ΔS term is −14.9075 kJ/mol and ΔG is −85.0925 kJ/mol. If your entropy is already in kilojoules, pick the same-unit option. A negative temperature is refused, and a missing value is named so you can fix the blank cell.

Reading the response: ΔG, T·ΔS, and classification

Validation messages that mention negative temperature or missing enthalpy, entropy, or temperature name the field so you can fix a blank cell without reading a stack trace. Keep one energy convention for the whole request: mixing unscaled joule entropies with kilojoule enthalpies without the default J unit would yield a wrong free energy.

Homework and exam verification

Students enter ΔH, ΔS, and T, compare the returned ΔG and spontaneity label with hand work, and get a clear error when temperature is negative or a field is missing.

What happens if temperature is negative?

Absolute temperature on the kelvin scale must be non-negative for this calculator.

Is the reaction spontaneity calculator free?

The browser tool runs free on your device.

Do I need to convert entropy from joules to kilojoules first?

No. By default the entropy is read as joules per mole-kelvin and divided by 1000, so it matches an enthalpy in kilojoules. If your ΔS is already in kilojoules, choose the same-unit option and it is used as it is.

What does a negative ΔG tell me?

It means the reaction runs forward on its own at that temperature and pressure. A positive ΔG means the reverse direction is favoured, and a ΔG of exactly zero means the system is at equilibrium.

Does the calculator look up enthalpy or entropy tables?

No. You supply the three numbers, ΔH, ΔS and the temperature in kelvin, from your textbook or data sheet. The calculator does the arithmetic and the classification, nothing more.

Everything on this page is available programmatically. This section is for teams who want to wire it into their own systems; everyone else can just use the tool above.

POSThttps://api.kit.forhosting.com/chem/gibbs-spontaneity

Prefer to automate it? One authenticated POST creates the task; the result comes back by webhook or a signed link. The same capability also runs here on the web, by email and from Telegram — and soon from our app too.

curl -X POST https://api.kit.forhosting.com/chem/gibbs-spontaneity \
  -H "Authorization: Bearer $KIT_KEY" \
  -H "Content-Type: application/json" \
  -d '{"enthalpy":-100,"entropy":-50,"temperature":298.15}'
{
  "enthalpy": -100,
  "entropy": -50,
  "temperature": 298.15
}
{
  "task_id": "tsk_a1b2c3d4e5f6a1b2c3d4e5f6",
  "type": "chem.gibbs_spontaneity",
  "status": "queued",
  "_links": {
    "result": "/tasks/tsk_…/result"
  }
}

The API is asynchronous: the call returns a task_id immediately and the result arrives by webhook. Polling is capped at 1 req/s per task.

Per request$0.002

Published price — no tokens, no invented credits. A failed task is never charged.

HTTPCodeMeaning
401unauthorizedMissing or invalid API key.
402insufficient_balanceYour balance doesn't cover the task price.
404unknown_typeThat task type doesn't exist.
429rate_limitedToo many requests. Use the webhook instead of polling.

How Gibbs free energy decides reaction spontaneity

At constant temperature and pressure, the change in Gibbs free energy is the thermodynamic criterion for spontaneity of a process as written. Collect a reaction enthalpy ΔH and a reaction entropy ΔS in consistent bookkeeping, choose the absolute temperature T in kelvin, and evaluate ΔG equals ΔH minus T times ΔS. When ΔG is less than zero the forward process is thermodynamically spontaneous under those conditions; when ΔG is greater than zero the reverse direction is favored as written; when ΔG is exactly zero the system sits at equilibrium for that temperature. The engine does not look up formation tables: you supply the three numbers (or their aliases enthalpy, entropy, temperature and the common delta_h, delta_s, T forms). Optional energy_unit is a display label only, defaulting to kJ/mol for ΔH and ΔG. Optional entropy_unit defaults to J so that tabulated J per mole kelvin entropies are scaled by one thousandth before multiplication by T, matching kilojoule enthalpies used in most classroom problems; set entropy_unit to kJ or same when your ΔS is already in the same energy unit as ΔH. Negative temperature is rejected with invalid_input because absolute temperature cannot be negative on the kelvin scale for this calculator. Identical inputs always produce identical JSON because the path is pure arithmetic with no network call, no model, no random seed, and no wall clock.

Reading the response: ΔG, T·ΔS, and classification

On success the response includes delta_g, the alias delta_G, and gibbs_energy—all equal to the computed free energy—plus enthalpy and delta_h echoes of the input ΔH after stable rounding. delta_s_input preserves the raw entropy you sent; delta_s, delta_S, and entropy report the value after optional joule-to-kilojoule scaling; temperature and T echo kelvin; t_delta_s is the T times scaled ΔS product subtracted from enthalpy. energy_unit and entropy_unit document the labels used, and entropy_scale is one for same-unit entropy or zero point zero zero one when joule scaling applied. classification is spontaneous, non_spontaneous, or equilibrium; spontaneous is a boolean true only for the first case so UI badges need no extra sign logic. formula restates ΔG = ΔH − T·ΔS, and method is always gibbs_free_energy so downstream code can branch without sniffing shapes. Use delta_g alone when a spreadsheet or gradebook needs a single number; use t_delta_s when a lab report must show how the entropy term competes with enthalpy at high temperature.

API usage, pricing, classroom labs, and practical limits

Call the free in-browser reaction spontaneity calculator for homework checks, lecture demos, and quick lab prep without installing a thermochemistry package. The capability never converts Celsius to kelvin for you—add two hundred seventy-three point fifteen yourself—and never invents missing thermochemical table values. Send a JSON body with required numbers enthalpy, entropy, and temperature; aliases delta_h, dH, H, delta_s, dS, S, T, temp, kelvin, and temp_K are accepted when documented by the SDK. Use the prepaid API when a tutoring platform, process-safety worksheet, materials screening helper, or curriculum generator needs a stable contract under KIT balance at $0.002 per successful item; validation failures never consume balance after the engine rejects the request. Pair this endpoint with enthalpy-of-reaction or entropy-of-reaction helpers when you first build ΔH and ΔS from formation or standard molar data, then feed those aggregates here with a process temperature. Authors shipping SDKs can map classification and spontaneous into badges, and expose delta_g with energy_unit as the primary numeric column students compare to hand work.

Teaching apps and auto-graded drills

Curriculum tools generate Gibbs-energy exercises with structured JSON for flashcards, rubrics, and step sheets without embedding a full thermochemical database.

Lab notebooks and process calculators

Scripts convert supplied ΔH and ΔS tables into free energies and spontaneity flags for safety sheets, energy balances, and teaching demos via a stable prepaid endpoint.

How do I calculate Gibbs free energy and reaction spontaneity?

Send JSON with enthalpy (ΔH), entropy (ΔS), and temperature in kelvin. The response includes delta_g equal to ΔH minus T·ΔS and classification spontaneous, non_spontaneous, or equilibrium.

Why is entropy scaled by 1/1000 by default?

Default entropy_unit is J so textbook ΔS values in J/(mol·K) match ΔH in kJ/mol. Set entropy_unit to kJ or same when ΔS is already in the same energy unit as ΔH.

Does a negative ΔG mean the reaction is spontaneous?

Yes as written under constant T and P: classification is spontaneous when delta_g is negative, non_spontaneous when positive, and equilibrium when zero. Reverse the process and the sign flips.

Read the full KIT documentation →