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Integrated Rate Law Solver
The current ledger marks this instrument verified clean within the source-bound verification corpus.
Inspectable records
Ledger state
The current ledger marks this instrument verified clean within the source-bound verification corpus.
- Area
- Chemistry & Materials
- Tranche
- tranche-6
- Evidence ID
- t6-119
- Ledger rows
- 1
No ledger note is attached.
Review findings
The three displayed integrated rate laws are standard and mathematically correct under their assumptions. Verdict is NEEDS_REVIEW because the specification does not define inverse-solving formulas, admissible domains, exact unit handling, or deterministic plotting bounds, and it does not explicitly label the model as an irreversible constant-condition single-reactant approximation.
Formula and scope findings
- The listed integrated laws are correct for irreversible, single-reactant reactions with constant volume and constant temperature, but the solver must explicitly provide the inverse forms for the claimed 'solve for any one' capability: zero-order t=([A]0-[A])/k, first-order [A]=[A]0 exp(-kt) and t=ln([A]0/[A])/k, and second-order t=(1/[A]-1/[A]0)/k.
- The specification does not state the required physical-domain constraints: [A]0>0, [A]>=0, t>=0, and k>0 for a consuming reaction. Zero-order calculations become physically invalid when t>[A]0/k; first- and second-order target concentrations must satisfy 0<[A]<=[A]0.
- The phrase 'solve for any one' is ambiguous because the declared inputs include order, k, [A]0, and t but do not identify whether [A], k, [A]0, or t may be the missing variable, nor how the solver represents a target concentration.
- The plotting output is underspecified: no time range, sampling resolution, or handling of the physically invalid negative-concentration portion of a zero-order curve is defined.
Unit assumptions
- Concentration [A] and [A]0 use the same concentration unit, such as mol/L (M).
- Time t and the rate constant k must use compatible units.
- For zero order, k has concentration/time units, such as M/s.
- For first order, k has inverse-time units, such as s^-1 or min^-1.
- For second order, k has concentration^-1 time^-1 units, such as M^-1 min^-1.
- The formulas assume an irreversible reaction involving one tracked reactant concentration, constant volume, constant temperature, and a constant rate constant.
Boundary hardening
BREAK_CLAIMED · SELF_FLAGGED
The zero-concentration second-order request causes division by zero and must not produce an ordinary numeric time. Negative-k handling is also underspecified: literal arithmetic gives growth, while the conventional rate-constant interpretation should reject the input.
Errata and corrections
No applied erratum is attached to this unique-name record.
Inspectable example
4 review vectors are recorded. One source-bound sample is shown below.
{
"inputs": {
"order": 0,
"k": 0.0025,
"k_units": "M/s",
"A0": 0.1,
"A0_units": "M",
"t": 20,
"t_units": "s",
"solve_for": "A"
},
"expected_outputs": {
"A": 0.05,
"A_units": "M",
"sampled_points": [
{
"t": 0,
"A": 0.1
},
{
"t": 20,
"A": 0.05
},
{
"t": 40,
"A": 0
}
],
"curve_features": {
"slope": "-0.0025 M/s",
"zero_concentration_time": 40,
"zero_concentration_time_units": "s",
"valid_nonnegative_domain": "0 <= t <= 40 s"
}
},
"working": "Zero-order law: A=A0-kt. At t=20 s, kt=(0.0025 M/s)(20 s)=0.0500 M. Therefore A=0.100 M-0.0500 M=0.0500 M. Boundary check: at t=A0/k=(0.100 M)/(0.0025 M/s)=40.0 s, A=0; for t>40.0 s the algebraic result is negative and is not a physical concentration."
}Related workflows
No source-defined multi-instrument workflow membership is recorded.
Sources and evidence
These pointers bind the page to evidence. They do not grant authority or collapse verification into deployment.
VERIFIED_LEDGER.json · VERIFIED_CLEANevidence-tranche6/tranche6-results.jsonBOUNDARY_HAZARD_CATALOG.json