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An isocyanate bears an $\mathrm{R}-\mathrm{N}=\mathrm{C}=\mathrm{O}$ group. A molecule bearing two such groups can react with a diol to form polyurethane connections.

A polyurethane contains repeated connections of the form $-\mathrm{O}-\mathrm{C}(=\mathrm{O})-\mathrm{NH}-$. Suitable hydroxy groups and isocyanate groups can produce those connections by polyaddition; exactly two suitable groups per feed molecule give the bifunctional linear model only when competing reactions and ring closure are excluded.

An experimental comparison joined a two-ended diol chain, HOPCLOH, with a bifunctional isocyanate, at reported isocyanate-to-diol ratio $1.14:1$. The researchers used oven-dried $25\mathrm{mL}$ round-bottom flasks and an IKA RET magnetic hotplate with a metal carrier. They varied solvent, concentration, reaction temperature ($50$ or $61{}^{\circ }\mathrm{C}$), and duration ($1$ or $8\mathrm{h}$).^[ref]

A Bruker $500\mathrm{MHz}$ NMR spectroscopy instrument measured residual hydroxy group-adjacent signal relative to an ester signal. Independently, size-exclusion chromatography used ResiPore columns at $70{}^{\circ }\mathrm{C}$, a refractive-index detector, and polystyrene calibration. Figure 8 reports sharply increasing apparent number-average molar mass beyond the reported conversion $0.95$. A deliberately water-exposed isocyanate comparison reproduced a $1625\mathrm{c}{\mathrm{m}}^{-1}$ infrared spectroscopy band assigned to urea-containing products. The authors warn that tiny residual NMR spectroscopy signals reduce integration precision.^[ref]

The inference is increasing chain size alongside depletion of reactive groups, consistent with step-growth polymerization. It is not an exact measurement of $X_n$ in the toy model. The feed contains already extended diol chains: counting their constituent repeat units differs from counting each feed molecule as one unit. Their varying molar masses, calibration against a different polymer, residual starting material, and competing chemical reactions further obstruct a direct conversion-to-$X_n$ substitution. Report which functional groups the conversion readout measures before comparing it with stoichiometric imbalance in step growth.

Useful proposed controls, distinct from the reported water comparison, are pre-reaction spectra and matched mixtures omitting each joining partner in turn. Keep solvent, heating, and signal normalization matched. Disappearance of an isocyanate signal in the omitted-diol control would reveal competing consumption rather than establish chain joining. Agreement between residual-group and independently calibrated chain-size readouts is stronger evidence than calculating both quantities from the same Carothers equation.

In step-growth polymerization, suitable reactive groups on molecules of different chain lengths can join. The linear count and its assumptions are given in polymerization.

A one-unit monomer, a two-unit chain, and a twenty-unit chain can all be joining partners if their functional groups are compatible and accessible. Schematically, $P_j+P_k⟶P_{j+k}$: the subscripts count monomeric units, and end-group chemistry is suppressed. In chain-growth propagation, by contrast, $P_j^{\ast }+M⟶P_{j+1}^{\ast }$ requires a free monomer and a polymerization-active site. An arbitrary pair of existing chains is not a propagation pair in that mechanism. The practical consequence of step-growth polymerization is that most monomers can have joined something while the average chain is still short.

Whether a joining step releases a small molecule is a separate question. Polycondensation releases small products during the joining chemistry, as in the Nylon 6,10 demonstration in polymerization. Polyaddition joins suitable chains without that elimination: reacting a diol with a molecule bearing two isocyanate groups can build a polyurethane. Thus step-growth polymerization and polycondensation are not synonyms.^[ref]