A mathematical model of multivinyl monomer free radical photopolymerizations that takes into account chain length dependent termination (CLDT) and gel formation (an infinite network) was utilized to obtain a more accurate picture of network formation and multivinyl monomer photopolymerization kinetics. The model predicts an increased probability that a radical chain is attached to the gel with increasing chain length and double bond conversion. Accounting for CLDT delays radical incorporation into the gel and induces gel formation at earlier double bond conversions. Increasing the initiation rate also delays gel formation. When the model is expanded to account for the probability that a highly mobile sol radical reacts to become a nearly immobile gel radical, the importance of CLDT prior to reaction diffusion-controlled termination is increased. This result is attributed to bimolecular termination occurring between a short (< 10-mer) sol radical and a long gel radical (short-long radical termination). The transition from a CLDT important regime to reaction diffusion-controlled termination is characterized by a transition from primarily short-long to primarily long-long (gel-gel) radical termination.