The translational diffusion constants, D, for solutes with polymethylene chains are compared with the predictions of a hydrodynamic bead model based on Kirkwood-Riseman theory. The solute-solvent combinations include (a) n-alkanes in n-alkanes; (b) n-alkanes in benzene, toluene, tetralin, decalin, and CCl4; (c) 1-alkenes in n-alkanes; (d) 1-phenylalkanes in n-alkanes; and (e) 1-phenylalkanes in isocetane (2,2,4,4,6,8,8-heptamethylnonane), pristane (2,6,10,14-tetramethylpentadecane), and squalane (2,6,10,15,19,23-hexamethyltetracosane). The bead model gives good overall agreement with an average difference of less than 3% between 207 experimental and calculated diffusion constants that include published data as well as new D values determined for 1-alkenes and 1-phenylalkanes using capillary flow techniques. The calculated values are obtained using chain element (bead) radii that decrease as the solvent viscosity increases. The bead model's results are comparable to those obtained using cylinder and lollipop diffusion for many of the same solute-solvent systems; the three models are compared and discussed. The results for the 1-alkenes and n-alkanes in the n-alkanes are the first from a Kirkwood-Riseman analysis in a homologous series of solvents.