The extent to which cations and anions in ionic liquids (ILs) and ionic liquid solutions are dissociated is of both fundamental scientific interest and practical importance because ion dissociation has been shown to impact viscosity, density, surface tension, volatility, solubility, chemical reactivity, and many other important chemical and physical properties. When mixed with solvents, ionic liquids provide the unique opportunity to investigate ion dissociation from infinite dilution in the solvent to a completely solvent-free state, even at ambient conditions. The most common way to estimate ion dissociation in ILs and IL solutions is by comparing the molar conductivity determined from ionic conductivity measurements such as electrochemical impedance spectroscopy (EIS) (which measure the movement of only the charged, i.e., dissociated, ions) with the molar conductivity calculated from ion diffusivities measured by pulse field gradient nuclear magnetic resonance spectroscopy (PFG-NMR, which gives movement of all of the ions). Because the NMR measurements are time-consuming, the number of ILs and IL solutions investigated by this method is relatively limited. We have shown that use of the Stokes-Einstein equation with estimates of the effective ion Stokes radii allows ion dissociation to be calculated from easily measured density, viscosity, and ionic conductivity data (ρ, η, λ), which is readily available in the literature for a much larger number of pure ILs and IL solutions. Therefore, in this review, we present values of ion dissociation for ILs and IL solutions (aqueous and nonaqueous) determined by both the traditional molar conductivity/PFG-NMR method and the ρ, η, λ method. We explore the effect of cation and anion alkyl chain length, structure, and interaction motifs of the cation and anion, temperature, and the strength of the solvent in IL solutions.