Transition-state spectra are mapped out using generalized adiabatic electron-transfer theory. This simple model depicts diverse chemical properties, from aromaticity, through bound reactions such as isomerizations and atom-transfer processes with classic transition states, to processes often described as being "non-adiabatic", to those in the "inverted" region that become slower as they are made more exothermic. Predictably, the Born-Oppenheimer approximation is found inadequate for modelling transition-state spectra in the weak-coupling limit. In this limit, the adiabatic Born-Huang approximation is found to perform much better than non-adiabatic surfacehopping approaches. Transition-state spectroscopy is shown to involve significant quantum entanglement between electronic and nuclear motion. Highlights-transition-state spectra are calculated over a wide parameter region-spectral and temporal responses may be simple or quite complex-surface hopping methods fail to describe spectra usually classified as "non-adiabatic"-transition-state spectroscopy embodies quantum entanglement