The present study investigates the standard model of [1,2]-fluorine migration and that triggered by the rearrangement of cyclopropyl-substituted fluoroepoxides. The [1,2]-fluorine migration reaction proceeds via a synchronous concerted, tight-ion-pair mechanism. When coupled with other reaction coordinates, the whole reaction follows an asynchronous mechanism, while the [1,2]-fluorince migration unit still retains its tight-ion-pair feature and the reaction coordinates of two C-F distances vary synchronously. A general reaction program for α-electron-deficiency-induced [1,2]-fluorine migration is proposed through an analysis of the intermediates generated from nucleophilic addition. The reaction mechanisms associated with α-electron deficiency and the rearrangement are scrutinized using computational chemistry. Two additional reaction programs for [1,2]-fluorine migration are identified. The Gibbs free energy change of [1,2]-fluorine migration exhibits a linear dependence on the value of the Fukui function of the substrate, which could lead to the production of the desired α-monofluoroketone and enhance the utilization of fluorine atoms.