| 摘 要： | Relative reactivities of polyhalofluoroalkanes toward bromophilic or chlorophilic attacks have been evaluated for the first time by comparing the rates of halophilic attacks by a carbanion derived from the addition of a nucleophile to an olefin with the rate of β-elimination of the same carbanion intermediate. Relative reactivity orders of some polybromofluoroalkanes and polychlorofluoroalkanes are CF_2Br_2>CF_3CFBr_2 ～ CF_2BrCF_2Br>CF_3CBr_3, and CCl_4 > CF_3CCl_3 > CF_2ClCCl_3 > CFCl_3 > CFCl_2CFCl2 ～ CF_2ClCFCl_2. Early transition states for halophilic attacks are speculated.
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