The data on the cleavage of sigma-bonds by electroreduction, found in the l
iterature and obtained by the authors, are analyzed. A new EED mechanism is
proposed. It is shown, using reactions of reduction of various organic com
pounds (halogenorganic compounds, ethers, organic phosphates, nitroamines),
that this is a rather common reaction path. The EED processes are intermed
iate between processes EDE and ECE. If the reorganization of reacting speci
es in the first electron transfer is minimal, either E or ECE process is re
alized; with maximum reorganization, the EDE process; and at intermediate v
alues, the EED process.