Photoredox-based　C-H　bond　functionalization　constitutes　one　of　the　most　powerful　and　atom-economical　approaches　to　organic　syntheses.　During　this　type　of　reaction,　single　electron　transfer　takes　place　between　the　photocatalyst　(PC)　and　redox-　active　substrates.　Electrosynthesis　also　involves　electron　transfer　between　substrates　and　electrodes.　In　this　paper,　we　focus　upon　electrochemical　cross-coupling　of　C(sp(2))-H　with　aryldiazonium　salts　and　have　developed　an　efficient　electrochemical　approach　to　the　Minisci-type　arylation　reaction.　The　constant　current　paired　electrosynthesis　proceeds　in　a　simple　undivided　cell　without　external　supporting　electrolyte,　features　a　wide　range　of　substrates　and　is　easy　to　scale-up.　These　results　demonstrate　that　photoredox-based　cross-coupling　of　C(sp(2))-H　with　aryldiazonium　salts　can　also　proceed　successfully　under　paired　electrolysis　conditions,　thereby　contributing　to　understanding　of　the　parallels　between　photosynthesis　and　electrosynthesis.