Wats E1CB?
c6h5-ch2-chF-CH3 ON DOING E1CB WILL FORM SAYTZEFF ALKENE OR HOFFMAN
-
UP 0 DOWN 0 0 14
14 Answers
Dr.House
·2009-02-19 08:22:00
in e1cb first electrophile goes then nucleophile goes.
. A strong base abstracts the α proton generating a carbanion. The electron pair then expels the leaving group and the double bond is formed.
sry edited..........
Dr.House
·2009-02-19 08:29:19
u mean saytzeff alkene is the answer? (then i got to think a bit){hehehe}
°ღ•๓ÑÏ…Î
·2009-02-19 11:09:27
it will form hoffman whenevr we hav F we get hoffman product in e1cb
Debotosh..
·2009-08-20 10:33:15
definitely the hoffmann mechanism will predominate because of the presence of strong electron withdrawing group...fluorine !