In the next step, the negatively charged intermediate undergoes an elimination reaction. This step leads to the loss of the bromine atom and the formation of a double bond between the carbon atoms.
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2-[1-(4-CHLOROPHENYL)ETHYLIDENE]MALONONITRILE
D-menthyl isobutyrate
Benzonitrile, 4-(ethenyloxy)-
4-(3',5'-dimethoxyphenyl)-1-(1-tetrahydrofuranyl)imidazole
bis(μ-carbonyl)(μ-o-xylylene)bis[(η-cyclopentadienyl)cobalt]
(2-methyl-5-methoxyl-1H-indol-3-yl)(phenyl)methanone
methylmalononitrile anion
4,4'-dichlorodiphenylmethyl (phenylsulfonyl)methyl sulfoxide
seleno-(o-methoxyphenyl) p-tolueneselenosulfonate
2-Propenoic acid, 3-phenyl-3-(phenylthio)-, methyl ester, (E)-
2-(2-(1,3-diphenyl-1H-pyrazol-5-yl)propan-2-yl)-N-methylaniline
3
(S)-1-tert-butyl 5-ethyl 2-(diphenylmethylene-amino)-4-methylenepentanedioate
ethyl 2-(benzoyloxymethyl)acrylate
