Home Chemistry Organic Building Blocks Ketones Ethene-1,1-Diyldibenzene
Electrophilic Aromatic Substitution: The benzene rings in stilbene can undergo electrophilic aromatic substitution reactions. For example, you can nitrate or sulfonate the benzene rings using appropriate reagents.
Diels-Alder Reaction: Stilbene can participate in Diels-Alder reactions with suitable dienophiles, forming a six-membered ring with the elimination of the double bond.
Bromination or Halogenation: Stilbene can undergo halogenation reactions. For example, you can brominate stilbene in the presence of bromine to form dibromostilbene.
Hydrogenation: The carbon-carbon double bond in stilbene can be hydrogenated to form a completely saturated compound (1,2-diphenylethane) using hydrogen gas and a suitable catalyst, such as palladium or platinum.
Oxidation: Stilbene can be oxidized to produce various products. For example, you can use potassium permanganate to oxidize stilbene to form two molecules of benzaldehyde.
Isomerization: Under certain conditions, stilbene can undergo isomerization, converting from the E (trans) isomer to the Z (cis) isomer and vice versa.
Reduction: Stilbene can be reduced using reducing agents like sodium borohydride to produce 1,2-diphenylethylamine.
Wittig Reaction: Stilbene can be used as a substrate in a Wittig reaction to synthesize alkenes with a specific configuration.
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1-Chloro-4-(1-phenylvinyl)benzene
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1-Chloro-2-(1-phenylvinyl)benzene
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