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The 66 pages that link to Alkene, each with the reason it gives.

• Electrophilic additionNarrower topic: Its electron-rich pi bond is the usual site of electrophilic attack.

• EthyleneNarrower topic: Ethylene is the simplest member of this family of compounds.

• IsopreneNarrower topic: Isoprene is an alkene with two conjugated double bonds.

• E–Z notationNarrower topic: E–Z notation applies to the geometry around an alkene double bond.

• PropyleneNarrower topic: Propylene belongs to this family because it contains one carbon–carbon double bond.

• EtheneNarrower topic: Ethene is the simplest member of this hydrocarbon family.

• HydroformylationNarrower topic: Alkenes supply the carbon skeleton that hydroformylation extends.

• Addition polymerizationNarrower topic: Many addition-polymerization monomers are alkenes whose double bonds open during chain growth.

• Hydration reactionNarrower topic: Alkenes are common substrates for hydration across a carbon–carbon double bond.

• Markovnikov's ruleNarrower topic: Unsymmetrical alkenes provide the two nonequivalent positions whose reaction orientation the rule predicts.

• OzonolysisNarrower topic: Alkenes are the characteristic substrates whose double bonds ozonolysis cleaves.

• AcrylonitrileNarrower topic: Acrylonitrile’s alkene bond is the site of addition polymerization.

• Cationic polymerizationNarrower topic: Electron-rich alkenes are common monomers because a cation can add across their double bond.

• Hofmann eliminationNarrower topic: It is the carbon framework product formed by the elimination.

• sp² hybridizationNarrower topic: The carbon atoms at an alkene double bond are commonly sp²-hybridized.

• BrominationNarrower topic: The electron-rich double bond makes alkenes common substrates for bromine addition.

• Wittig reactionNarrower topic: This is the product class formed by the reaction.

• Acrylic acidNarrower topic: Acrylic acid’s alkene enables addition reactions and chain-growth polymerization.

• CyclohexeneNarrower topic: Cyclohexene is a cyclic member of this broader class.

• Fumaric acidNarrower topic: Fumaric acid’s double bond permits geometric isomerism and addition reactions.

• Addition reactionNarrower topic: Alkenes are the standard substrates for additions across a carbon–carbon π bond.

• Methyl methacrylateNarrower topic: The monomer's alkene bond is the site of chain-growth polymerization.

• Wacker processNarrower topic: Ethylene belongs to this family of substrates for palladium-catalyzed oxidation.

• CyclopentadieneNarrower topic: Cyclopentadiene contains two alkene units joined in a conjugated ring.

• Cinnamic acidNarrower topic: Cinnamic acid’s chain contains a double bond that permits E and Z forms.

• IsobutyleneNarrower topic: Isobutylene is a simple, branched member of this hydrocarbon family.

• Methacrylic acidNarrower topic: Methacrylic acid's alkene is the reactive site used in addition polymerization.

• Yves ChauvinNarrower topic: Alkenes are the substrates whose double-bond partners metathesis rearranges.

• Allyl alcoholNarrower topic: Allyl alcohol’s alkene group undergoes addition and polymer-forming reactions.

• CyclopropeneNarrower topic: Cyclopropene is the smallest cyclic member of this broad family.

• PropadieneNarrower topic: Propadiene contains two alkene-like carbon–carbon double bonds, though its consecutive bonds define a distinct structure.

• 1,1-DichloroethyleneNarrower topic: The compound’s reactive carbon–carbon double bond makes it an alkene.

• Free-radical additionNarrower topic: Its double bond is a common target for radical addition.

• Sulfur dichlorideNarrower topic: Sulfur dichloride adds to alkene double bonds, enabling sulfur-containing products.