Linked from

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

• 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.

• PentadecaneCompared with: Unlike pentadecane, an alkene has a carbon–carbon multiple bond and fewer hydrogens.

• UndecaneCompared with: Unlike undecane, an alkene has a carbon–carbon multiple bond and fewer hydrogens.

• 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.

• Sorbic acidRelated: Sorbic acid contains two carbon–carbon double bonds in its carbon chain.

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

• E1cB elimination reactionBroader topic: The intermediate collapses as the double bond forms and the leaving group departs.

• Ei mechanismRelated: Ei commonly forms an alkene by removing neighboring substituents.

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

• Open-chain compoundBroader topic: Open-chain alkenes are reactive feedstocks for making polymers and chemicals.

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

• Vinyl alcoholRelated: Vinyl alcohol contains a carbon–carbon double bond, a defining feature of its enol structure.