Linked from

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

• Cis–trans isomerismRelated: A double bond can prevent rotation and support cis–trans arrangements.

• Geometric isomerismRelated: The double bond’s restricted rotation commonly produces geometric isomers.

• Cahn–Ingold–Prelog priority rulesRelated: Its restricted rotation can create geometric stereoisomers labeled with E/Z descriptors.

• EnolRelated: An enol combines an alkene-like bond with a hydroxyl substituent on one alkene carbon.

• CycloadditionRelated: Alkenes commonly supply a two-atom unit in cycloaddition reactions.

• EpoxideRelated: Alkenes are common starting materials for epoxide synthesis by epoxidation.

• E1 reactionRelated: Alkenes are the products formed when a base removes a beta proton from the E1 intermediate.

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

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

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