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The 26 pages that link to Electrophilic addition, each with the reason it gives.

• AlkeneRelated: This common alkene reaction breaks the pi bond and forms two new sigma bonds.

• Pi bondRelated: The exposed electron density of a pi bond makes it a target for electrophiles.

• HydrocarbonRelated: Alkenes and alkynes react at their multiple bonds by addition.

• EthyleneRelated: Ethylene’s electron-rich double bond readily undergoes this reaction pattern.

• RegioselectivityRelated: Its competing orientations on an unsymmetrical alkene reveal regioselectivity.

• PropyleneRelated: The electron-rich double bond in propylene commonly reacts by addition.

• EtheneRelated: Many reagents add across ethene's carbon–carbon double bond by this mechanism.

• BrominationRelated: Bromine adds across alkene double bonds through an electrophilic pathway.

• CyclohexeneRelated: The double bond of cyclohexene undergoes additions such as halogenation and hydration.

• Double bondRelated: Many alkene reactions consume the pi component while forming two new single bonds.

• Aliphatic compoundRelated: Aliphatic alkenes and alkynes commonly react by addition at their multiple bonds.

• AziridineRelated: Electrophilic activation of aziridine nitrogen can promote nucleophilic ring opening.