Linked from

The 28 pages that link to Electrophile, each with the reason it gives.

• Nucleophilic substitutionRelated: The electrophilic atom attached to the leaving group is the site of attack.

• Electrophilic aromatic substitutionBroader topic: The electrophile accepts electron density from the aromatic ring in the bond-forming step.

• Lewis acidRelated: Electrophiles often behave as Lewis acids, though the terms emphasize different aspects of reactivity.

• Functional groupRelated: Electrophilic atoms are common reaction sites within polarized functional groups.

• NucleophileRelated: It accepts the pair that a nucleophile supplies.

• Nucleophilic additionNarrower topic: The polarized multiple bond contains the electron-poor site attacked in the addition.

• Electrophilic additionNarrower topic: It initiates addition by accepting electron density from the multiple bond.

• SN2 reactionRelated: The electrophilic carbon is the site attacked by the SN2 nucleophile.

• Lewis baseCompared with: Electrophiles play the accepting role opposite Lewis bases in bond-forming reactions.

• Friedel–Crafts reactionNarrower topic: The key reagent-derived species attacks the aromatic ring in each Friedel–Crafts reaction.

• NitrationNarrower topic: The nitronium ion acts as the electrophile in common aromatic nitrations.

• Retrosynthetic analysisRelated: A complementary electrophilic fragment helps convert a disconnection into a plausible reaction pair.

• AlkylationNarrower topic: Alkyl donors commonly act as electrophiles at the carbon being transferred.

• Protecting groupRelated: Protection can prevent electrophiles from reacting with a functional group.

• Friedel–Crafts acylationNarrower topic: The reaction’s central mechanistic idea is an electrophile attacking an aromatic ring.

• TRPA1Related: Electrophiles activate TRPA1 through covalent reactions, but this mechanism cannot explain every reported stimulus.

• EpoxideRelated: Epoxide carbons act as electrophilic sites in many ring-opening reactions.

• Allyl isothiocyanateRelated: The central carbon of the isothiocyanate group reacts with nucleophiles.

• Hydride transferRelated: Many hydride acceptors are electrophilic centers, especially polarized carbonyl carbons.

• Carbonyl compoundRelated: The polarized carbonyl carbon behaves as an electrophilic site.

• Acyl groupNarrower topic: The acyl carbon behaves as an electrophilic site because the carbonyl polarizes its bond.

• Addition reactionRelated: Electrophiles initiate many additions to electron-rich carbon–carbon double bonds.

• Organic reactionRelated: Electrophiles receive electron density from nucleophiles and other donors.

• Electrophilic substitutionNarrower topic: Its attack on the aromatic ring initiates the substitution pathway.

• George Andrew OlahNarrower topic: Carbocations are powerful electrophiles, linking Olah’s subject to a broad reaction principle.

• Lewis acids and basesRelated: Electrophiles commonly behave as Lewis acids in organic reactions.

• Non-nucleophilic baseRelated: Electrophiles are the targets these bases are selected not to attack.

• ReagentRelated: Electrophilic reagents accept electron density to make or break bonds.