Linked from

The 62 pages that link to Nucleophilic substitution, each with the reason it gives.

• ThiolNarrower topic: Thiolate ions act as nucleophiles in substitution reactions that form thioethers.

• EtherNarrower topic: Williamson synthesis forms ethers through nucleophilic substitution at an alkyl carbon.

• SN2 reactionNarrower topic: SN2 is one of the two principal pathways for nucleophilic substitution.

• SN1 reactionNarrower topic: SN1 is one mechanistic pathway within this broader reaction class.

• N-alkylationNarrower topic: Alkyl halides commonly undergo substitution when nitrogen attacks their carbon atom.

• SNi reactionNarrower topic: SNi is one mechanistic pathway within this broader reaction family.

• Allylic rearrangementNarrower topic: Allylic rearrangement is a distinctive form of substitution with a shifted bonding position.

• Benzyl chlorideNarrower topic: Nucleophiles displace chloride from its activated benzylic carbon.

• BromoethaneNarrower topic: Nucleophiles displace bromide from bromoethane to form new carbon–nitrogen, carbon–oxygen, and carbon–carbon bonds.

• IodomethaneNarrower topic: Nucleophiles commonly displace iodide from iodomethane in carbon–carbon bond-forming reactions.