Electrophile

In chemistry, an electrophile is a chemical species that forms bonds with nucleophiles by accepting an electron pair.[1] Because electrophiles accept electrons, they are Lewis acids.[2] Most electrophiles are positively charged, have an atom that carries a partial positive charge, or have an atom that does not have an octet of electrons.

Electrophiles mainly interact with nucleophiles through addition and substitution reactions. Frequently seen electrophiles in organic syntheses include cations such as H+ and NO+, polarized neutral molecules such as HCl, alkyl halides, acyl halides, and carbonyl compounds, polarizable neutral molecules such as Cl2 and Br2, oxidizing agents such as organic peracids, chemical species that do not satisfy the octet rule such as carbenes and radicals, and some Lewis acids such as BH3 and DIBAL.

  1. ^ "Nucleophiles and Electrophiles". butane.chem.uiuc.edu. Archived from the original on 2020-08-01. Retrieved 2020-09-21.
  2. ^ "Electrophile | chemistry". Encyclopedia Britannica. Retrieved 2020-09-21.

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