Nucleophilic aromatic substitution
id:
nucleophilic-aromatic-substitution-162-12892566
title:
Nucleophilic aromatic substitution
text:
A nucleophilic aromatic substitution (SNAr) is a substitution reaction in organic chemistry in which the nucleophile displaces a good leaving group, such as a halide, on an aromatic ring. Aromatic rings are usually nucleophilic, but some aromatic compounds do undergo nucleophilic substitution. Just as normally nucleophilic alkenes can be made to undergo conjugate substitution if they carry electron-withdrawing substituents, so normally nucleophilic aromatic rings also become electrophilic if the
brand slug:
wiki
category slug:
encyclopedia
description:
Chemical reaction mechanism
original url:
https://en.wikipedia.org/wiki/Nucleophilic_aromatic_substitution
date created:
2005-08-08T21:08:41Z
date modified:
2024-08-28T12:42:32Z
main entity:
{"identifier":"Q901713","url":"https://www.wikidata.org/entity/Q901713"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/6/66/Aromatic_nucleophilic_substitution.svg","width":600,"height":300}
fields total:
13
integrity:
16