Linked from

The 11 pages that link to Enol, each with the reason it gives.

• Hydroxyl groupBroader topic: Enols show how the hydroxyl group’s neighboring bonds alter its reactivity.

• KetoneRelated: Ketones can interconvert with enols through keto–enol tautomerism.

• DecarboxylationRelated: Many β-keto acid decarboxylations first form an enol, which then tautomerizes.

• ThiolCompared with: Enols provide an oxygen-based comparison for sulfur-containing thiol tautomers.

• TautomerismBroader topic: Enols are one structural form in keto–enol tautomerism.

• EnolateCompared with: Enols are neutral tautomers related to enolates by protonation.

• Aldol reactionRelated: It is the neutral tautomer that can act as the nucleophile in acid-catalyzed aldol reactions.

• Keto–enol tautomerismBroader topic: It is the specific product form paired with the keto form.

• CyclohexanoneRelated: Cyclohexanone can reversibly form its enol through keto–enol tautomerism.

• TautomerBroader topic: An enol is one member of a keto–enol tautomeric pair.

• Vinyl alcoholNarrower topic: Vinyl alcohol is the simplest enol, with only two carbon atoms.