Linked from

The 13 pages that link to Carboxylate, each with the reason it gives.

• Carboxylic acidBroader topic: Loss of the acidic proton converts a carboxylic acid into this resonance-stabilized form.

• SoapRelated: The charged carboxylate head gives common soaps their water-attracting end.

• SaponificationRelated: The fatty-acid products are carboxylates paired with metal cations.

• Carboxyl groupBroader topic: Deprotonation converts the group into its resonance-stabilized, negatively charged form.

• Dicarboxylic acidRelated: Each carboxyl group can form a carboxylate, often with a distinct ionization state.

• AcetateNarrower topic: Acetate is the simplest widely encountered example of a carboxylate.

• CitrateNarrower topic: Citrate’s three carboxyl groups account for much of its negative charge.

• Sodium acetateNarrower topic: Acetate is a carboxylate, the anionic part of sodium acetate.

• Oxidation of aldehydesRelated: Basic reaction conditions commonly leave the oxidation product in this ionic form.

• Potassium sorbateRelated: The sorbate ion is the carboxylate form of sorbic acid.

• Haloform reactionRelated: The acyl fragment remains as a carboxylate under basic conditions.

• Pimelic acidRelated: Deprotonation converts pimelic acid’s terminal carboxyl groups into carboxylates.

• Sodium formateNarrower topic: Formate is the smallest carboxylate, defining sodium formate’s anion.