Linked from

The 16 pages that link to Dicarboxylic acid, each with the reason it gives.

• PolyesterRelated: Dicarboxylic acids commonly provide the acid-derived units in polyester synthesis.

• PolycondensationRelated: Dicarboxylic acids supply one common pair of condensation sites for polyester and polyamide synthesis.

• Adipic acidNarrower topic: Adipic acid’s two terminal carboxyl groups define its characteristic reaction pattern.

• Tartaric acidNarrower topic: Tartaric acid belongs to this class because its molecule has two carboxyl groups.

• Malic acidNarrower topic: Malic acid's two carboxyl groups account for its dibasic acidity.

• Oxalic acidNarrower topic: Oxalic acid is the smallest member of this structural family.

• Succinic acidNarrower topic: Succinic acid belongs to this class, with one carboxyl group at each end.

• MalateNarrower topic: Malic acid has two carboxyl groups, which can lose protons to form malate.

• Malonic acidNarrower topic: This class describes malonic acid's defining functional-group arrangement.

• Fumaric acidNarrower topic: Fumaric acid’s two carboxyl groups define its acidic character and salt-forming reactions.

• Azelaic acidNarrower topic: Azelaic acid belongs to this structural family, with carboxyl groups at both ends.

• Methylmalonic acidNarrower topic: Methylmalonic acid belongs to this chemical class because it contains two carboxyl groups.

• Glutaric acidNarrower topic: Glutaric acid belongs to this family because each end of its carbon chain carries a carboxyl group.

• Alpha-ketoglutaric acidNarrower topic: Its two carboxyl groups give alpha-ketoglutarate its acidic, charged character in cells.

• Oxaloacetic acidNarrower topic: Oxaloacetic acid has two carboxyl groups, giving it its acidic character.

• Pimelic acidNarrower topic: Pimelic acid belongs to this class, with carboxyl groups at both ends of its chain.