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  2. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  3. Dicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Dicarboxylic_acid

    In organic chemistry, a dicarboxylic acid is an organic compound containing two carboxyl groups (−COOH). The general molecular formula for dicarboxylic acids can be written as HO 2 C−R−CO 2 H, where R can be aliphatic or aromatic. In general, dicarboxylic acids show similar chemical behavior and reactivity to monocarboxylic acids.

  4. Phosphorous acid - Wikipedia

    en.wikipedia.org/wiki/Phosphorous_acid

    This acid is diprotic (readily ionizes two protons), not triprotic as might be suggested by this formula. Phosphorous acid is an intermediate in the preparation of other phosphorus compounds. Organic derivatives of phosphorous acid, compounds with the formula RPO 3 H 2, are called phosphonic acids.

  5. Disodium hydrogen arsenate - Wikipedia

    en.wikipedia.org/wiki/Disodium_hydrogen_arsenate

    Disodium hydrogen arsenate is highly toxic. The salt is the conjugate base of arsenic acid. It is a white, water-soluble solid. [1] Being a diprotic acid, its acid-base properties is described by two equilibria: H 2 AsO − 4 + H 2 O ⇌ HAsO 2− 4 + H 3 O + (pK a2 = 6.94) HAsO 2− 4 + H 2 O ⇌ AsO 3− 4 + H 3 O + (pK a3 = 11.5)

  6. List of saturated fatty acids - Wikipedia

    en.wikipedia.org/wiki/List_of_saturated_fatty_acids

    Common Name Systematic Name Structural Formula Lipid Numbers Propionic acid: Propanoic acid CH 3 CH 2 COOH C3:0 Butyric acid: Butanoic acid CH 3 (CH 2) 2 COOH C4:0 Valeric acid: Pentanoic acid CH 3 (CH 2) 3 COOH C5:0 Caproic acid: Hexanoic acid CH 3 (CH 2) 4 COOH C6:0 Enanthic acid: Heptanoic acid CH 3 (CH 2) 5 COOH C7:0 Caprylic acid: Octanoic ...

  7. Malonic acid - Wikipedia

    en.wikipedia.org/wiki/Malonic_acid

    The fluorinated version of malonic acid is difluoromalonic acid. Chemical structure of the malonate dianion. Malonic acid is diprotic; that is, it can donate two protons per molecule. Its first is 2.8 and the second is 5.7. [2] Thus the malonate ion can be H OOCCH 2 COO − or C H 2 (COO) 2− 2.

  8. Selenous acid - Wikipedia

    en.wikipedia.org/wiki/Selenous_acid

    Selenous acid is analogous to sulfurous acid, but it is more readily isolated. Selenous acid is easily formed upon the addition of selenium dioxide to water. As a crystalline solid, the compound can be seen as pyramidal molecules that are interconnected with hydrogen bonds. In solution it is a diprotic acid: [3] H 2 SeO 3 ⇌ H + + HSeO − 3 ...

  9. Tartaric acid - Wikipedia

    en.wikipedia.org/wiki/Tartaric_acid

    The acid itself is added to foods as an antioxidant E334 and to impart its distinctive sour taste. Naturally occurring tartaric acid is a useful raw material in organic chemical synthesis. Tartaric acid, an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics and is a dihydroxyl derivative of succinic acid.