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  2. Organic acid - Wikipedia

    en.wikipedia.org/wiki/Organic_acid

    The most common organic acids are the carboxylic acids, whose acidity is associated with their carboxyl group –COOH. Sulfonic acids, containing the group –SO 2 OH, are relatively stronger acids. Alcohols, with –OH, can act as acids but they are usually very weak. The relative stability of the conjugate base of

  3. Organic base - Wikipedia

    en.wikipedia.org/wiki/Organic_base

    An organic base is an organic compound which acts as a base. Organic bases are usually, but not always, proton acceptors. They usually contain nitrogen atoms, which can easily be protonated. For example, amines or nitrogen-containing heterocyclic compounds have a lone pair of electrons on the nitrogen atom and can thus act as proton acceptors. [1]

  4. 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.

  5. Category:Acids - Wikipedia

    en.wikipedia.org/wiki/Category:Acids

    Pages in category "Acids" The following 35 pages are in this category, out of 35 total. ... Lewis acids and bases; List of acids by Hammett acidity; Lyonium ion; N ...

  6. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Ionization and Brønsted character of N-terminal amino, C-terminal carboxylate, and side chains of amino acid residues. The common natural forms of amino acids have a zwitterionic structure, with −NH + 3 (−NH + 2 − in the case of proline) and −CO − 2 functional groups attached to the same C atom, and are thus α-amino acids, and are ...

  7. Base (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Base_(chemistry)

    According to the original formulation of Lewis, when a neutral base forms a bond with a neutral acid, a condition of electric stress occurs. [7] The acid and the base share the electron pair that formerly belonged to the base. [7] As a result, a high dipole moment is created, which can only be decreased to zero by rearranging the molecules. [7]

  8. List of acids by Hammett acidity - Wikipedia

    en.wikipedia.org/wiki/List_of_acids_by_hammett...

    List of acids by Hammett acidity Name Hammett acidity Ref Trifluoroacetic acid-2.7 [1] Phosphoric acid-4.66 [2] Nitric acid-6.3 [3] Methanesulfonic acid-7.86 [2]

  9. Nucleoside - Wikipedia

    en.wikipedia.org/wiki/Nucleoside

    Nucleosides are glycosylamines that can be thought of as nucleotides without a phosphate group.A nucleoside consists simply of a nucleobase (also termed a nitrogenous base) and a five-carbon sugar (ribose or 2'-deoxyribose) whereas a nucleotide is composed of a nucleobase, a five-carbon sugar, and one or more phosphate groups.