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  2. Ammonium - Wikipedia

    en.wikipedia.org/wiki/Ammonium

    The hydrogen atoms in the ammonium ion can be substituted with an alkyl group or some other organic group to form a substituted ammonium ion (IUPAC nomenclature: aminium ion). Depending on the number of organic groups, the ammonium cation is called a primary , secondary , tertiary , or quaternary .

  3. Alkylammonium - Wikipedia

    en.wikipedia.org/wiki/Alkylammonium

    In organic chemistry, alkylammonium refers to cations of the formula [R 4−n NH n] +, where R = alkyl and 1≤ n ≤ 4. The cations with four alkyl substituents, i.e., [R 4 N] +, are further classified as quaternary ammonium cations and are discussed more thoroughly in the article with that title.

  4. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −C n H 2n−1. [2] Typically an alkyl is a part of a larger molecule. In structural formulae, the symbol R is used to designate a generic (unspecified) alkyl group. The smallest alkyl group is methyl, with the formula −CH 3 ...

  5. Ammonium hypoiodite - Wikipedia

    en.wikipedia.org/wiki/Ammonium_hypoiodite

    Ammonium hypoiodites are a class of reactive intermediates used in certain organic oxidation reactions. They consist of either ammonium itself or an alkylammonium with various substituents as cation , paired with a hypoiodite anion as the active oxidant .

  6. Quaternary ammonium cation - Wikipedia

    en.wikipedia.org/wiki/Quaternary_ammonium_cation

    Quaternary ammonium cation. The R groups may be the same or different alkyl or aryl groups. Also, the R groups may be connected. In organic chemistry, quaternary ammonium cations, also known as quats, are positively-charged polyatomic ions of the structure [NR 4] +, where R is an alkyl group, an aryl group [1] or organyl group.

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The alkyl (R') group is named first. The R−C(=O)O part is then named as a separate word based on the carboxylic acid name, with the ending changed from "-oic acid" to "-oate" or "-carboxylate" For example, CH 3 CH 2 CH 2 CH 2 COOCH 3 is methyl pentanoate, and (CH 3) 2 CHCH 2 CH 2 COOCH 2 CH 3 is ethyl 4-methylpentanoate.

  8. Category:Alkyl groups - Wikipedia

    en.wikipedia.org/wiki/Category:Alkyl_groups

    Alkyl groups are saturated hydrocarbons substituents with the general formula C n H 2n+1 See also: Category:Alkyl compounds Wikimedia Commons has media related to Alkyl groups .

  9. Metal ammine complex - Wikipedia

    en.wikipedia.org/wiki/Metal_ammine_complex

    This name has been discarded as modern chemistry considers color less important than molecular structure. Other metal ammine complexes also were labeled according to their color, such as purpureo (Latin: purple) for a cobalt pentammine complex , and praseo (Greek: green) and violeo (Latin: violet) for two isomeric tetrammine complexes.