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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 .
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.
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 ...
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 .
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.
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.
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 .
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.