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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.
In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group (−C(=O)−OH) [1] attached to an R-group. The general formula of a carboxylic acid is often written as R−COOH or R−CO 2 H, sometimes as R−C(O)OH with R referring to an organyl group (e.g., alkyl, alkenyl, aryl), or hydrogen, or other groups ...
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 acid CH 3 (CH 2) 6 COOH C8:0 Pelargonic acid: Nonanoic acid CH 3 (CH 2) 7 COOH C9:0 Capric acid: Decanoic acid CH 3 (CH 2) 8 COOH C10:0 Undecylic acid: Undecanoic ...
Pages in category "Carboxylic acids" The following 200 pages are in this category, out of approximately 448 total. This list may not reflect recent changes.
Ricinoleic acid (12-hydroxy-9-cis-octadecenoic acid)), a major component of the seed oil obtained from castor plant; Common amino acids: Serine (2-amino-3-hydroxypropanoic acid), HOCH 2 CH(NH 2)CO 2 H; Threonine; Tyrosine, 4−HOC 6 H 4 CH 2 CH(NH 2)CO 2 H; Aldonic acids are sugar acids with the general chemical formula, HO 2 C(CHOH) n CH 2 OH.
A tricarboxylic acid is an organic carboxylic acid whose chemical structure contains three carboxyl functional groups (−COOH). The best-known example of a tricarboxylic acid is citric acid . Uses
An organic acid is an organic compound with acidic properties. 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.
Propane-1,2,3-tricarboxylic acid is well suited to bind to aconitase as it only lacks the hydroxyl group in comparison to citric acid. However, the hydroxyl group is essential to proceed from citric acid to aconitic acid; therefore, the enzyme is not able to complete the reaction with propane-1,2,3-tricarboxylic acid.