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2-Hexanol (hexan-2-ol) is a six-carbon alcohol in which the hydroxy group (OH) is located on the second carbon atom. Its chemical formula is C 6 H 14 O or C 6 H 13 OH. It is an isomer of the other hexanols. 2-Hexanol has a chiral center and can be resolved into two different enantiomers. Its toxicity is based on metabolism to hexane-2,5-dione. [3]
The following other wikis use this file: Usage on azb.wikipedia.org ۲-هقزانول; Usage on fa.wikipedia.org ۲-هگزانول; Usage on fi.wikipedia.org 2-heksanoli; Usage on fr.wikipedia.org 2-Hexanol; Usage on hu.wikipedia.org 2-Hexanol; Usage on id.wikipedia.org 2-Heksanol; Usage on ja.wikipedia.org 2-ヘキサノール; Usage on pt ...
Cyclohexanol is the organic compound with the formula HOCH(CH 2) 5.The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group. [4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature.
Cyclohexane-1,2,3,4,5,6-hexol is a family of chemical compounds with formula C 6 H 12 O 6, whose molecule consists of a ring of six carbon atoms, each bound to one hydrogen atom and one hydroxyl group (–OH). There are nine stereoisomers, that differ by the position of the hydroxyl groups relative to the mean plane of the ring.
Hexanol may refer to any of the following isomeric organic compounds with the formula C 6 H 13 OH: Structure Type IUPAC name Boiling point (°C)
[1] [2] Some commercially important fatty alcohols are lauryl, stearyl, and oleyl alcohols. They are colourless oily liquids (for smaller carbon numbers) or waxy solids, although impure samples may appear yellow. Fatty alcohols usually have an even number of carbon atoms and a single alcohol group (–OH) attached to the terminal carbon. Some ...
[2] Through a variety of mechanisms, the removal of a hydride equivalent converts a primary or secondary alcohol to an aldehyde or ketone, respectively. The oxidation of primary alcohols to carboxylic acids normally proceeds via the corresponding aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH) 2) by reaction with ...
Hexanol may refer to any isomeric organic compounds with the formula C 6 H 13 OH: Pages in category "Hexanols" The following 17 pages are in this category, out of 17 total.