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2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid. The oxidation involves radicals and the intermediacy of the hydroperoxide C 6 H 11 O 2 H. Alternatively, cyclohexanol can be produced by the hydrogenation of phenol ...
2-Hexanone (methyl butyl ketone, MBK) is a ketone used as a general solvent and in paints. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins.
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]
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.
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Commas are put between numbers (2 5 5 becomes 2,5,5) Hyphens are put between a number and a letter (2 5 5 trimethylheptane becomes 2,5,5-trimethylheptane) Successive words are merged into one word (trimethyl heptane becomes trimethylheptane) Note: IUPAC uses one-word names throughout. This is why all parts are connected. The resulting name ...
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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) Primary Hexan-1-ol ...