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The resulting cyclohexanecarboxaldehyde is then hydrogenated to give the alcohol. [5] [6] References
cyclohexanecarboxaldehyde: 2043-61-0 C 7 H 12 O: dicyclopropyl carbinol: 14300-33-5 C 7 H 12 O: methycyclohexanone: 1331-22-2 C 7 H 12 O 2: cyclohexanecarboxylic acid: 98-89-5 C 7 H 12 O 2: cyclopentaneacetic acid: 1123-00-8 C 7 H 12 O 2: ethyl cyclobutanecarboxylate: 14924-53-9 C 7 H 12 O 2: ethyl tiglate: 5837-78-5 C 7 H 12 O 2 ...
Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.
The naming of polycyclic alkanes is more complex, with the base name indicating the number of carbons in the ring system, a prefix indicating the number of rings (e.g., "bicyclo"), and a numeric prefix before that indicating the number of carbons in each part of each ring, exclusive of vertices.
Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 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.
Typical synthesis starts from myrcene [2] and involves a Diels–Alder reaction with acrolein to produce the cyclohexenecarbaldehyde group, this species is marketed as a fragrance in its own right, most commonly under the name 'myrac aldehyde'.
It is prepared by hydrogenation of benzoic acid.. Cyclohexanecarboxylic acid is a precursor to the nylon-6 precursor caprolactam via its reaction with nitrosylsulfuric acid. ...
Cyclohexane is a cycloalkane with the molecular formula C 6 H 12.Cyclohexane is non-polar.Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used).