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The resulting cyclohexanecarboxaldehyde is then hydrogenated to give the alcohol. [5] [6] References
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. ...
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Ferrocenecarboxaldehyde behaves like other aldehydes in terms of its reactivity, the main difference is that it is electroactive. Its basicity is indicated by the solubility of the compound in hydrochloric acid.
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.
They are named analogously to their normal alkane counterpart of the same carbon count: methylcyclopropane, methylcyclobutane, methylcyclopentane, methylcyclohexane, etc. [1] Methylcycloalkanes are classed into compounds with small, normal and bigger cycloalkanes, where cyclopropane and cyclobutane are the small ones, cyclopentane , cyclohexane ...
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'.
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).