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  2. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    The resulting cyclohexanecarboxaldehyde is then hydrogenated to give the alcohol. [5] [6] References

  3. Hydroxyisohexyl 3-cyclohexene carboxaldehyde - Wikipedia

    en.wikipedia.org/?title=Hydroxyisohexyl_3...

    This page was last edited on 23 February 2012, at 18:26 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  4. Alkyl cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Alkyl_cycloalkane

    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.

  5. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    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.

  6. Hydroxymethylpentylcyclohexenecarboxaldehyde - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethylpentylcyclo...

    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'.

  7. Cyclohexanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanecarboxylic_acid

    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. ...

  8. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7]Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam.

  9. Hydroformylation - Wikipedia

    en.wikipedia.org/wiki/Hydroformylation

    Hydroformylation of an alkene (R 1 to R 3 organyl groups (i. e. alkyl-or aryl group) or hydrogen). In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from alkenes (R 2 C=CR 2).