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Download as PDF; Printable version; In other projects ... 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 ...
Download QR code; Print/export Download as PDF; Printable version; In other projects Appearance. move to sidebar hide. From Wikipedia, the free encyclopedia. Redirect ...
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.
youtube-dl is a free and open source software tool for downloading video and audio from YouTube [3] and over 1,000 other video hosting websites. [4] It is released under the Unlicense software license. [5] As of September 2021, youtube-dl is one of the most starred projects on GitHub, with over 100,000 stars. [6]
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.
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'.