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Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...
To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...
An example of a common name is terpineol, the name of which can tell us only that it is an alcohol (because the suffix "-ol" is in the name) and it should then have a hydroxyl group (–OH) attached to it. The IUPAC naming system for organic compounds can be demonstrated using the example provided in the adjacent image.
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.
Names Preferred IUPAC name. Cyclohexylmethanol. Other names ... It is a cyclohexane ring functionalized with an alcohol, specifically a hydroxymethyl group. The ...
Names Preferred IUPAC name. ... It is the carboxylic acid of cyclohexane. It is a colorless oil that crystallizes near room temperature. [2] Preparation and reactions
Names Preferred IUPAC name. Cyclohexanethiol. ... It was first prepared by the free-radical reaction of cyclohexane using carbon disulfide as a sulfur source. [1]
The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source and follow its directions.