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Cyclohexanecarboxylic acid is a precursor to the nylon-6 precursor caprolactam via its reaction with nitrosylsulfuric acid. It can also be oxidized to cyclohexene. [2] Cyclohexanecarboxylic acid exhibits the reactions typical of carboxylic acids, including its conversion to the acid chloride cyclohexanecarbonyl chloride. [3] [4]
When comparing a polar and nonpolar molecule with similar molar masses, the polar molecule in general has a higher boiling point, because the dipole–dipole interaction between polar molecules results in stronger intermolecular attractions. One common form of polar interaction is the hydrogen bond, which is also known as the H-bond.
Cyclohexane is considered nonpolar, meaning that there is no electronegative difference between its bonds and its overall structure is symmetrical. Due to this, when cyclohexane is immersed in a polar solvent, it will have less solvent distribution, which signifies a poor interaction between the solvent and solute.
The molecular formula C 7 H 12 O 2 may refer to: Butyl acrylate; Cyclohexanecarboxylic acid; trans-3-Methyl-2-hexenoic acid (TMHA)
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
Pages for logged out editors learn more. Contributions; Talk; Cyclohexanecarboxylic acids
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). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5]
Pages in category "Cyclohexanecarboxylic acids" The following 7 pages are in this category, out of 7 total. This list may not reflect recent changes. ...