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  2. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    A molecule is composed of one or more chemical bonds between molecular orbitals of different atoms. A molecule may be polar either as a result of polar bonds due to differences in electronegativity as described above, or as a result of an asymmetric arrangement of nonpolar covalent bonds and non-bonding pairs of electrons known as a full ...

  3. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    Specifically, the dipole can cause electrostatic attraction or repulsion of the electrons from the non-polar molecule, depending on orientation of the incoming dipole. [13] Atoms with larger atomic radii are considered more "polarizable" and therefore experience greater attractions as a result of the Debye force. [citation needed]

  4. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone ( >C=O ). It is a colorless, highly volatile , and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops .

  5. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    The simplest class have the formula (CH 2) n CO, where n varies from 2 for cyclopropanone ((CH 2) 2 CO) to the tens. Larger derivatives exist. Larger derivatives exist. Cyclohexanone ( (CH 2 ) 5 CO ), a symmetrical cyclic ketone, is an important intermediate in the production of nylon .

  6. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    Propene and benzene are converted to acetone and phenol via the cumene process. Overview of the cumene process. Propene is also used to produce isopropyl alcohol (propan-2-ol), acrylonitrile, propylene oxide, and epichlorohydrin. [18] The industrial production of acrylic acid involves the catalytic partial oxidation of propene. [19]

  7. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    The two tautomeric forms can be distinguished by NMR spectroscopy, IR spectroscopy and other methods. [5] [6] The equilibrium constant tends to be high in nonpolar solvents; when K keto→enol is equal or greater than 1, the enol form is favoured. The keto form becomes more favourable in polar, hydrogen-bonding solvents, such as water. [7]

  8. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde, ketone, or carboxylic acid), then the prefix hydroxy-is used, [19] e.g., as in 1-hydroxy-2-propanone (CH ...

  9. Reversed-phase chromatography - Wikipedia

    en.wikipedia.org/wiki/Reversed-phase_chromatography

    Reversed-phase liquid chromatography (RP-LC) is a mode of liquid chromatography in which non-polar stationary phase and polar mobile phases are used for the separation of organic compounds. [ 1 ] [ 2 ] [ 3 ] The vast majority of separations and analyses using high-performance liquid chromatography (HPLC) in recent years are done using the ...