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  2. Biphenyl - Wikipedia

    en.wikipedia.org/wiki/Biphenyl

    Biphenyl (also known as diphenyl, phenylbenzene, 1,1′-biphenyl, lemonene [4] or BP) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl .

  3. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    The polarity, dipole moment, polarizability and hydrogen bonding of a solvent determines what type of compounds it is able to dissolve and with what other solvents or liquid compounds it is miscible. Generally, polar solvents dissolve polar compounds best and non-polar solvents dissolve non-polar compounds best; hence "like dissolves like".

  4. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  5. 4,4'-Biphenol - Wikipedia

    en.wikipedia.org/wiki/4,4'-Biphenol

    The industrial synthesis of 4,4′-biphenol was developed by Allan Hay in the 1960s. [2] [3] As the direct oxidative coupling of phenol gives a mixture of isomers, [4] [5] 4,4′-biphenol is instead prepared from 2,6-di-tert-butylphenol, where para-coupling is the only possibility. [3]

  6. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    Polar molecules must contain one or more polar bonds due to a difference in electronegativity between the bonded atoms. Molecules containing polar bonds have no molecular polarity if the bond dipoles cancel each other out by symmetry. Polar molecules interact through dipole-dipole intermolecular forces and hydrogen bonds.

  7. Polychlorinated biphenyl - Wikipedia

    en.wikipedia.org/wiki/Polychlorinated_biphenyl

    In PCBs, some of the hydrogen atoms in biphenyl are replaced by chlorine atoms. There are 209 different chemical compounds in which one to ten chlorine atoms can replace hydrogen atoms. PCBs are typically used as mixtures of compounds and are given the single identifying CAS number 1336-36-3. About 130 different individual PCBs are found in ...

  8. Biphenol - Wikipedia

    en.wikipedia.org/wiki/Biphenol

    Download as PDF; Printable version; In other projects ... In organic chemistry, a biphenol refers to compounds with the formula (C 6 H 4 OH) 2. Such compounds ...

  9. Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A

    Bisphenol A (BPA) is a chemical compound primarily used in the manufacturing of various plastics. It is a colourless solid which is soluble in most common organic solvents, but has very poor solubility in water. [2] [7] BPA is produced on an industrial scale by the condensation reaction of phenol and acetone. Global production in 2022 was ...