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  2. Naphthalene - Wikipedia

    en.wikipedia.org/wiki/Naphthalene

    Naphthalene is an organic compound with formula C 10 H 8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. [15] As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings.

  3. 1,4-Naphthoquinone - Wikipedia

    en.wikipedia.org/wiki/1,4-Naphthoquinone

    1,4-Naphthoquinone or para-naphthoquinone is a quinone derived from naphthalene. It forms volatile yellow triclinic crystals and has a sharp odor similar to benzoquinone. It is almost insoluble in cold water, slightly soluble in petroleum ether, and more soluble in polar organic solvents. In alkaline solutions it produces a reddish-brown color ...

  4. Sodium naphthalene - Wikipedia

    en.wikipedia.org/wiki/Sodium_naphthalene

    Sodium naphthalene is an organic salt with the chemical formula Na + [C 10 H 8] −. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na +. [1]

  5. Polychlorinated naphthalene - Wikipedia

    en.wikipedia.org/wiki/Polychlorinated_naphthalene

    Structure of 2,3,6,7-Tetrachloronaphthalene. Polychlorinated naphthalene (PCN) are the products obtained upon treatment of naphthalene with chlorine. The generic chemical formula is C 10 H 8−(m+n) Cl (m+n). Commercial PCNs are mixtures of up to 75 components and byproducts. [1] The material is an oil or a waxy solid, depending on the degree ...

  6. 1,8-Bis (dimethylamino)naphthalene - Wikipedia

    en.wikipedia.org/wiki/1,8-Bis(dimethylamino...

    With a pK a of 12.34 [4] for its conjugate acid in aqueous solution, 1,8-bis(dimethylamino)naphthalene is one of the strongest organic bases. However, it only absorbs protons slowly—hence the trade name. The high basicity is attributed to the relief of strain upon protonation and/or the strong interaction between the nitrogen lone pairs. [3]

  7. Sodium compounds - Wikipedia

    en.wikipedia.org/wiki/Sodium_compounds

    The structure of sodium chloride, showing octahedral coordination around Na + and Cl − centres. This framework disintegrates when dissolved in water and reassembles when the water evaporates. Sodium compounds are of immense commercial importance, being particularly central to industries producing glass, paper, soap, and textiles. [6]

  8. Naphthoquinone - Wikipedia

    en.wikipedia.org/wiki/Naphthoquinone

    Chemical structure of 1,4-naphthoquinone. Naphthoquinones constitute a class of organic compounds structurally related to naphthalene. Two isomers are common for the parent naphthoquinones: 1,2-Naphthoquinone; 1,4-Naphthoquinone

  9. 1-Naphthol - Wikipedia

    en.wikipedia.org/wiki/1-naphthol

    1-Naphthol, or α-naphthol, is an organic compound with the formula C 10 H 7 OH. It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol. Both isomers are soluble in simple organic solvents. They are ...