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  2. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol reacts with dilute nitric acid at room temperature to give a mixture of 2-nitrophenol and 4-nitrophenol while with concentrated nitric acid, additional nitro groups are introduced, e.g. to give 2,4,6-trinitrophenol. Friedel Crafts alkylations of phenol and its derivatives often proceed without catalysts. Alkylating agents include alkyl ...

  3. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  4. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.

  5. Phenol formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Phenol_formaldehyde_resin

    Phenolic resins are also used for making exterior plywood commonly known as weather and boil proof (WBP) plywood because phenolic resins have no melting point but only a decomposing point in the temperature zone of 220 °C (428 °F) and above. Phenolic resin is used as a binder in loudspeaker driver suspension components which are made of cloth.

  6. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    Phenol is readily alkylated at the ortho positions using alkenes in the presence of a Lewis acid such as aluminium phenoxide: [citation needed] CH 2 =CR 2 + C 6 H 5 OH → R 2 CHCH 2 -2-C 6 H 4 OH More than 100,000 tons of tert-butyl phenols are produced annually (year: 2000) in this way, using isobutylene (CH 2 =CMe 2 ) as the alkylating agent.

  7. Bakelite - Wikipedia

    en.wikipedia.org/wiki/Bakelite

    Bakelite was produced for the first time in 1872 by Adolf von Baeyer, though its use as a commercial product was not considered at the time. [6]Leo Baekeland was already wealthy due to his invention of Velox photographic paper when he began to investigate the reactions of phenol and formaldehyde in his home laboratory.

  8. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    Another method entails methylation of phenol with methanol over a solid acid catalyst, often comprising magnesium oxide or alumina. Temperatures above 300 °C are typical. Anisole converts to cresols under these conditions. [5] [6] Another isomer of cresol is called Benzyl alcohol, or alpha-cresol (α-cresol).

  9. Picric acid - Wikipedia

    en.wikipedia.org/wiki/Picric_acid

    Melting point: 122.5 °C (252.5 °F; 395.6 K) ... phenol was obtained from coal as a co-product of coke ovens and the manufacture of gas ... and careful temperature ...