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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...

    Solvent. Density (g cm-3) Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source. Aniline. 184.3.

  4. Bakelite - Wikipedia

    en.wikipedia.org/wiki/Bakelite

    Bakelite (/ ˈbeɪkəlaɪt / BAY-kə-lyte), formally poly­oxy­benzyl­methylene­glycol­anhydride, is a thermosetting phenol formaldehyde resin, formed from a condensation reaction of phenol with formaldehyde. The first plastic made from synthetic components, it was developed by Leo Baekeland in Yonkers, New York, in 1907, and patented on ...

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

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

    1802 K. 1529 °C. 2784 °F. 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.

  7. 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).

  8. 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.

  9. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    Melting point: 122 °C (252 °F ... temperature. 571 °C (1,060 °F; ... The phenol can be converted to cyclohexanol, which is a starting material for nylon synthesis.