enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Dibromophenol - Wikipedia

    en.wikipedia.org/wiki/Dibromophenol

    There are six structural isomers, each with the molecular formula C 6 H 4 Br 2 O, ... 3,5-Dibromophenol, 1,3-Dibromo-5-hydroxybenzene Structural formula: CAS Number:

  3. 2,4-Dibromophenol - Wikipedia

    en.wikipedia.org/wiki/2,4-Dibromophenol

    At room temperature, 2,4-dibromophenol is a solid with needle-like crystals. It melts at 38 °C (100.4 °F) and boils at 238.5 °C (461.3 °F). it has a molecular weight of 251.905 g/mol. It is soluble in water, ethanol, ether and benzene and slightly soluble in carbon tetrachloride. [1]

  4. Bromophenol - Wikipedia

    en.wikipedia.org/wiki/Bromophenol

    Monobromrophenols have three isomers because there is only one bromine atom that can occupy one of three ring positions on the phenol molecule; 2-bromophenol, for example, is the isomer that has a bromine atom in the ortho position.

  5. List of inorganic compounds - Wikipedia

    en.wikipedia.org/wiki/List_of_inorganic_compounds

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  6. Monobromophenol - Wikipedia

    en.wikipedia.org/wiki/Monobromophenol

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  7. Valence isomer - Wikipedia

    en.wikipedia.org/wiki/Valence_isomer

    In organic chemistry, two molecules are valence isomers when they are constitutional isomers that can interconvert through pericyclic reactions. [1] [2] Benzene

  8. Discover the best free online games at AOL.com - Play board, card, casino, puzzle and many more online games while chatting with others in real-time.

  9. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    All three isomers have the chemical formula C 6 H 6 O 2. Similar to other phenols, the hydroxyl groups on the aromatic ring of a benzenediol are weakly acidic . Each benzenediol can lose an H + from one of the hydroxyls to form a type of phenolate ion.