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  2. Iron compounds - Wikipedia

    en.wikipedia.org/wiki/Iron_compounds

    Iron reacts with fluorine, chlorine, and bromine to give the corresponding ferric halides, ferric chloride being the most common. [13] 2 Fe + 3 X 2 → 2 FeX 3 (X = F, Cl, Br) Ferric iodide is an exception, being thermodynamically unstable due to the oxidizing power of Fe 3+ and the high reducing power of I −: [13] 2 I − + 2 Fe 3+ → I 2 ...

  3. Ferric chloride test - Wikipedia

    en.wikipedia.org/wiki/Ferric_chloride_test

    The sample is dissolved in water, or a mixture of water and ethanol, and a few drops of neutral ferric chloride (FeCl 3) solution, which is prepared by adding de-ionised water. Add sodium hydroxide to the mixture until a permanent brown precipitate is formed. The formation of a red, blue, green, or purple coloration indicates the presence of ...

  4. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C 6 H 5 OH. [5] It is a white crystalline solid that is volatile. The molecule consists of a phenyl group (−C 6 H 5) bonded to a hydroxy group (−OH). Mildly acidic, it requires careful handling because it can cause ...

  5. Iron(III) chloride - Wikipedia

    en.wikipedia.org/wiki/Iron(III)_chloride

    In addition to these simple stoichiometric reactions, the Lewis acidity of ferric chloride enables its use in a variety of acid-catalyzed reactions as described below in the section on organic chemistry. [10] In terms of its being an oxidant, iron(III) chloride oxidizes iron powder to form iron(II) chloride via a comproportionation reaction: [10]

  6. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    Phenol esters are active esters, being prone to hydrolysis. Phenols are reactive species toward oxidation. Oxidative cleavage, for instance cleavage of 1,2-dihydroxybenzene to the monomethylester of 2,4 hexadienedioic acid with oxygen, copper chloride in pyridine [4] Oxidative de-aromatization to quinones also known as the Teuber reaction.

  7. Carvacrol - Wikipedia

    en.wikipedia.org/wiki/Carvacrol

    It is extracted from Origanum oil by means of a 50% potash solution. It is a thick oil that sets at -20 °C to a mass of crystals of melting point 0 °C, and boiling point 236–237 °C. Oxidation with ferric chloride converts it into dicarvacrol, whilst phosphorus pentachloride transforms it into chlorcymol. [5]

  8. Oxidative coupling of phenols - Wikipedia

    en.wikipedia.org/wiki/Oxidative_coupling_of_phenols

    Oxidative coupling of phenols is a chemical reaction wherein two phenolic compounds are coupled via an oxidative process. Oxidative phenol couplings are often catalyzed by transition metal complexes including V , Cr , Mn , Cu , Fe , among others.

  9. Ferric - Wikipedia

    en.wikipedia.org/wiki/Ferric

    In chemistry, iron(III) or ferric refers to the element iron in its +3 oxidation state. Ferric chloride is an alternative name for iron(III) chloride (FeCl 3). The adjective ferrous is used instead for iron(II) salts, containing the cation Fe 2+. The word ferric is derived from the Latin word ferrum, meaning "iron".