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  2. 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 ...

  3. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    Total phenols (or antioxidant effect) can be measured using the Folin-Ciocalteu reaction. Results are typically expressed as gallic acid equivalents (GAE). Ferric chloride (FeCl 3) test is also a colorimetric assay. Lamaison and Carnet have designed a test for the determination of the total flavonoid content of a sample (AlCI 3 method). After ...

  4. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    When a mixture of phenol and benzoyl chloride are shaken in presence of dilute sodium hydroxide solution, phenyl benzoate is formed. This is an example of the Schotten–Baumann reaction : C 6 H 5 COCl + HOC 6 H 5 → C 6 H 5 CO 2 C 6 H 5 + HCl

  5. 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 ...

  6. Iron(III) chloride - Wikipedia

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

    Aqueous iron(III) chloride serves as a one-electron oxidant illustrated by its reaction with copper(I) chloride to give copper(II) chloride and iron(II) chloride. FeCl 3 + CuCl → FeCl 2 + CuCl 2. This fundamental reaction is relevant to the use of ferric chloride solutions in etching copper.

  7. 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.

  8. Tannin - Wikipedia

    en.wikipedia.org/wiki/Tannin

    Tannins produce different colors with ferric chloride (either blue, blue black, or green to greenish-black) according to the type of tannin. Iron gall ink is produced by treating a solution of tannins with iron(II) sulfate. [72] Tannins can also be used as a mordant, and is especially useful in natural dyeing of cellulose fibers such as cotton ...

  9. Prussian blue - Wikipedia

    en.wikipedia.org/wiki/Ferric_ferrocyanide

    Samples and phenolic standards are given acidic ferric chloride and ferricyanide, which is reduced to ferrocyanide by the phenols. The ferric chloride and ferrocyanide react to form Prussian blue. Comparing the absorbance at 700 nm of the samples to the standards allows for the determination of total phenols or polyphenols. [53] [54]