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  2. Permanganate - Wikipedia

    en.wikipedia.org/wiki/Permanganate

    A permanganate (/ p ər ˈ m æ ŋ ɡ ə n eɪ t, p ɜːr-/) [1] is a chemical compound with the manganate(VII) ion, MnO − 4 , the conjugate base of permanganic acid . Because the manganese atom has a +7 oxidation state , the permanganate(VII) ion is a strong oxidising agent .

  3. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    The value determined is known as the permanganate value. In analytical chemistry, a standardized aqueous solution of KMnO 4 is sometimes used as an oxidizing titrant for redox titrations (permanganometry). As potassium permanganate is titrated, the solution becomes a light shade of purple, which darkens as excess of the titrant is added to the ...

  4. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Toluene (/ ˈ t ɒ l. j u iː n /), also known as toluol (/ ˈ t ɒ l. j u. ɒ l , - ɔː l , - oʊ l / ), is a substituted aromatic hydrocarbon [ 15 ] with the chemical formula C 6 H 5 CH 3 , often abbreviated as PhCH 3 , where Ph stands for the phenyl group.

  5. Magnesium permanganate - Wikipedia

    en.wikipedia.org/wiki/Magnesium_permanganate

    Magnesium permanganate is used in various branches of industry and technology, such as: [2] a wood impregnation agent. an additive in tobacco filters. as a catalyst in the air oxidation of toluene to benzoic acid and in proteome research.

  6. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    Reagents useful for the transformation of primary alcohols to aldehydes are normally also suitable for the oxidation of secondary alcohols to ketones. These include Collins reagent and Dess-Martin periodinane. The direct oxidation of primary alcohols to carboxylic acids can be carried out using potassium permanganate or the Jones reagent.

  7. 18-Crown-6 - Wikipedia

    en.wikipedia.org/wiki/18-Crown-6

    For example, potassium permanganate dissolves in benzene in the presence of 18-crown-6, giving the so-called "purple benzene", which can be used to oxidize diverse organic compounds. [1] Various substitution reactions are also accelerated in the presence of 18-crown-6, which suppresses ion-pairing. [10] The anions thereby become naked nucleophiles.

  8. Chlorotoluene - Wikipedia

    en.wikipedia.org/wiki/Chlorotoluene

    Chlorotoluenes are aryl chlorides based on toluene in which at least one aromatic hydrogen atom is replaced with a chlorine atom. They have the general formula C 7 H 8–n Cl n, where n = 1–5 is the number of chlorine atoms.

  9. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    Alkenes can be oxidized with ozone to form alcohols, aldehydes or ketones, or carboxylic acids.In a typical procedure, ozone is bubbled through a solution of the alkene in methanol at −78 °C (−108 °F; 195 K) until the solution takes on a characteristic blue color, which is due to unreacted ozone.