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  2. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    5 c 6 h 5 ch 3 + 6 kmno 4 + 9 h 2 so 45 c 6 h 5 cooh + 14 h 2 o + 3 k 2 so 4 + 6 mnso 4 Glycols and polyols are highly reactive toward KMnO 4 . For example, addition of potassium permanganate to an aqueous solution of sugar and sodium hydroxide produces the chemical chameleon reaction, which involves dramatic color changes associated with ...

  3. Glycerol and potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Glycerol_and_potassium...

    The exothermic (heat producing) reaction between potassium permanganate (KMnO 4), a strong oxidizing agent, and glycerol (C 3 H 5 (OH) 3), a readily oxidised organic substance, is an example of an experiment sometimes referred to as a "chemical volcano". [7] [8]

  4. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    [4] Gattermann-Koch reaction: named after German chemists Ludwig Gattermann and Julius Arnold Koch, the Gattermann-Koch reaction is a catalyzed formylation of alkylbenzenes with carbon monoxide and hydrochloric acid. [5] Alkylbenzene sulfonation reaction: electrophilic addition of a sulfonic acid group onto the aromatic ring. [4]

  5. Benzonitrile - Wikipedia

    en.wikipedia.org/wiki/Benzonitrile

    Benzonitrile is a useful solvent and a versatile precursor to many derivatives. It reacts with amines to afford N-substituted benzamides after hydrolysis. [3] It is a precursor to diphenylmethanimine via reaction with phenylmagnesium bromide followed by methanolysis.

  6. Benzilic acid rearrangement - Wikipedia

    en.wikipedia.org/wiki/Benzilic_acid_rearrangement

    The benzilic acid rearrangement is formally the 1,2-rearrangement of 1,2-diketones to form α-hydroxy–carboxylic acids using a base. This reaction receives its name from the reaction of benzil with potassium hydroxide to form benzilic acid. First performed by Justus von Liebig in 1838, [1] it is the first reported example of a rearrangement ...

  7. Carbonyl oxidation with hypervalent iodine reagents - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_oxidation_with...

    A key iodine(III) enolate intermediate forms, which then undergoes either nucleophilic substitution (α-functionalization), elimination (dehydrogenation), or rearrangement. Common hypervalent iodine reagents used to effect these transformations include iodosylbenzene (PhIO), [1] Koser's reagent (PhI(OTs)OH), [1] and (dichloroiodo)benzene (PhICl ...

  8. tert-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylbenzene

    Its structure consists of a benzene ring substituted with a tert-butyl group. It is a flammable colorless liquid which is nearly insoluble in water but miscible with organic solvents. It is a flammable colorless liquid which is nearly insoluble in water but miscible with organic solvents.

  9. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Download QR code; Print/export ... The limit of the fusion process is the hydrogen-free allotrope of ... After exposure to 63 to 405 mg/m 3 of benzene for 1 to 5 ...