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  2. n-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/N-Butylbenzene

    Of two isomers of butylbenzene, n-butylbenzene consists of a phenyl group attached to the 1 position of a butyl group. It is a slightly greasy, colorless liquid. The synthesis of n-butylbenzene by the reaction of chlorobenzene and butylmagnesium bromide was one of the first demonstrations of the Kumada coupling using nickel diphosphine ...

  3. Glycerol and potassium permanganate - Wikipedia

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

    Crystalline potassium permanganate (KMnO 4) is placed in an evaporating dish. A depression is made at the center of the permanganate powder and glycerol liquid is added to it. The white smoke-like vapor produced by the reaction is a mixture of carbon dioxide gas and water vapor.

  4. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    In chemistry, a reaction mechanism is the step by step sequence of elementary reactions by which overall chemical reaction occurs. [ 1 ] A chemical mechanism is a theoretical conjecture that tries to describe in detail what takes place at each stage of an overall chemical reaction.

  5. Potassium manganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_manganate

    Potassium permanganate will decompose into potassium manganate, manganese dioxide and oxygen gas: 2 KMnO 4 → K 2 MnO 4 + MnO 2 + O 2. This reaction is a laboratory method to prepare oxygen, but produces samples of potassium manganate contaminated with MnO 2. The former is soluble and the latter is not.

  6. Michaelis–Menten kinetics - Wikipedia

    en.wikipedia.org/wiki/Michaelis–Menten_kinetics

    Biochemical reactions involving a single substrate are often assumed to follow Michaelis–Menten kinetics, without regard to the model's underlying assumptions. Only a small proportion of enzyme-catalysed reactions have just one substrate, but the equation still often applies if only one substrate concentration is varied.

  7. N-tert-Butylbenzenesulfinimidoyl chloride - Wikipedia

    en.wikipedia.org/wiki/N-Tert-butylbenzenesulfini...

    N-tert-Butylbenzenesulfinimidoyl chloride is a useful oxidant for organic synthesis reactions. [1] It is a good electrophile, and the sulfimide S=N bond can be attacked by nucleophiles, such as alkoxides, enolates, and amide ions. The nitrogen atom in the resulting intermediate is basic, and can abstract an α-hydrogen to create a new double bond.

  8. 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.

  9. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    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]

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