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  2. Deprotonation - Wikipedia

    en.wikipedia.org/wiki/Deprotonation

    The hydrogen is dangerous and could ignite with the oxygen in the air, so the chemical procedure should be done in an inert atmosphere (e.g., nitrogen). Deprotonation can be an important step in a chemical reaction. Acid–base reactions typically occur faster than any other step which may determine the product of a reaction. The conjugate base ...

  3. Enol - Wikipedia

    en.wikipedia.org/wiki/Enol

    Deprotonation of organic carbonyls gives the enolate anion, which are a strong nucleophile. A classic example for favoring the keto form can be seen in the equilibrium between vinyl alcohol and acetaldehyde (K = [enol]/[keto] ≈ 3 × 10 −7). In 1,3-diketones, such as acetylacetone (2,4-pentanedione), the enol form is favored.

  4. Protonation - Wikipedia

    en.wikipedia.org/wiki/Protonation

    Protonation and deprotonation (removal of a proton) occur in most acid–base reactions; they are the core of most acid–base reaction theories. A Brønsted–Lowry acid is defined as a chemical substance that protonates another substance.

  5. Lithium diisopropylamide - Wikipedia

    en.wikipedia.org/wiki/Lithium_diisopropylamide

    The deprotonation of carbon acids can proceed with either kinetic or thermodynamic reaction control. Kinetic controlled deprotonation requires a base that is sterically hindered and strong enough to remove the proton irreversibly. For example, in the case of phenylacetone, deprotonation can produce two different enolates. LDA has been shown to ...

  6. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    deprotonation of the carbocation. E1 typically takes place with tertiary alkyl halides, but is possible with some secondary alkyl halides. The reaction rate is influenced only by the concentration of the alkyl halide because carbocation formation is the slowest step, as known as the rate-determining step .

  7. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane (/ ˈ h ɛ k s eɪ n /) or n-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C 6 H 14. [ 7 ] Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately 69 °C (156 °F).

  8. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    The lifetime of • HO radicals in the Earth atmosphere is very short, therefore • HO concentrations in the air are very low and very sensitive techniques are required for its direct detection. [9] Global average hydroxyl radical concentrations have been measured indirectly by analyzing methyl chloroform (CH 3 CCl 3 ) present in the air.

  9. Sodium bis(trimethylsilyl)amide - Wikipedia

    en.wikipedia.org/wiki/Sodium_bis(trimethylsilyl...

    This species, usually called NaHMDS (sodium hexamethyldisilazide), is a strong base used for deprotonation reactions or base-catalyzed reactions. Its advantages are that it is commercially available as a solid and it is soluble not only in ethers, such as THF or diethyl ether , but also in aromatic solvents, like benzene and toluene by virtue ...