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  2. Hydroxyacetophenone - Wikipedia

    en.wikipedia.org/wiki/Hydroxyacetophenone

    3-Hydroxyacetophenone (m-hydroxyacetophenone) 4-Hydroxyacetophenone (p-hydroxyacetophenone, piceol) This page was last edited on 27 February ...

  3. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    Chemical structure of piceol. Names Preferred IUPAC name. 1-(4-Hydroxyphenyl)ethan-1-one ... 4-Hydroxyacetophenone monooxygenase is an enzyme that transforms piceol ...

  4. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:

  5. Fries rearrangement - Wikipedia

    en.wikipedia.org/wiki/Fries_rearrangement

    A low reaction temperature favors para substitution and with high temperatures the ortho product prevails, this can be rationalised as exhibiting classic thermodynamic versus kinetic reaction control as the ortho product can form a more stable bidentate complex with the aluminium. [5]

  6. 3-Hydroxyacetophenone - Wikipedia

    en.wikipedia.org/wiki/3-hydroxyacetophenone

    3-Hydroxyacetophenone is a chemical compound. It is a component of castoreum, the exudate from the castor sacs of the mature beaver. [1] Related compounds.

  7. Salicylaldehyde - Wikipedia

    en.wikipedia.org/wiki/Salicylaldehyde

    Salicylaldehyde is produced by condensation of phenol with formaldehyde to give hydroxybenzyl alcohol, which is oxidized to the aldehyde. [4] Salicylaldehydes in general are prepared by ortho-selective formylation reactions from the corresponding phenol, for instance by the Duff reaction, Reimer–Tiemann reaction, or by treatment with paraformaldehyde in the presence of magnesium chloride and ...

  8. Ortho acid - Wikipedia

    en.wikipedia.org/wiki/Ortho_acid

    In organic chemistry, ortho acids are organic, hypothetical chemical compounds having the structure R−C(OH) 3 (R = alkyl or aryl). [1] Ortho acids themselves are unstable and cannot be isolated. However, ortho esters can be synthesized by the Pinner reaction, in which nitriles react with alcohols under acid catalysis: RCN + 3 R'OH → RC(OR ...

  9. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    Ortho effect is an organic chemistry phenomenon where the presence of a chemical group at the at ortho position or the 1 and 2 position of a phenyl ring, ...