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  2. Bromophenol - Wikipedia

    en.wikipedia.org/wiki/Bromophenol

    They may be viewed as hydroxyl derivatives of bromobenzene, or as brominated derivatives of phenol. There are five basic types of bromophenols (mono- to pentabromophenol) and 19 different bromophenols in total when positional isomerism is taken into account. Bromophenols are produced by electrophilic halogenation of phenol with bromine.

  3. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    Bromobenzene is an aryl bromide and the simplest of the bromobenzenes, consisting of a benzene ring substituted with one bromine atom. Its chemical formula is C 6 H 5 Br . It is a colourless liquid although older samples can appear yellow.

  4. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    A few types of aromatic compounds, such as phenol, will react without a catalyst, but for typical benzene derivatives with less reactive substrates, a Lewis acid is required as a catalyst. Typical Lewis acid catalysts include AlCl 3, FeCl 3, FeBr 3 and ZnCl 2. These work by forming a highly electrophilic complex which is attacked by the benzene ...

  5. Electrophilic aromatic directing groups - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    Phenol is an ortho/para director, but in a presence of base, the reaction is more rapid. It is due to the higher reactivity of phenolate anion. The negative oxygen was 'forced' to give electron density to the carbons (because it has a negative charge, it has an extra +I effect).

  6. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    The Sandmeyer reaction is an example of a radical-nucleophilic aromatic substitution (S RN Ar). The radical mechanism of the Sandmeyer reaction is supported by the detection of biaryl byproducts. [8]

  7. Gattermann reaction - Wikipedia

    en.wikipedia.org/wiki/Gattermann_reaction

    Unlike the Gattermann reaction, this reaction is not applicable to phenol and phenol ether substrates. [5] Although the highly unstable formyl chloride was initially postulated as an intermediate, formyl cation (i.e., protonated carbon monoxide), [HCO] + , is now thought to react directly with the arene without the initial formation of formyl ...

  8. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    The direct reaction between phenol and paraformaldehyde is possible via the Casiraghi formylation, [4] but other methods apply masked forms of formaldehyde, in part to limit the formation of phenol formaldehyde resins. Aldehydes are strongly deactivating and as such phenols typically only react once.

  9. Monobromophenol - Wikipedia

    en.wikipedia.org/wiki/Monobromophenol

    The monobromophenols are chemical compounds consisting of phenol substituted with a bromine atom. There are three isomers , 2-bromophenol, 3-bromophenol, and 4-bromophenol. Bromophenols