When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/FriedelCrafts_reaction

    Friedel–Crafts alkylations can be reversible. Although this is usually undesirable it can be exploited; for instance by facilitating transalkylation reactions. [10] 1,3-Diisopropylbenzene is produced via transalkylation, a special form of Friedel–Crafts alkylation. It also allows alkyl chains to be added reversibly as protecting groups.

  3. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    A formylation reaction in organic chemistry refers to organic reactions in which an organic compound is functionalized with a formyl group (-CH=O). The reaction is a route to aldehydes (C-CH=O), formamides (N-CH=O), and formate esters (O-CH=O).

  4. Electrophilic aromatic substitution - Wikipedia

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

    This reaction is typically catalyzed by the corresponding iron or aluminum trihalide. The Friedel–Crafts reaction can be performed either as an acylation or as an alkylation. Often, aluminium trichloride is used, but almost any strong Lewis acid can be applied. For the acylation reaction a stoichiometric amount of aluminum trichloride is ...

  5. Fries rearrangement - Wikipedia

    en.wikipedia.org/wiki/Fries_rearrangement

    In addition to the ordinary thermal phenyl ester reaction a photochemical variant is possible. The photo-Fries rearrangement can likewise give [1,3] and [1,5] products, [7] [8] which involves a radical reaction mechanism. This reaction is also possible with deactivating substituents on the aromatic group. Because the yields are low this ...

  6. Stollé synthesis - Wikipedia

    en.wikipedia.org/wiki/Stollé_synthesis

    Download as PDF; Printable version; ... The Stollé synthesis is a series of chemical reactions that produce ... while the second step is a Friedel–Crafts reaction ...

  7. Electrophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_substitution

    In electrophilic substitution in aromatic compounds, an atom appended to the aromatic ring, usually hydrogen, is replaced by an electrophile.The most important reactions of this type that take place are aromatic nitration, aromatic halogenation, aromatic sulfonation and acylation and alkylating Friedel-Crafts reactions.

  8. Acylation - Wikipedia

    en.wikipedia.org/wiki/Acylation

    For example, Friedel–Crafts acylation uses acetyl chloride (CH 3 COCl) as the agent and aluminum chloride (AlCl 3) as a catalyst to add an acetyl group to benzene: [2] Friedel-Crafts acylation of benzene by ethanoyl chloride. This reaction is an example of electrophilic aromatic substitution.

  9. Friedel family - Wikipedia

    en.wikipedia.org/wiki/Friedel_family

    Friedel–Crafts reaction, a type of organic reaction developed by Charles Friedel and James Crafts in 1877. Friedel's law, named after Georges Friedel, the crystallographer, is a property of Fourier transforms of real functions.