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  2. Phenacyl chloride - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_chloride

    Phenacyl chloride, also commonly known as chloroacetophenone, is a substituted acetophenone. It is a useful building block in organic chemistry . Apart from that, it has been historically used as a riot control agent , where it is designated CN . [ 5 ]

  3. Category:Chlorobenzene derivatives - Wikipedia

    en.wikipedia.org/wiki/Category:Chlorobenzene...

    This page was last edited on 31 January 2024, at 19:46 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  4. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.

  5. Category:Chlorobenzene compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Chlorobenzene...

    Pages in category "Chlorobenzene compounds" The following 5 pages are in this category, out of 5 total. ... This page was last edited on 1 February 2024, ...

  6. Category:Chlorobenzenes - Wikipedia

    en.wikipedia.org/wiki/Category:Chlorobenzenes

    If the benzene ring contains other substituents, it belongs in Category:Chlorobenzene derivatives The main article for this category is Chlorobenzenes . Pages in category "Chlorobenzenes"

  7. Dow process (phenol) - Wikipedia

    en.wikipedia.org/wiki/Dow_process_(phenol)

    When 1-[14 C]-1-chlorobenzene was subjected to aqueous NaOH at 395 °C, ipso substitution product 1-[14 C]-phenol was formed in 54% yield, while cine substitution product 2-[14 C]-phenol was formed in 43% yield, indicating that an elimination-addition (benzyne) mechanism is predominant, with perhaps a small amount of product from addition ...

  8. 4,4'-Dichlorobenzophenone - Wikipedia

    en.wikipedia.org/wiki/4,4'-dichlorobenzophenone

    4,4’-Dichlorobenzophenone is prepared by the acylation of chlorobenzene with 4-chlorobenzoyl chloride. The conversion is typically conducted in the presence of an aluminium chloride catalyst in a petroleum ether solvent. ClC 6 H 5 C(O)Cl + C 6 H 5 Cl → (ClC 6 H 4) 2 CO + HCl

  9. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    The most commonly employed Sandmeyer reactions are the chlorination, bromination, cyanation, and hydroxylation reactions using CuCl, CuBr, CuCN, and Cu 2 O, respectively. More recently, trifluoromethylation of diazonium salts has been developed and is referred to as a 'Sandmeyer-type' reaction.