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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...

    Pages in category "Chlorobenzene derivatives" The following 164 pages are in this category, out of 164 total. This list may not reflect recent changes. 0–9.

  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:Chlorobenzenes - Wikipedia

    en.wikipedia.org/wiki/Category:Chlorobenzenes

    If the benzene ring contains other substituents, it belongs in Category:Chlorobenzene derivatives ... 1,2,4-Trichlorobenzene; 1,3,5-Trichlorobenzene

  6. 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

  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. 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:

  9. Category:Halobenzene compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Halobenzene_compounds

    Bromobenzene compounds (2 C) C. Chlorobenzene compounds (2 C, 5 P) F. Fluorobenzene compounds (2 C) H. Halobenzene derivatives (4 C, 1 P) Halobenzenes (5 C, 1 P) I.

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