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O-Chlorobiphenyl

King TL, Haines BK, Uthe JF. 1996. Non-, mono-, and di-o-chlorobiphenyl concentrations and their toxic equivalents to 2,3,7,8-tetrachlorodibenzo(p)dioxin in Aroclors and digestive glands from American lobster (homarus americanus) captured in Atlantic Canada. Bull Environ Contam Toxicol 57 465-472. [Pg.769]

It has beeia found by Britton that when an aryl or alkyl-substituted aromatic halohydrocarbon is hydrolyzed at a relatively high temperature, i.e., 30(MOO C, in the absence of copper, there is formed a substituted phenol in which the hydroxyl group is in a position that is ortho or para to the (Higinal position of the halogen, together with a certain amount of the expected phenol. For example, both o-phenylphenol and p-phenyl-phenol are prepared from o-chlorobiphenyl. [Pg.759]

See other pages where O-Chlorobiphenyl is mentioned: [Pg.517]    [Pg.517]    [Pg.1311]    [Pg.524]    [Pg.292]    [Pg.310]    [Pg.671]    [Pg.578]    [Pg.225]    [Pg.247]    [Pg.247]    [Pg.225]    [Pg.247]    [Pg.485]    [Pg.485]    [Pg.1541]    [Pg.1559]    [Pg.1920]    [Pg.292]    [Pg.310]    [Pg.671]    [Pg.503]    [Pg.167]    [Pg.753]   


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Chlorobiphenyls

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