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M-Chlorophenol

TRINITROBENZENE m-DIBROMOBENZENE m-CHLORONITROBENZENE o-CHLORONITROBENZENE p-CHLORONITROBENZENE tn-D I CHLOROBENZENE o-DICHLOROBENZENE p-DI CHLOROBENZENE m-DIFLUOROBENZENE o-DIFLUOROBENZENE p-DIFLUOROBENZENE m-DI NITROBENZENE o-DINITROBENZENE p-DINITROBENZENE BROMOBENZENE MONOCHLOROBENZENE m-CHLOROPHENOL o-CHLOROPHENOL p-CHLOROPHENOL... [Pg.184]

Problem 19,14 Assign numbers from 1 for least to 4 for most to indicate the relative acid strengths in the following groups (a) phenol, m-chlorophenol, m-nitrophenol, m-cresol (b) phenol, benzoic acid, p-nitro-phenol, carbonic acid (c) phenol, p-chlorophenol, p-nitrophenol, p-cresol (d) phenol, o-nitrophenol, m-nitrophenol, p-nitrophenol (e) phenol, p-chlorophenol, 2,4,6-trichlorophenol, 2,4-dichlorophenol (/) phenol, benzyl alcohol, benzenesulfonic acid, benzoic acid. ... [Pg.444]

Compound from m-Chlorophenol.—Repeated washing of the compound (C6H5)5Cr.O.C6H4Cl.HO.C6H4.Cl (p. 264) with ether yields a tetraphenyl derivative, (C6H5)4Cr.O.C6H4.Cl.HO.C6H4.Cl, M.pt. 130° C. [Pg.268]

The inwitro metabolites of chlorobenzene are o-chlorophenol, m- chlorophenol, and p-chlorophenol the proportions differ according to the source of the mono-oxygenase system and its state of purity (Selander et al. 1975). The o- and p-chlorophenols result from isomerization of the intermediate 3-and 4-chlorobenzene oxides, respectively. The formation of m-chlorophenol appears to occur via a direct oxidative pathway (Oesch et al. 1973). In vitro conjugation of the arene oxide with glutathione or hydration is not a significant pathway (Selander et al. 1975). [Pg.37]

Lindsay-Smith et al. (1972) reported that the major metabolites of chlorobenzene in the rabbit are p-chlorophenylmercapturic acid and conjugates of 4-chlorocatechol. Other urinary metabolites included quinol, 3- chlorocatechol, and o-and m-chlorophenylmercapturic acids. Oesch et al. (1973) studied the metabolism of chlorobenzene in rats administered chlorobenzene by intraperitoneal injection. Thirty-three percent of the administered dose was excreted in the urine, with p-chlorophenol as the major metabolite. Other metabolites included 4-chlorocatechol, o-chlorophenol, and m- chlorophenol. [Pg.37]

Davis and his co-workers [127,128] found chlorobenzene also undergoes oxynitration by action of 65% nitric acid, with formation of trinitro-m-chlorophenol along with chlo-ronitrobenzenes, while naphthalene when nitrated with more dilute acid, for example, at a concentration of 65%, yielded 2,4-dinitro-a-naphthol besides 2-nitro-a-naphthol. [Pg.111]

Chloro 6 nitro toluene bifenox, fomesafen, lactofen, perfluidone m-Chloro perbenzoic acid fipronil, rimsulfuron m-Chlorophenol cloprop, 3 CPA, oxyfluorfen... [Pg.1030]

Sample Problem 25.6 Synthesize m-chlorophenol from benzene. [Pg.985]

See other pages where M-Chlorophenol is mentioned: [Pg.685]    [Pg.998]    [Pg.1195]    [Pg.285]    [Pg.451]    [Pg.468]    [Pg.979]    [Pg.998]    [Pg.1195]    [Pg.685]    [Pg.29]    [Pg.737]    [Pg.38]    [Pg.65]    [Pg.93]    [Pg.158]    [Pg.177]    [Pg.124]    [Pg.685]    [Pg.493]    [Pg.63]    [Pg.184]    [Pg.1005]    [Pg.1202]    [Pg.261]    [Pg.264]    [Pg.29]    [Pg.1312]    [Pg.1040]    [Pg.563]    [Pg.44]    [Pg.472]    [Pg.93]    [Pg.1312]    [Pg.122]    [Pg.341]    [Pg.1579]    [Pg.630]    [Pg.633]   
See also in sourсe #XX -- [ Pg.126 ]

See also in sourсe #XX -- [ Pg.54 ]

See also in sourсe #XX -- [ Pg.54 ]

See also in sourсe #XX -- [ Pg.822 ]

See also in sourсe #XX -- [ Pg.120 ]

See also in sourсe #XX -- [ Pg.892 ]



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