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Arnold’s reagent

Dimethylamino)-4 -(diethylaniiiio)-diphenylmethane (Arnold s reagent) + 1,3-Dinitrobenzene... [Pg.69]

Arnold, S.M., Hickey. W.J.. and Harris. R.F. Degradation of atrazine by Fenton s reagent condition optimization and product quantification. Environ. Sci. Technol, 29(8) 2083-2089,1995. [Pg.1626]

Table 6.8 shows that the fastest depletion of atrazine occurs under Fenton s reagent. Arnold et al. (1995) demonstrated that OH may react with Ch at low pH to produce HOC1 and Cl2, causing underestimation of Cl concentrations, but the results suggest that Cl- scavenging by OH was minimal. Dechlorination and dealkylation occur simultaneously, and the batch treatment showed that dechlorination occurred more readily with alkylated s-triazines. Chlorinated products accounted for a large part of s-triazines present upon completion of Fenton s reagent. [Pg.227]

Degradation pathway for atrazine treated with Fenton s reagent. (From Arnold, S.M. et al., Environ. Sci. Technol., 29, 2083, 1995. With permission.)... [Pg.229]

Allylic esters having at least one aryl group and one H-atom attached to the a-carbon atom undergo intramolecular rearrangement, in the presence of strong basic reagents, to give a-allylic subst. acids.—E / -Methylallyl diphenylacetate boiled 22 hrs. in toluene with pulverized NaH—>- 2,2-diphenyl-4-methylpenten-4-oic acid. Y 76%. (F. e. s. R. T. Arnold andS. Searles, Jr., Am. Soc. 71,1150 (1949).)... [Pg.3]


See other pages where Arnold’s reagent is mentioned: [Pg.1553]    [Pg.226]    [Pg.228]    [Pg.228]    [Pg.316]    [Pg.663]    [Pg.663]    [Pg.345]    [Pg.455]    [Pg.269]   
See also in sourсe #XX -- [ Pg.123 ]

See also in sourсe #XX -- [ Pg.123 ]

See also in sourсe #XX -- [ Pg.123 ]




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