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Halogenated aromatic compounds restrictions

The plausibility that PCB effects on reproductive function (and other functions such as neurobehavior and immunological competence) may involve PCB effects on endocrine functions has led to investigations of the estrogenic and anti-estrogenic activities of PCB mixtures and individual congeners, and the effects of PCBs or related halogenated aromatic compounds on steroid hormone metabolism via induction of Phase I or Phase n enzymes. How these PCB effects are specifically related to PCB effects on reproductive function is unknown, but the results of these investigations provide further evidence that reproductive effects from PCB mixtures may not be restricted to Ah-receptor mediation alone and are likely to involve multiple mechanisms that have yet to be elucidated. Related information on endocrine disruption is discussed in Section 3.6. [Pg.403]

Electrophilic aromatic substitution is the most important reaction of aromatic compounds because it has broad applications for a wide variety of aromatic compounds. In contrast, nucleophilic aromatic substitution has restricted applications. In nucleophilic aromatic substitution, a strong nucleophile replaces a leaving group, such as a halide. What is the mechanism of nucleophilic aromatic substitution It cannot be the S]m2 mechanism because aryl halides cannot achieve the correct geometry fw back-side displacement The aromatic ring blocks approach of the nucleophile to the back of the carbon bearing the halogen. [Pg.780]

Successful thermal decarboxylation of metal arenoates other than poly-halogenoarenoates are restricted to mercury compounds and fall into three categories, namely (i) those where electron-withdrawing substituents other than halogens are present in the organic groups, (ii) those where substituents and/or conditions are used which favor a different mechanism, e.g., classic electrophilic aromatic substitution, or (iii) those where the conditions are sufficiently forcing for both mercuration and decarboxylation to occur. [Pg.255]

This technology has been used to treat polychlorinated biphenyls (PCBs), halogenated and nonhalogenated solvents, semivolatile organic compounds (SVOCs), polynuclear aromatic hydrocarbons (PAHs), pesticides, herbicides, fuel oils, benzene, toluene, ethylbenzene, and xylenes (BTEX), and mercury. This system has also treated Resource Conservation and Recovery Act (RCRA) hazardous wastes such as petroleum refinery wastes and multisource leachate treatment residues to meet RCRA Land Disposal Restrictions (LDR) treatment standards. [Pg.1118]


See other pages where Halogenated aromatic compounds restrictions is mentioned: [Pg.332]    [Pg.20]    [Pg.322]    [Pg.11]    [Pg.319]    [Pg.211]    [Pg.833]    [Pg.165]    [Pg.13]    [Pg.92]    [Pg.324]    [Pg.36]    [Pg.6]    [Pg.336]    [Pg.192]    [Pg.152]    [Pg.430]   
See also in sourсe #XX -- [ Pg.111 ]




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Aromatic compounds halogenation

Aromatics halogenation

Aromatics halogens

Aromatics, halogenated

Halogen compounds

Halogen compounds aromatic

Halogenated aromatic

Halogenation compounds

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