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Ring-Substituted Aromatics

T0025 Akzo Nobel MPP Systems, Macro Porous Polymer (MPP) [Pg.220]

T0029 Alternative Technologies for Waste, Inc., Detoxifier In Situ Steam/Hot-Air Stripping Unit [Pg.220]

T0135 Calgon Carbon Corporation, Activated Carbon T0136 Calgon Carbon Oxidation Technologies, Rayox [Pg.220]

T0138 Calgon Carbon Corporation, Perox-Pure [Pg.220]

T0199 Dehydro-Tech Corporation, Carver-Greenfield Process [Pg.220]


DDD Dichloro(chlorophenyl)-bis Ethane DDE Dichlorodiphenyldichloroethylene Dichlorobenzene, 1,2 Dichlorobenzene, 1,3 Dichlorobenzene, 1,4 Hexachlorobenzene Polychlorinated Benzenes Polychlorinated Biphenyls PCBs Aroclor Ring-Substituted Aromatics Tetrachlorobenzene Trichlorobenzene, 1,2,4 Saturated Alkyl Halides Bromodichloromethane Bromoform Tribromomethane Butyl Chloride Chlorobutane Carbon Tetrachloride Carbon Tetrafluoride Chloroform Trichloromethane Chloromethane Methyl Chloride Dibromochloromethane Dibromoethane, 1,2 Ethylene Dibromide Dibromomethane... [Pg.8]

Chlorobenzene Monochlorobenzene under Ring-Substituted Aromatics Chloroform Tiichloromethane under Saturated Alkyl HaUdes Chloromethane Methyl Chloride under Saturated Alkyl Halides Chlorophenol under Halophenols Chlorotoluene, 2 under Ring-Substituted Aromatics... [Pg.1266]

DDD Dichloro(chlorophenyl)-bis Ethane under Ring-Substituted Aromatics DDE Dichlorodiphenyldichloroethylene under Ring-Substituted Aromatics DDT Trichloro(chlorophenyl-l,4- bis) Ethane under Aromatics with Halogenated Side Chain Decane, n under Alkanes and Cyclic Alkanes... [Pg.1266]

Heterocyclic Sulfur Compounds with Two or More Rings Hexachlorobenzene under Ring-Substituted Aromatics Hexachlorobutadiene under Unsaturated Alkyl Halides Hexachlorocyclohexane Lindane under Saturated Alkyl Halides Hexachlorocyclopentadiene under Unsaturated Alkyl Halides Hexachloroethane under Saturated Alkyl Halides Hexadecane under Alkanes and Cyclic Alkanes Hexafluoroethane under Saturated Alkyl Halides Hexamethyldisihzane under Silicon Compounds—Other Significant Hexanes under Alkanes and Cyclic Alkanes Hexylamine under Primary Aliphatic Amines and Diamines... [Pg.1267]

Polychlorinated Benzenes under Ring-Substituted Aromatics Polychlorinated Biphenyls PCBs Aroclor under Ring-Substituted Aromatics... [Pg.1269]

RDX, Cyclonite, Hexahydro-l,3,5-trinitro-l,3,5-triazine under Secondary Aliphatic Amines Ring-Substituted Aromatics Saturated Alkyl Halides Secondary Alcohols... [Pg.1269]

Tetracblorobenzene under Ring-Substituted Aromatics Tetracbloroethane, 1,1,2,2 under Saturated Alkyl Halides Tetracbloroethene Percbloroethylene PCE under Unsaturated Alkyl Halides Tetracblorophenol under Halophenols... [Pg.1270]

The best substrates for ophidian L-amino acid oxidases are aromatic or, most generally, hydrophobic amino acids, polar and basic amino acids being deami-nated at much lower rates Glu, Asp, and Pro are not oxidized by L-amino add oxidase. L-Amino add oxidase is also active on ring-substituted aromatic amino acids, as well as on seleno cysteinyl derivatives. The substrate specificity depends on the source of the enzyme (e.g. Ophiophagus hannah L-amino acid oxidase also oxidizes Lys and Om) and on the pH. The of the reaction of Crotalus adaman-... [Pg.216]

Aromatic ring, substituted aromatic Heterocyclic ring Cycloaliphatic group... [Pg.206]

Esters of ring-substituted aromatic acids, e.g., R-O-CO-aryl Esters of derivatized phosphoric acids, e.g., R-0-P0(0R )(0R")... [Pg.486]

Synthesis and Properties of Sequentially Ordered Copolyesters and Re-gioregularly Ring Substituted Aromatic Homopolyesters... [Pg.4]

In addition, synthetic approaches and general properties of regioregularly ring substituted aromatic polyesters are described in this report ... [Pg.286]

Aryl diazonium ions undergo a variety of reactions that make them versatile intermediates for preparing a host of ring-substituted aromatic con xiunds. In these reactions, summarized... [Pg.887]

Ring-substituted aromatic halogen derivatives are much less reactive than acyclic halogen derivatives. Side-chain substituted aromatic compounds such as toluene derivatives, are as reactive as acyclic derivatives. [Pg.458]


See other pages where Ring-Substituted Aromatics is mentioned: [Pg.1140]    [Pg.946]    [Pg.946]    [Pg.701]    [Pg.1140]    [Pg.8]    [Pg.220]    [Pg.221]    [Pg.223]    [Pg.225]    [Pg.227]    [Pg.229]    [Pg.230]    [Pg.231]    [Pg.233]    [Pg.235]    [Pg.1266]    [Pg.1266]    [Pg.1266]    [Pg.1270]    [Pg.527]    [Pg.1140]    [Pg.953]    [Pg.693]    [Pg.566]    [Pg.1140]    [Pg.152]    [Pg.891]    [Pg.1140]    [Pg.891]    [Pg.961]    [Pg.32]    [Pg.197]    [Pg.373]   


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Aromatic Compounds—Substituted Benzene Rings

Aromatic ring substitution

Aromatic ring substitution

Aromatic rings substitution patterns, infrared

Aromatic rings, oxidation ipso substitution

Aromatic substitution ring closure with

Aromatic, acidity ring substitution

Attack on Substituted Aromatic Rings

Degree of aromatic ring substitution

Fused rings, electrophilic aromatic substitution

Fused-ring compounds aromatic substitution

Rigidity, aromatic ring substitution

Ring substitution

Ring substitution in aromatic amines

Substituent Effects in Substituted Aromatic Rings

Substitution Reactions of Polymers with Aromatic Rings

Substitution at Aromatic Rings

Substitution, electrophilic fused ring aromatics

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