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In halogenation

In order to probe the importance of van der Waals interactions between reactants and solvent, experiments in the gas-liqnid transition range appear to be mandatory. Time-resolved studies of the density dependence of the cage and clnster dynamics in halogen photodissociation are needed to extend earlier quantum yield studies which clearly demonstrated the importance of van der Waals clnstering at moderate gas densities [37, 111]... [Pg.861]

NakatsujI H, Kuwano R, Merita H and Nakal H 1993 Dipped adcluster model and SAC-CI method applied to harpooning, chemical luminescence and electron emission in halogen chemisorption on alkali metal surface J. Mol. Catal. 82 211-28... [Pg.2235]

Numerous ionic compounds with halogens are known but a noble gas configuration can also be achieved by the formation of a covalent bond, for example in halogen molecules, X2, and hydrogen halides, HX. When the fluorine atom acquires one additional electron the second quantum level is completed, and further gain of electrons is not energetically possible under normal circumstances, i.e... [Pg.312]

Aniline.—Burns with a very smoky flame, clouds of soot being produced. Typical of many aromatic substances. i,2 Dibromoethane.—Does not burn until vapour becomes hot and then burns with a slightly smoky flame. Typical of substances rich in halogens such as cldoroform, chloral hydrate, and carbon, tetrachloride. (Note, however, that iodoform evolves copious fumes of iodine when heated in this way.)... [Pg.319]

Use of an excess of the halogenating agent results in halogenation at the 3-position of the oxindole[3,4]. The halogenation and hydrolysis can be carried out as two separate steps. One optimized procedure of this type used NCS as the halogenating agent and it was found that 70% phosphoric acid in 2-mcthoxycthanol was the most effective medium for hydrolysis[2]. If the halogenation is carried out in pyridine, the intermediate is trapped as an... [Pg.152]

Volatile impurities, eg, F2, HF, CIF, and CI2, in halogen fluoride compounds are most easily deterrnined by gas chromatography (109—111). The use of Ftoroplast adsorbents to determine certain volatile impurities to a detection limit of 0.01% has been described (112—114). Free halogen and haHde concentrations can be deterrnined by wet chemical analysis of hydrolyzed halogen fluoride compounds. [Pg.187]

Another use of hydrogen fluoride, although not in halogen exchange, is the reaction with ethylenes or acetylenes to form the addition products, 1,1-difluoroethane [75-37-6] and vinyl fluoride [75-02-5]-. [Pg.268]

E. Hengge in V. Gutmaim, ed.. Inorganic Silicon Halides in Halogen Chemistry, Vol. 2, Academic Press, Inc., New York, 1967. [Pg.20]

J. A. Goldstein and S. Safe, in Halogenated Biphenyls, Naphthalenes, Bihenzodioxins and Related Compounds, ed. R. D. Kimborough and A. A. Jensen, Elsevier, Amsterdam, 1989, p. 239. [Pg.13]

Allenes react with other typical electrophiles such as the halogens and mercuric ion. In systems where bridged-ion intermediates would be expected, nucleophilic capture generally occurs at the allylic position. This pattern is revealed, for example, in the products of solvent capture in halogen additions and by the structures of mercuration products. ... [Pg.377]

Perfluorinated organic bromides can be oxidatively fluonnated with elemental fluorine to derivatives containing tn- [124] and pentavalent [/25 126 127] bromine in yields up to 42% Perfluoroheptylbromine tetrafluoride has been used to fluonnate double bonds in halogenated alkenes [127]... [Pg.48]

Ford, C L In Halogenated Fire Suppressants, Gann, R G, Ed, ACS Symposium Senes 16, Amencan Chemical Society Washington, DC, 1975, pp 1-63... [Pg.1100]

The presence of an TV-oxide group activates the 1,2,4-triazine ring toward electrophilic attack, for instance, in halogenation reactions. Thus, 3-methoxy- and 3-amino(alkylamino)-1,2,4-triazine 1-oxides 16 react easily with chlorine or bromine to form the corresponding 6-halo-1,2,4-triazine 1-oxides 17 (77JOC3498, 78JOC2514). [Pg.268]

Table 6.5 Corrosion ratings of noble metals in halogens ... Table 6.5 Corrosion ratings of noble metals in halogens ...
Interactive to use a web-based palette to predict products in halogenation and alkylation reactions of carbonyl enolates. [Pg.855]

It is not unusual in halogen chemistry to find striking differences in the chemistry of acidic and... [Pg.360]


See other pages where In halogenation is mentioned: [Pg.194]    [Pg.404]    [Pg.476]    [Pg.260]    [Pg.329]    [Pg.390]    [Pg.443]    [Pg.56]    [Pg.174]    [Pg.643]    [Pg.927]    [Pg.452]    [Pg.225]    [Pg.272]    [Pg.368]    [Pg.504]    [Pg.588]    [Pg.806]    [Pg.1236]    [Pg.287]    [Pg.197]    [Pg.216]    [Pg.926]   
See also in sourсe #XX -- [ Pg.323 ]

See also in sourсe #XX -- [ Pg.77 ]




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Aromatic Halogen Compounds Substituted in the Side hain

Atomic Versus Molecular Elimination in Halogenated Hydrocarbons

Calculation of Energy Barriers for Elementary Steps in Hydrogen-Halogens Reactions

Carbanions in halogenation of ketones

Catalyst in additions of halogen

Determination of nitroaromatics and higher-boiling halogenated compounds in water

Drivers for Performing Halogenation of Acids in Micro Reactors

Elimination, and Halogenation Reactions in Polymers

Enamines as intermediates in isotope exchange and halogenation reactions

Enols in halogenation of ketones

Equilibria in Halogen Redistribution

Fillers for Use in Conjunction with Halogens

Flame retardants iron compounds, their effect on fire and smoke in halogenated polymers

Free halogens in halogenated solvents

Gallium in Halogen Acid Media

Halogen Chemistry in the Troposphere

Halogen Emission in Flow Discharge Systems

Halogen Photodissociation in Rare Gas Solids

Halogen-containing antibiotics in aquatic organisms

Halogen-containing antibiotics in terrestrial organisms

Halogenated Compounds, Photochemical Processes in (Majer and Simons)

Halogenated Compounds, Photochemical Processes in (Major and Simons)

Halogenated Polyhydrocarbons with Aromatic Rings in the Backbone

Halogenation as a Tool in Organic Synthesis

Halogenation in acid

Halogenation in base

Halogenation in general

Halogenation in water

Halogenation reactions in polymers

Halogens in Organic Synthesis Some Classical Reactions

Halogens in acids

Halogens in alkyl halides

Halogens in aromatic SrnI reactions

Halogens in organic combination

Halogens in organic synthesis

Halogens in positive oxidation states

Hypobromites in additions halogen fluondes

In additions halogen fluondes

In additions of halogen

In additions of halogen fluondes

In additions of halogen fluonne

In additions of halogen fluorides

In halogen-containing polymers

In halogen-free polymers

In the halogenation

Intermediates in addition halogen fluondes to double

Iron salts as catalysts in halogenation

Iron salts as catalysts in halogenation arenes

Oxidizing strength of the halogens in aqueous solution

POLARONS AND SOLITONS IN HALOGEN-BRIDGED PLATINUM COMPLEXES

Possible Role of Idiosyncrasy in Hepatitis Associated with Halogenated Volatile Anaesthetics

Reactivity in halogenation

Relaxation in Molecules or Ions With Covalently Bonded Halogens

Replacement of OH by halogen in phenols or heterocycles

Replacement of hydrogen by halogen in acetylenes

Replacement of hydrogen by halogen in aldehydes and ketones

Replacement of hydrogen by halogen in aliphatic dicarboxylic acids and nitriles

Replacement of hydrogen by halogen in aliphatic monocarboxylic acids

Replacement of hydrogen by halogen in alkanes

Replacement of hydrogen by halogen in aromatic compounds general

Replacement of hydrogen by halogen in aromatic nitro compounds

Replacement of hydrogen by halogen in ethers

Replacement of hydrogen by halogen in heterocycles

Replacement of hydrogen by halogen in olefins

Replacement of hydrogen by halogen in phenols, hydroxyphenylalkanoic acids, aryl ethers, and aromatic amines

Selectivity in Halogenation

Selectivity in Radical Halogenation with Fluorine and Bromine

Shielding Effects in Covalent Halogen Compounds

Substituent Effects in Electrophilic Aromatic Substitution Halogens

Systematic determination of highly volatile halogenated hydrocarbons (HHC) in water samples using gas chromatography

The displacement of halogen by cyanide in an aryl halide

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