Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Bromide compounds

The 2-thienylzinc bromide compound was prepared according to the same process described above in a 45% yield (equation 32)39. However, a different procedure has been used for the preparation of the 3-thienylzinc bromide compound41. [Pg.772]

On heating in carbon tetrachloride with tetrabutylammonium bromide, compounds 74 and 75, that is, the products of photobromination of tetra-O-... [Pg.83]

Compound B is an alkene derived from compound A—an alkyl bromide of molecular formula C7H15Br. We are told that compound A is not a primary alkyl bromide. Compound A can therefore be only ... [Pg.148]

Alkene C can only therefore be 2,3,3,4-tetramethyl-l-pentene. The two alkyl bromides, compounds A and B, that give this alkene on dehydrobromination have their bromine substituents at C-l and C-2, respectively. [Pg.148]

What results from a treatment of perfluorocyclobutene with anhydrous aluminum chloride (compound S) or aluminum bromide (compound T) ... [Pg.11]

When ethyl chlorofluoroacetate is treated with phenylmagnesium bromide, compound U is formed. This compound reacts with methylmagne-sium bromide to give compound V. Refluxing of the product in tetra-hydrofuran affords compound W. What are compounds U, V, and W, and how are they formed ... [Pg.28]

Contaminants may arise from impure starting materials, incomplete reactions and secondary reaction products. A knowledge of these factors serves to limit the list of probable contaminants to a small number. Tentative identifications of some of the contaminants shown as minor peaks in the chromatograms were assigned by matching their retention times (or retention temperatures) with those of probable contaminants. In the case of the six carboxylic acids of Table II, the contaminants are known to be carboxylic acids, since the method of purification involves repeated precipitations as the ammonium salts. The tridecanedioc acid observed in the octadecanedioc acid (compound 10 of Table IV) is considered the source of the lower homolog impurity to-(p-chlorophenyl)-octadecyl bromide (compound 6 of Table IV). [Pg.25]

When all the NaOH is dissolved, add the mixture of bromide compounds, attach the condenser and replace the ice bath by an oil bath. [Pg.231]

A unique 17-electron compound can be prepared by reaction of TaH(CO)4-(dppe) and (Bu C6H4)3C radicals generated from the corresponding bromide compound according to... [Pg.919]

What happens if solid silver bromide is placed in water The solubility table states that bromide compounds are soluble with the exception of silver, lead (II), and mercury (I) ions. Therefore, the silver bromide would be insoluble and remain a solid. [Pg.50]

The only E halide yet reported is [GeBr] , which was made by the gas-phase reaction of Ge atoms and HBr. While the structure of the bromide compound has yet to be determined, it has been used to make GCj R3, clusters (y < x) through the metathesis reaction with sUyl-lithium or sodium reagents as shown in Scheme 13 4M7 formal oxidation state of the Ge... [Pg.5840]

Like other bromide compounds, benzyl bromide corrodes iron and steel and must, therefore, be kept in lead- or enamel-lined containers. It was wfied in battle in small quantities for a short time because its irritant power was much less"than that of other compounds, and its basior I omponent—toluene—was more urgently needed for the manufacture of high explosives. For these reasons, and the fart that chareoal thoroughly absorbs its vapors, it is unlikely that benzyl bromide a ill ever be tt.[Pg.210]

Later, the structure of the trimethylarsine-palladium bromide compound, [ (CH3)3As 2(PdBr2)2], was determined by x-ray crystal analysis (Mann and Wells, 1938) and found to possess the trans symmetric structure, XLIIIB, with a planar molecule 40), It should be added that each of the many bridged compounds prepared in these investigations appeared to be entirely homogeneous in the crystalline state. [Pg.135]

We have seen (Sec. 14.24) that an alkyl halide is conveniently detected by the precipitation of insoluble silver halide when it is warmed with alcoholic silver nitrate. The reaction occurs nearly instantaneously with tertiary, allyl, and benzyl bromides, and within five minutes or so with primary and secondary bromides. Compounds containing halogen joined directly to an aromatic ring or to a doubly-bonded carbon, however, do not yield silver halide under these conditions. Bromo-benzene or vinyl bromide can be heated with alcoholic AgN03 for days without the slightest trace of AgBr being detected. In a similar way, attempts to convert aryl... [Pg.823]

Hello There the mystery photo chem stores were The legends were true. So many chems at super low prices. All manners of bromide compounds, phenyl compounds (including catechol), chromic acids, acids, bases, hydroxylamines(l), iodine, solvents, palladium and platinum compounds. Everything This led me in new search directions to find even more stores. Thanks, bra Here are some addresses ... [Pg.216]

DMTST) to give the tetrasaccharide derivative 99 in 86% yield. Donor 98 was prepared from L-fucose tetraacetate (97) by sequential treatments with methylth-iotrimethylsilane and sodium methoxide in methanol, followed by 0-benzylation by the action of sodium hydride-benzyl bromide. Compound 99 was converted into the glycosyl acceptor 100 (75%) by reductive opening of the benzylidene ring... [Pg.277]

A SF value >1.00 indicates a synergistic interaction and a value < l.(X) indicates an antagonistic interaction while a value of 1.00 would indicate the absence of synergy. Cobalt(II) acetate itself is an autoxidation catalyst [11], as is manganese(II) acetate [11], and as are bromide compounds [12]. Under the mild conditions employed in these... [Pg.1123]

Bromide ions that separate from bromide compounds accelerate the degradation at the gold aluminum junction. [Pg.421]

Surprisingly, the sulfur epimer 60 prepared from ( , )-2,4-hexadiene was found to be unreactive toward phenylmagnesium bromide. Compound 60-reacted with methyUithium to give 57, but the yield was poor. This result was rationalized by considering the conformations of adducts 54 versus 60. Adduct 54 exists as half-chair conformer 54A vide supra). [Pg.19]


See other pages where Bromide compounds is mentioned: [Pg.700]    [Pg.700]    [Pg.90]    [Pg.116]    [Pg.245]    [Pg.91]    [Pg.185]    [Pg.82]    [Pg.110]    [Pg.111]    [Pg.34]    [Pg.198]    [Pg.707]    [Pg.17]    [Pg.81]    [Pg.346]    [Pg.323]    [Pg.1126]    [Pg.215]    [Pg.130]    [Pg.86]    [Pg.34]    [Pg.130]    [Pg.412]    [Pg.276]    [Pg.244]    [Pg.651]   


SEARCH



Alkenyl bromides Grignard compound reactions

Alkyllithium compounds bromides

Aromatic compounds copper bromide

Aryl bromides Grignard compound reactions

Benzyl Bromide reactions with active methylene compounds

Boron bromide compound with

Bromide compounds halide hydrogenolysis

Carbonyl bromides compounds

Copper bromide carbonyl compounds

Copper compounds bromide

Gallium bromide compounds

Graphite, intercalation compounds bromides

Magnesium Compounds Allylmagnesium bromide

Magnesium Compounds Butylmagnesium bromide

Magnesium bromide allylstannane reaction with carbonyl compounds

Organic compounds carbonyl bromide chloride

Phosphonitrile bromide, compound

Phosphonitrile bromide, compound trimeric and tetrameric

Selenenyl bromide, 2-pyridyldehydrogenation carbonyl compounds

© 2024 chempedia.info