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Iron tribromide

Formula FeBrs MW 295.56 Synonym ferric bromide iron tribromide... [Pg.416]

CuSe03 COPPER SELENITE 633 FeBr3 IRON TRIBROMIDE 681... [Pg.1907]

As it approaches the it electron cloud of the alkene, Bt2 becomes temporarily polarized, rendering one of the bromine atoms electrophilic (6+). This bromine atom becomes sufEciendy electrophilic to react with the alkene but is not sufficiently electrophilic to react with benzene. The presence of iron (Fe) in the reaction mixture enhances the electrophilicity of this bromine atom. To understand how iron accomplishes this task, we must recognize that iron itself is not the real catalyst. Rather, it first reacts with Bt2 to generate iron tribromide (FeBr3). [Pg.860]

Iron tribromide, a Lewis acid, is the real catalyst in the reaction between benzene and bromine. Specifically, FeBta interacts with Bt2 to form a complex which reacts as if it were Br. ... [Pg.860]

Iron tribromide is a Lewis acid that interacts with Br2 and generates Br, which is sufficiently electrophilic to be attacked by benzene. [Pg.904]

Predict the major product obtained when each of the following compounds is treated with bromine in the presence of iron tribromide. [Pg.909]

Compound A and compound B are both aromatic esters with molecular formula CsHsOa. When treated with bromine in the presence of iron tribromide, compound A is converted into only one product, while compound B is converted into two different monobromination products. Identify the structure of compound A and compound B. [Pg.911]

Phosphor-athcr, m. phosphoric ether (ester of phosphoric acid, specif, ethyl phosphate), -basis, phosphorus base, -bestimmung, /. determination of phosphorus, -blei, n. lead phosphide Min.) pyromorphite. -bombe, f. phosphorus bomb. -brandgranate, /. phosphorus incendiary shell, -brei, m. phosphorus paste, -bromid, n. phosphorus bromide, specif, phosphorus pentabromide, phos-phorus(V) bromide, -bromijr, n. phosphorus tribromide, phosphorus(III) bromide, -bronze, /. phosphor bronze, -calcium, n. calcium phosphide, -chlorid, n. phosphorus chloride, specif, phosphorus pcntachloride, phosphorus(V) chloride, -chloriir, n. phosphorous chloride (phosphorus trichloride, phosphorus(III) chloride), -dampf, tn. phosphorus vapor or fume, -eisen, n. ferrophos-phorus iron phosphide, -eisensinter, m. diadochite. [Pg.339]

Molybdenum hexafluoride. 3,1412 Molybdenum-iron-sulfur complexes, 4,241 Molybdenum oxide amino acid formation prebiotic systems, 6, 872 Molybdenum storage protein microorganisms, 6, 681 Molybdenum telluride, 3, 1431 Molybdenum tetraalkoxides physical properties, 2, 347 Molybdenum tribromide, 3,1330 Molybdenum trichloride, 3,1330 Molybdenum trifluoride, 3, 1330 Molybdenum trihalides, 3, 1330 bond lengths, 3, 1330 magnetic moments, 3,1330 preparation, 3,1330 properties, 3, 1330 structure, 3,1330 Molybdenum triiodide, 3,1330 Molybdenum trioxide complexes, 3, 1379 Molybdenum triselenide, 3, 143)... [Pg.170]

Reaction of the iron complex salt 602 with the arylamine 921 in the presence of air led directly to the tricarbonyl(ri -4b,8a-dihydro-9H-carbazole)iron complex (923) by a one-pot C-C and C-N bond formation. Demetalation of complex 923 and subsequent aromatization by catalytic dehydrogenation afforded 3,4-dimethoxy-l-heptyl-2-methylcarbazole (924), a protected carbazoquinocin C. Finally, ether cleavage of 924 with boron tribromide followed by oxidation in air provided carbazoquinocin C (274) (640) (Scheme 5.120). [Pg.269]

Aluminum trichloride is the most commonly used catalyst, although aluminum tribromide is more efficient.1 For the rearrangement of l-broino-2-chloro-1,L2-lrifluoroethane (3) to 2-bromo-2-chloro-l,l,l-trifhioroethane (4). none of the following Lewis acids are effective iron(III) chloride. iron(III) bromide, antimony(III) chloride, antimony(V) chloride. tin(IV) chloride, titanium(IV) chloride, zinc(II) chloride, and boron trifluoride-diethyl ether complex.1" ... [Pg.164]

The catalysts used successfully in the liquid phase in the order of their efficiency are anti-niony(V) chloride, aluminum tribromide, aluminum trichloride, and iron(Ill) chloride. Zinc(ll) chloride, tin(ll) chloride, boron trifluoride diethyl ether complex, and aluminum trifluoridc do not catalyze the dismutation. [Pg.289]

Cleavage of the iron complex and the ben/yl ether functions is accomplished with boron tribromide solution. [Pg.175]

Metal Halides. Reacts explosively or violently with the following calcium bromide iron(III) bromide or chloride iron(II) bromide or iodide cobalt(II) chloride silver fluoride all four mercury(II) halides copper(I) chloride, bromide or iodide copper(II) chloride and bromide ammonium tetrachlorocuprate zinc and cadmium chlorides, bromides, and iodides aluminum fluoride, chloride, and bromide thallium bromide tin(II) or (IV) chloride tin(IV) iodide arsenic trichloride and triiodide antimony and bismuth trichlorides, tribromides, and triiodides vanadium(V) chloride chromium(IV) chloride manganese(II) and iron(II) chlorides and nickel chloride, bromide, and iodide.17,22"25... [Pg.485]

By reduction of iron phosphate in hydrogen, or by passing vapours of phosphorus trichloride, tribromide, or tri-iodide over reduced iron at red heat, Granger obtained 12 grey prismatic crystals of composition... [Pg.183]

V. Braun reaction Cyanogen bromide. Phosphorus tribromide. Piperidine. Thionyl chloride. Bromination Aluminum bromide. Aluminum chloride. Boron tribromide. Bromine chloride. N-Bromocaprolactam. N-Bromosuccinimide. Bromotrichloromethane. Cupric bromide. Dibenzoyl peroxide. l,3-Dibromo-5,5-diraethylhydantoin. 1,2-Dibromotetrachloromethane. HBr-scavengers acetamide and potassium chlorate. Iodine. Iodine monobromide. Iron. Mercuric acetate. Phenyl trimethylammonium perbromide. Phosphorus trichloride. Pyridine. Pyridine perbromide. Pyridinium hydrobromide perbromide. Silver sulfate. Sodium acetate. Sodium hypobromite. Sulfur. Sulfur monochloride. Tetramethylaramonium tribromide. M-Tribromoacetophenone. Trichloromethane sulfonyl bromide. Trilluoroacetyl hypobromite. Triphenylphosphine dibromide. [Pg.655]

Bromination Boron tribromide. Bromotrifluoromethane. N-Bromosuccinamide. n-Butyla-mine. Cupric bromide. Dibromoisocyanuric acid. Dioxane dibromide. Iodine monobromide. Iron. Pyridine. [Pg.240]


See other pages where Iron tribromide is mentioned: [Pg.254]    [Pg.681]    [Pg.642]    [Pg.642]    [Pg.254]    [Pg.681]    [Pg.642]    [Pg.642]    [Pg.85]    [Pg.1726]    [Pg.130]    [Pg.151]    [Pg.275]    [Pg.308]    [Pg.222]    [Pg.1033]    [Pg.1806]    [Pg.1726]    [Pg.188]    [Pg.127]    [Pg.1001]    [Pg.593]    [Pg.991]    [Pg.554]    [Pg.1726]    [Pg.188]    [Pg.328]    [Pg.418]    [Pg.420]    [Pg.798]    [Pg.934]    [Pg.485]   
See also in sourсe #XX -- [ Pg.2 , Pg.415 ]

See also in sourсe #XX -- [ Pg.182 ]

See also in sourсe #XX -- [ Pg.254 ]




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