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Monoxide tetrabromide

Alkenes, alkynes, and arenes, e.g., ethylene, acetylene and benzene, respectively, react (1) with bromine by addition, e.g., ethylene dibromide C HiBri (1.2). acetylene tetrabromide C2H .Br4 1,1,2,2. hexabromocyclo-hexane QHgBr also carbon monoxide yields carbonyl bromide COBr2i (2) with hypobromous add by addition. e.g., olefins form, for example,... [Pg.259]

Carbon monoxide, 111, 252, 393-394, 465 Carbon oxysulfide, 112-113 Carbon tetrabromide-tin(ll) fluoride, 111-112 1,1 -Carbonylbis(3-imidazolium)bismethane-sulfonate, 112... [Pg.332]

Carbon disulfide captan, dazomet, dithianon, EXD, ferbam, folpet, hexythiazox, isoprothioiane, mancozeb, maneb, metam, methidathion, nabam, propineb, tebuthiuron, thicyofen, thiram, zineb, ziram Carbon monoxide fenuron Carbon oxy sulfide see carbonyl sulfide Carbon tetrabromide deltamethrin, tralomethrin Carbon tetrachloride cypermethrin, permethrin, tridiphane... [Pg.1028]

The transfer of halide from 7r-allylnickel halide to aluminum to give a haloaluminum anion results in a strong decrease in the electron density and formation of free coordination positions on nickel. The presence and number of free coordination positions can be demonstrated by reaction with carbon monoxide. The catalytically active complex, XIII, reacts at —40°C. with 2 moles of carbon monoxide to give the inactive XIV which can be isolated. In XIII, there are accordingly two free coordination positions. During catalysis, these positions are presumably occupied by olefins in the form of 7r-complexes. A stable olefin 7r-complex, 7r-allylnickel (7T-cycloocta-l,5-diene) aluminum tetrabromide, XV, can actually be isolated by adding cycloocta-l,5-diene to a solution of the active complex, XIII. [Pg.259]

Carbonothioic acid, 0-(6-chloro-3-phenyl-4-pyridazinyl) S-octyl ester. See Pyridate, Carbonothioic dichloride. See Thiophosgene Carbon oxide. See Carbon monoxide Carbon oxide sulfide. See Carbonyl sulfide Carbon oxychloride. See Phosgene Carbon oxysulfide. See Carbonyl sulfide Carbon silicide. See Silicon carbide Carbon sulfide. See Carbon disulfide Carbon tet. See Carbon tetrachloride Carbon tetraboride. See Boron carbide Carbon tetrabromide CAS 558-13-4 EINECS/ELINCS 209-189-6 UN 2516... [Pg.768]

Write a formula for each molecular compoimd. (a) carbon monoxide (b) disulfur tetrafluoride (c) dichlorine monoxide (d) phosphorus pentafluoride (e) boron tribromide (f) diphosphorus pentasulfide 74. Write a formula for each molecular compound. (a) chlorine monoxide (b) xenon tetroxide (c) xenon hexafluoride (d) carbon tetrabromide (e) diboron tetrachloride (f) tetraphosphorus triselenide... [Pg.157]


See other pages where Monoxide tetrabromide is mentioned: [Pg.575]    [Pg.457]    [Pg.28]    [Pg.575]    [Pg.201]    [Pg.109]    [Pg.260]    [Pg.575]    [Pg.2998]    [Pg.147]    [Pg.260]    [Pg.60]    [Pg.575]    [Pg.644]    [Pg.71]    [Pg.912]    [Pg.244]    [Pg.75]    [Pg.3383]    [Pg.1604]   
See also in sourсe #XX -- [ Pg.222 ]




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Tetrabromide

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