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Chromium bromide, 6-hydrate

C6H2uBr3CrN6 0.6 H2O, Tris(ethylenediamine)chromium(III) bromide hydrate, 45B, 1016... [Pg.464]

The hydroxide is usually converted by acids and salts into chromium tetraphenyl salts,1 the fifth phenyl group being split off as phenol or diphenyl. The amount of phenol formed varies apparently with the previous history of the base, homogeneous chromium pentaphenyl hydroxide in its hydrated form giving a 100 per cent, yield of phenol and only traces of diphenyl when treated with a salt such as potassium bromide in the presence of chloroform. The hydrate in absolute alcohol in the complete absence of air affords one molecule of phenol from each molecule of base when acted upon by potassium iodide. The production of phenol probably occurs according to the scheme... [Pg.262]

Tris(0,0 -diethyl dithiophosphato)-chromium(III), 6 142 Tris (ethylenediamine)chromium-(III) bromide, 4-hydrate, 2 199 Tris (ethylenediamine) chromium-(III) chloride, 3j-hydrate,... [Pg.251]

See other pages where Chromium bromide, 6-hydrate is mentioned: [Pg.63]    [Pg.1020]    [Pg.105]    [Pg.37]    [Pg.220]    [Pg.976]    [Pg.155]    [Pg.31]    [Pg.220]    [Pg.17]    [Pg.1020]    [Pg.183]    [Pg.785]    [Pg.32]    [Pg.712]   
See also in sourсe #XX -- [ Pg.10 , Pg.27 ]

See also in sourсe #XX -- [ Pg.10 , Pg.27 ]



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