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Halogenations using hydrogen peroxide

Chemical methods, where compatible, shall be used on a wider variety of constmction materials. These methods typically employ oxidizing agents such as halogenated compounds, hydrogen peroxide, ozone. [Pg.70]

Figure 3.108 Halogenation of substituted pyridines using hydrogen peroxide/hydrogen halide systems. Figure 3.108 Halogenation of substituted pyridines using hydrogen peroxide/hydrogen halide systems.
The first chemical oxidation of pyrrole 106 (scheme 26) was achieved as early as 1916 by using hydrogen peroxide to obtain an amorphous powder known as pyrrole black [158]. The room temperature conductivity of PPy 20 prepared with acid or peroxide are in the range of 10"to 10 " S/cm, which can be inereased by halogen doping to 10 S/cm [159]. This low conductivity is due to the high degree of saturation of the pyrrole monomer units caused by defects. In the last... [Pg.49]

The oxidation of thioamides 63 with a wide variety of oxidizing agents is a well-employed method for the synthesis of 3,5-disubstituted-l,2,4-thiadiazoles 64 <1982AHC285>. However, this method is limited mainly to arylthioamides. The most common oxidizing agents tend to be halogens, hydrogen peroxide, dimethyl sulfoxide (DMSO), and nitrous acid. Yields from these reactions are variable and depend on the thioamide, oxidant, and conditions used (Equation 19). By-products such as nitriles and isothiocyanates are usually formed. [Pg.501]

Initial halogenation of the oxime can use chlorine, hypobromite, bromine, or A-bromoacetamide. " Oxidation of the a-halonitrosoalkane can be achieved with nitric acid, nitric acid-hydrogen peroxide, " atmospheric oxygen, ozone, or a peroxyacid. Reduction of thea-halonitroalkaneis achieved with sodium borohydride or by catalytic hydrogenation, although potassium hydroxide in ethanol has been used for the conversion. [Pg.19]


See other pages where Halogenations using hydrogen peroxide is mentioned: [Pg.158]    [Pg.158]    [Pg.166]    [Pg.115]    [Pg.166]    [Pg.59]    [Pg.157]    [Pg.158]    [Pg.166]    [Pg.871]    [Pg.125]    [Pg.125]    [Pg.266]    [Pg.648]    [Pg.222]    [Pg.472]    [Pg.76]    [Pg.314]    [Pg.478]    [Pg.247]    [Pg.1]    [Pg.367]    [Pg.72]    [Pg.603]    [Pg.664]    [Pg.266]    [Pg.219]    [Pg.429]    [Pg.186]    [Pg.189]    [Pg.914]    [Pg.122]    [Pg.73]    [Pg.260]    [Pg.110]    [Pg.121]    [Pg.122]    [Pg.108]    [Pg.160]    [Pg.54]    [Pg.334]    [Pg.10]    [Pg.184]    [Pg.35]    [Pg.297]    [Pg.597]   
See also in sourсe #XX -- [ Pg.259 , Pg.294 ]




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Hydrogen-halogen

Peroxidative halogenations

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