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Oxygen-nitrogen derivatives phenols

Acetamide ( C2H5ON ) + Pyrocatechol ( CjHtOg ) Kremann and Auer, 1918 [Pg.915]

Succininide ( C,HsOgN ) + m-Nitrophenol ( CsHjOjN ) Krenann and Dietrich, 1923 [Pg.930]

Succinimide ( CuH50gN ) Kremann and Dietrich, + 2,3-Dioxynaphthalene ( CioHbOs ) 1923  [Pg.931]

Sarcosin anhydride ( C H,oOgNa ) + Resacetophe-none ( CeHgOs ) [Pg.942]

Sarcosin anhydride phenone ( C,aH,oOa Pfeiffer and Wang, ( C HioOgWa ) 1927 ) + 2,5-Dloxybenzo- [Pg.942]

Chemical/Physical. In an environmental chamber, nitrogen trioxide (10,000 ppb) reacted quickly with phenol (concentration 200 ppb to 1.4 ppm) to form phenoxy radicals and nitric acid (Carter et al., 1981). The phenoxy radicals may react with oxygen and nitrogen dioxide to form quinones and nitrohydroxy derivatives, respectively (Nielsen et al, 1983). [Pg.953]

See other pages where Oxygen-nitrogen derivatives phenols is mentioned: [Pg.914]    [Pg.914]    [Pg.389]    [Pg.187]    [Pg.106]    [Pg.749]    [Pg.743]    [Pg.434]    [Pg.642]    [Pg.936]    [Pg.77]    [Pg.122]    [Pg.105]    [Pg.22]    [Pg.347]    [Pg.187]    [Pg.108]    [Pg.229]    [Pg.367]    [Pg.322]    [Pg.157]    [Pg.424]    [Pg.157]    [Pg.341]    [Pg.420]    [Pg.418]    [Pg.104]    [Pg.87]    [Pg.443]    [Pg.493]    [Pg.377]    [Pg.329]    [Pg.91]    [Pg.108]    [Pg.62]    [Pg.77]    [Pg.57]    [Pg.7]    [Pg.381]    [Pg.95]    [Pg.231]    [Pg.388]    [Pg.26]    [Pg.1069]    [Pg.1493]    [Pg.858]    [Pg.606]    [Pg.98]    [Pg.172]    [Pg.205]   


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Nitrogen derivatives

Nitrogen derivatives phenols

Nitrogenous Derivatives

Oxygen derivation

Oxygen derivatives

Oxygen phenol

Oxygen phenolic

Oxygenation, phenol

Phenolic derivatives

Phenols derivs

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