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Covalent hydrates hydrogen exchange

Pyrimidin-2-one exchanges its 5-hydrogen much faster than pyridin-2-one. However, this is due to the existence of a small proportion of the covalent hydrate (106) which undergoes rapid exchange. [Pg.189]

Covalent hahdes can be prepared by various synthetic routes. The simplest are direct reactions of elemental halogens (equation 9), or hydrogen halides with elements (equation 10) or oxides (equation 11). In other processes, the oxides are reacted with a halogen halide in the presence of carbon to combine with the oxygen (equation 12) or other reactive carbon-halides (equation 13). Exchange of halogens can also take place (equations 14 16). Anhydrous halides can also be obtained by dehydration of metal halide hydrates, using reactants such as thionyl halide, which react with the hydrated water (equation 17). [Pg.743]


See other pages where Covalent hydrates hydrogen exchange is mentioned: [Pg.196]    [Pg.328]    [Pg.196]    [Pg.386]    [Pg.204]    [Pg.4519]    [Pg.581]    [Pg.711]    [Pg.4518]    [Pg.316]    [Pg.344]    [Pg.333]   
See also in sourсe #XX -- [ Pg.26 , Pg.47 ]




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