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Density conjugate

The condensation of aldehydes or ketones with secondary amines leads to "encunines via N-hemiacetals and immonium hydroxides, when the water is removed. In these conjugated systems electron density and nudeophilicity are largely transferred from the nitrogen to the a-carbon atom, and thus enamines are useful electroneutral d -reagents (G.A. Cook, 1969 S.F. Dyke, 1973). A bulky heterocyclic substituent supports regio- and stereoselective reactions. [Pg.13]

In Figure 1, the pairs (or triad) of phases that form ia the various multiphase regions of the diagram are illustrated by the corresponding test-tube samples. Except ia rare cases, the densities of oleic phases are less than the densities of conjugate microemulsions and the densities of microemulsions are less than the densities of conjugate aqueous phases. Thus, for samples whose compositions He within the oleic phase-microemulsion biaodal, the upper phase (ie, layer) is an oleic phase and the lower layer is a microemulsion. For compositions within the aqueous phase-microemulsion biaodal, the upper layer is a microemulsion and the lower layer is an aqueous phase. When a sample forms two layers, but the amphiphile concentration is too low for formation of a middle phase, neither layer is a microemulsion. Instead the upper layer is an oleic phase ("oil") and the lower layer is an aqueous phase ("water"). [Pg.148]

Iron, cobalt, and nickel catalyze this reaction. The rate depends on temperature and sodium concentration. At —33.5°C, 0.251 kg sodium is soluble in 1 kg ammonia. Concentrated solutions of sodium in ammonia separate into two Hquid phases when cooled below the consolute temperature of —41.6°C. The compositions of the phases depend on the temperature. At the peak of the conjugate solutions curve, the composition is 4.15 atom % sodium. The density decreases with increasing concentration of sodium. Thus, in the two-phase region the dilute bottom phase, low in sodium concentration, has a deep-blue color the light top phase, high in sodium concentration, has a metallic bronze appearance (9—13). [Pg.162]

Values for the tt-electron densities in imidazole and two related ions are given in Figure 1, The TT-electron densities in the conjugate acid of imidazole are greater at the 2-position... [Pg.5]

Figure 1 The tt-electron densities in imidazole, its conjugate acid and base, and pyrazole... Figure 1 The tt-electron densities in imidazole, its conjugate acid and base, and pyrazole...
The reactivities of 1-methylpyrazole (33) and pyrazole (29) are similar and so are the corresponding charges. The competition between C-4 and C-4 in 1-phenylpyrazole depends on the electrophile and on the experimental conditions (Section 4.04.2.3.10(i)). Thus in an acidic medium the reaction takes place on the conjugate acid (34) and considering the calculated charge densities the attack on C-4 would always be favoured. [Pg.174]

LIPOPROTEINS. Blood plasma lipoproteins are prominent examples of the class of proteins conjugated with lipid. The plasma lipoproteins function primarily in the transport of lipids to sites of active membrane synthesis. Serum levels of low density lipoproteins (LDLs) are often used as a clinical index of susceptibility to vascular disease. [Pg.126]


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See also in sourсe #XX -- [ Pg.28 ]




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