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Hydrogenation, general

Table 3 provides typical specifications for isoprene that are suitable for Al—Ti polymerization (89). Traditional purification techniques including superfractionation and extractive distillation are used to provide an isoprene that is practically free of catalyst poisons. Acetylenes and 1,3-cyclopentadiene are the most difficult to remove, and distillation can be supplemented with chemical removal or partial hydrogenation. Generally speaking distillation is the preferred approach. Purity is not the main consideration because high quaUty polymer can be produced from monomer with relatively high levels of olefins and / -pentane. On the other hand, there must be less than 1 ppm of 1,3-cyclopentadiene. [Pg.467]

The addition is therefore stereospecifically syn and, like catalytic hydrogenation, generally takes place from the less-hindered side of a double bond, though not much discrimination in this respect is observed where the difference in hulk effects is small.Diimide reductions are most successful with symmetrical multiple bonds (C=C, C=C, N=N) and are not useful for those inherently polar (C=N, C=N, C=0, etc.). Diimide is not stable enough for isolation at ordinary temperatures, though it has been prepared as a yellow solid at — 196°C. [Pg.1007]

The fact that aryl groups migrate, but alkyl groups and hydrogen generally do not, leads to the proposition that 40, in which the odd electron is not found in the three-membered ring, may be an intermediate. There has been much controversy on this... [Pg.1390]

Rhodium species in oxidation states I and III are involved in the process. Rhodium-catalyzed hydrogenations generally involve oxidative addition reactions, followed by the reverse process of reductive elimination in the final step. Another common elimination process is the so-called (l-elimination, which accounts for the frequent side reaction of isomerization of alkenes, according to Eq. (1) ... [Pg.11]

Catalytic Hydrogenation. General statements about catalytic hydrogenation are difficult to make since the results are affected by many factors such as the catalysts, activators, inhibitors, solvents, pH of the medium, temp, and pressure. [Pg.33]

H2-H2. In contrast to the case of unmixed rare gases, pure molecular gases like hydrogen generally absorb radiation in the far infrared (and elsewhere) as is shown, for example, in Fig. 3.10, for three temperatures [37]. The data shown in the figure were obtained at gas densities from 10 to 100 amagats, but when the measured absorption coefficients are... [Pg.81]

The solution spectrum of pyrrole displays a strong band at ca. 210 nm (Table 23). The weak band at ca. 240 nm reported in the older literature is now generally accepted as arising from autoxidation products. Substitution of methyl for hydrogen generally leads to... [Pg.177]

Alkyl halides with (3-hydrogens generally undergo only elimination reactions under the conditions of the vinyl substitution (100 C in the presence of an amine or other base). Exceptions are known only in cases where intramolecular reactions are favorable. Even alkyl halides without (3-hydrogens appear not to participate in the intermolecular alkene substitution since no examples have been reported, with the exception of reactions with benzyl chloride and perfluoroalkyl iodides. [Pg.842]

Nonbonded electrons are / v / usually not shown in condensed structures. Atoms in organic molecules (except hydrogen) generally obey the octet rule, so any atom with fewer than four bonds must have a number of non-bonded electron pairs equal to four minus the number of bonds. For example, the oxygen in an alcohol has 4 — 2 = 2 nonbonded electron pairs. [Pg.1007]

Three-bond coupling to vicinal hydrogens generally leads to a pentet signal, meaning that coupling to the equatorial fluorines of the SF5 substituent, as mentioned earlier, is much greater than to its axial fluorine. [Pg.293]

In the reduction of pyridine and quinoline compounds, hydrogenation generally occurs.2... [Pg.64]

Esters with only one a hydrogen generally give poor yields in the Claisen condensation. Propose a mechanism for the Claisen condensation of ethyl isobutyrate, and explain why a poor yield is obtained. [Pg.1072]


See other pages where Hydrogenation, general is mentioned: [Pg.257]    [Pg.88]    [Pg.285]    [Pg.232]    [Pg.484]    [Pg.235]    [Pg.38]    [Pg.429]    [Pg.576]    [Pg.384]    [Pg.1008]    [Pg.488]    [Pg.36]    [Pg.97]    [Pg.175]    [Pg.295]    [Pg.232]    [Pg.88]    [Pg.354]    [Pg.212]    [Pg.461]    [Pg.834]    [Pg.329]    [Pg.255]    [Pg.282]    [Pg.113]    [Pg.207]    [Pg.120]    [Pg.225]    [Pg.1784]    [Pg.158]    [Pg.176]    [Pg.100]    [Pg.299]   


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