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Hydrogenation metal catalyst

Alkenes react mainly by addition. Typical reagents that add to the double bond are halogens, hydrogen (metal catalyst required), water (acid catalyst required), and various acids. If either the alkene or the reagent is symmetrical (Table 3.2), only one product is possible. If both the alkene and reagent are unsymmetrical, however, two products are possible, in principle. In this case, Markovnikov s rule (Secs. 3.8-3.10) allows us to predict the product obtained. [Pg.37]

Metal Catalysts. Transition metals are commonly used as catalysts, particularly in reduction reactions such as hydrogenation. Metal catalysts may be used in bulk form as pure metals, in combination with other metals as bimetallic or multi-metallic mixtures, or may be dispersed on solid supports such as silica, alumina, or carbon (4). The support may influence the reactivity of adsorbed compounds inherent in the structure and morphology of the metal particles dispersed on the support. [Pg.118]

The catalytic hydrogenation of ethylene occurs on various metal catalysts, such as nickel, including active or skeletal forms produced by dissolving out... [Pg.732]

Another possible route to 2-unsubstituted thiazoles is replacement of a mercapto group by a hydrogen. Various methods have been used hydrogen peroxide in acid medium (17-19) dilute nitric acid (17), and metallic catalysts (20-22). [Pg.340]

The uncatalyzed addition of hydrogen to an alkene although exothermic is very slow The rate of hydrogenation increases dramatically however m the presence of cer tain finely divided metal catalysts Platinum is the hydrogenation catalyst most often used although palladium nickel and rhodium are also effective Metal catalyzed addi tion of hydrogen is normally rapid at room temperature and the alkane is produced m high yield usually as the only product... [Pg.231]

The solvent used m catalytic hydrogenation is chosen for its ability to dissolve the alkene and is typically ethanol hexane or acetic acid The metal catalysts are insoluble m these solvents (or indeed m any solvent) Two phases the solution and the metal are present and the reaction takes place at the interface between them Reactions involving a substance m one phase with a different substance m a second phase are called het erogeneous reactions... [Pg.231]

Hydrogenation of alkynes may be halted at the alkene stage by using special catalysts Lindlar palladium is the metal catalyst employed most often Hydrogenation occurs with syn stereochemistry and yields a cis alkene... [Pg.384]

Reduction to alcohols (Section 15 2) Aide hydes are reduced to primary alcohols and ketones are reduced to secondary alcohols by a variety of reducing agents Catalytic hydrogenation over a metal catalyst and reduction with sodium borohydride or lithium aluminum hydride are general methods... [Pg.713]

The intermediate m hydrogenation formed by reaction of the unsaturated ester with the hydrogenated surface of the metal catalyst not only can proceed to the saturated fatty acid ester but also can dissociate to the original ester having a cis double bond or to its trans stereoisomer Unlike polyunsaturated vegetable oils which tend to reduce serum cholesterol levels the trans fats produced by partial hydrogenation have cholesterol raising effects similar to those of saturated fats... [Pg.1074]

Hydrogenation over a metal catalyst such as platinum palladium or nickel... [Pg.1211]

In addition to the processes mentioned above, there are also ongoing efforts to synthesize formamide direcdy from carbon dioxide [124-38-9J, hydrogen [1333-74-0] and ammonia [7664-41-7] (29—32). Catalysts that have been proposed are Group VIII transition-metal coordination compounds. Under moderate reaction conditions, ie, 100—180°C, 1—10 MPa (10—100 bar), turnovers of up to 1000 mole formamide per mole catalyst have been achieved. However, since expensive noble metal catalysts are needed, further work is required prior to the technical realization of an industrial process for formamide synthesis based on carbon dioxide. [Pg.509]

Polymerization and GycliZation. Acetylene polymerizes at elevated temperatures and pressures which do not exceed the explosive decomposition point. Beyond this point, acetylene explosively decomposes to carbon and hydrogen. At 600—700°C and atmospheric pressure, benzene and other aromatics are formed from acetylene on heavy-metal catalysts. [Pg.374]

Hydrogen peroxide may react directiy or after it has first ionized or dissociated into free radicals. Often, the reaction mechanism is extremely complex and may involve catalysis or be dependent on the environment. Enhancement of the relatively mild oxidizing action of hydrogen peroxide is accompHshed in the presence of certain metal catalysts (4). The redox system Fe(II)—Fe(III) is the most widely used catalyst, which, in combination with hydrogen peroxide, is known as Fenton s reagent (5). [Pg.471]

Initially, aluminum chloride was the catalyst used to isomerize butane, pentane, and hexane. Siace then, supported metal catalysts have been developed for use ia high temperature processes that operate at 370—480°C and 2070—5170 kPa (300—750 psi), whereas aluminum chloride and hydrogen chloride are universally used for the low temperature processes. [Pg.207]

High tempeiatuie and high piessuie reactions of MDA with hydrogen in the presence of noble metal catalysts convert 4,4 -MDA into bis(4-aminocyclohexyl)methane (H 2 DA) [1761-71-3] (C22H2gN2). The products ate a mixture of cis and trans isomers that can be controlled to some extent by the proper choice of catalyst and reaction conditions (6—12). [Pg.248]

Nitrile Intermediates. Most quaternary ammonium compounds are produced from fatty nitriles (qv), which are ia turn made from a natural fat or oil-derived fatty acid and ammonia (qv) (Fig. 2) (see Fats AND FATTY oils) (225). The nitriles are then reduced to the amines. A variety of reduciag agents maybe used (226). Catalytic hydrogenation over a metal catalyst is the method most often used on a commercial scale (227). Formation of secondary and tertiary amine side-products can be hindered by the addition of acetic anhydride (228) or excess ammonia (229). In some cases secondary amines are the desired products. [Pg.381]


See other pages where Hydrogenation metal catalyst is mentioned: [Pg.1074]    [Pg.1074]    [Pg.1074]    [Pg.1074]    [Pg.114]    [Pg.1081]    [Pg.106]    [Pg.458]    [Pg.313]    [Pg.1078]    [Pg.366]    [Pg.367]    [Pg.1074]    [Pg.1074]    [Pg.1074]    [Pg.1074]    [Pg.114]    [Pg.1081]    [Pg.106]    [Pg.458]    [Pg.313]    [Pg.1078]    [Pg.366]    [Pg.367]    [Pg.71]    [Pg.2783]    [Pg.231]    [Pg.957]    [Pg.416]    [Pg.422]    [Pg.67]    [Pg.182]    [Pg.241]    [Pg.25]    [Pg.273]    [Pg.374]    [Pg.58]    [Pg.100]    [Pg.465]    [Pg.206]    [Pg.208]    [Pg.208]    [Pg.220]    [Pg.238]    [Pg.238]    [Pg.260]    [Pg.374]   
See also in sourсe #XX -- [ Pg.3 , Pg.4 ]




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