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Hydrogen stepwise

There is an indication in a number of studies that benzene is hydrogenated stepwise through cyclohexene see, for example, the quantitative explanation by Wei and Prater (214) of Smith s results, in which hydrogenation of benzene produced a small quantity, namely, 0.0051 mole % of cyclohexene. Hartog et al. (215) obtained similar results. Tetenyi, et al. (216) come to the conclusion on the basis of kinetic data that cyclohexane dehydrogenates stepwise, through cyclohexene. [Pg.46]

Hydrogenation. Cyclopentadiene can be hydrogenated stepwise through cyclopentene to cyclopentane in the presence of hydrogen and noble metal catalysts such as palladium (2). The heats of reaction at 82°C are as follows (28) ... [Pg.2070]

Hydrogenation of methylbutynol gives 2-methyl-3-buten-2-ol and then 2-methylbutan-2-ol in stepwise fashion (192). [Pg.113]

Multiply unsaturated linolenic and linoleic acid residues make triglycerides more vulnerable to oxidative degradation than oleic acid which is relatively stable. It is therefore desirable to hydrogenate the most unsaturated residues selectively without production of large quantities of stearic (fully saturated) acid. The stepwise reduction of an unsaturated oil may be visualized as ... [Pg.125]

Reactions and Uses. The common reactions that a-hydroxy acids undergo such as self- or bimolecular esterification to oligomers or cycHc esters, hydrogenation, oxidation, etc, have been discussed in connection with lactic and hydroxyacetic acid. A reaction that is of value for the synthesis of higher aldehydes is decarbonylation under boiling sulfuric acid with loss of water. Since one carbon atom is lost in the process, the series of reactions may be used for stepwise degradation of a carbon chain. [Pg.517]

Animal metaboHsm is based on the reactions of oxygen and organic compounds containing carbon, hydrogen, oxygen, and nitrogen and other heteroatoms. Enzymes catalyze these biochemical oxidations, which are accompHshed at about 30—40°C and frequendy proceed stepwise to produce... [Pg.476]

Another subclass of substituted amides that is of great commercial value is the ethoxylated amides. They can be synthesized from alkanolamides by chain extending with ethylene or propylene oxide or by ethoxylation directly from the primary amide (46—48). It was originally beheved that the stepwise addition of ethylene oxide (EO) would produce the monoethano1 amide and then the diethanolamide when sufficient ethylene oxide was added (49), but it has been discovered that only one hydrogen of the amide is substituted with ethylene oxide (50—53). As is typical of most ethylene oxide adducts, a wide distribution of polyethylene oxide chain length is seen as more EO is added. A catalyst is necessary to add ethylene oxide or propylene oxide to a primary or an ethoxylated amide or to ethoxylate a diethoxy alkanolamide synthesized from diethanolamine (54). [Pg.184]

Tin tetrachloride has been used to prepare the stericaHy hindered triisopropylchlorosilane [13154-24-0] (119). Organobromosdanes are obtained under similar conditions through reaction with cupric and mercuric bromide. These reactions are most suitable for stepwise displacement of hydrogen to form mixed hydridochlorosilanes or in systems sensitive to halogen (120). Hydrides have also been displaced using organic bromides. Heating triethylsilane and... [Pg.27]

Reduction to Metal Powder. The metal powder is obtained from APT by stepwise reduction with carbon or hydrogen. The intermediate products are the yeUow oxide, WO blue oxide, (see Tungsten compounds) and brown oxide, WO2. Because carbon introduces impurities,... [Pg.281]

Since both complete hydrogenation of acetylene or any hydrogenation of the ethylene results in the production of a less valuable product such as ethane, conditions must be chosen carefiiUy and a catalyst must be used that is both sufficiently active for acetylene hydrogenation and extremely selective to avoid ethylene hydrogenation. Since hydrogenation of acetylenic bonds proceeds stepwise and since acetylene is more strongly adsorbed on the catalytic... [Pg.199]

In oiological systems, the most frequent mechanism of oxidation is the remov of hydrogen, and conversely, the addition of hydrogen is the common method of reduc tion. Nicotinamide-adenine dinucleotide (NAD) and nicotinamide-adenine dinucleotide phosphate (NADP) are two coenzymes that assist in oxidation and reduction. These cofactors can shuttle between biochemical reac tions so that one drives another, or their oxidation can be coupled to the formation of ATP. However, stepwise release or consumption of energy requires driving forces and losses at each step such that overall efficiency suffers. [Pg.2133]

The formation of a single complex species rather than the stepwise production of such species will clearly simplify complexometric titrations and facilitate the detection of end points. Schwarzenbach2 realised that the acetate ion is able to form acetato complexes of low stability with nearly all polyvalent cations, and that if this property could be reinforced by the chelate effect, then much stronger complexes would be formed by most metal cations. He found that the aminopolycarboxylic acids are excellent complexing agents the most important of these is 1,2-diaminoethanetetra-aceticacid (ethylenediaminetetra-acetic acid). The formula (I) is preferred to (II), since it has been shown from measurements of the dissociation constants that two hydrogen atoms are probably held in the form of zwitterions. The values of pK are respectively pK, = 2.0, pK2 = 2.7,... [Pg.55]

Solochrome dark blue or calcon ( C.1.15705). This is sometimes referred to as eriochrome blue black RC it is in fact sodium l-(2-hydroxy-l-naphthylazo)-2-naphthol-4-sulphonate. The dyestuff has two ionisable phenolic hydrogen atoms the protons ionise stepwise with pK values of 7.4 and 13.5 respectively. An important application of the indicator is in the complexometric titration of calcium in the presence of magnesium this must be carried out at a pH of about 12.3 (obtained, for example, with a diethylamine buffer 5 mL for every 100 mL of solution) in order to avoid the interference of magnesium. Under these conditions magnesium is precipitated quantitatively as the hydroxide. The colour change is from pink to pure blue. [Pg.318]


See other pages where Hydrogen stepwise is mentioned: [Pg.522]    [Pg.198]    [Pg.202]    [Pg.43]    [Pg.48]    [Pg.411]    [Pg.129]    [Pg.522]    [Pg.198]    [Pg.202]    [Pg.43]    [Pg.48]    [Pg.411]    [Pg.129]    [Pg.45]    [Pg.330]    [Pg.115]    [Pg.335]    [Pg.343]    [Pg.44]    [Pg.133]    [Pg.175]    [Pg.456]    [Pg.311]    [Pg.315]    [Pg.177]    [Pg.572]    [Pg.26]    [Pg.291]    [Pg.305]    [Pg.153]    [Pg.621]    [Pg.382]    [Pg.313]    [Pg.232]    [Pg.107]    [Pg.25]    [Pg.55]    [Pg.202]    [Pg.77]    [Pg.163]    [Pg.164]    [Pg.268]    [Pg.270]    [Pg.771]   
See also in sourсe #XX -- [ Pg.352 ]

See also in sourсe #XX -- [ Pg.152 , Pg.159 , Pg.161 , Pg.182 , Pg.185 ]




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Stepwise hydrogenation

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