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Directed hydrogenation

With the lowest ranked group (hydrogen) directed away from us we see that the order of decreasing sequence rule precedence is clockwise The absolute configuration is R... [Pg.292]

Nor IS the hydrogen directly attached to the carbonyl group m aldehydes affected Only the a hydrogen is replaced... [Pg.757]

DEPT (Section 13 18) Abbreviation for distortionless enhance ment of polarization ttansfer DEPT is an NMR technique that reveals the number of hydrogens directly attached to a carbon responsible for a particular signal... [Pg.1281]

Direct Hydrogenation. Direct hydrogenation of lignitic and other coals has been studied by many investigators. Lignite can be slurried with an anthracene-oil solvent, heated to a temperature of 460—500°C with 1 1 CO H2 synthesis gas at pressures to 28 MPa (280 atm) in a 2 kg/h reactor. The product hquids are separated, and in a commercial process, a suitable hydrogen-donor solvent would be recycled (54). [Pg.160]

A second isomer of [10]annulene (the cis, trans, cis, cis, trans stereoisomer) can have bond angles close to 120° but is destabilized by a close contact between two hydrogens directed toward the interior of the ring. To minimize the van der Waals strain between these hydrogens, the ring adopts a nonplanai geometry, which limits its ability to be stabilized by tt electron delocalization. It, too, has been prepared and is not very stable. Similarly, the next higher (4n + 2) system, [14]annulene, is also somewhat destabilized by van der Waals strain and is nonplanar-. [Pg.455]

Mercury has a characteristic ability to form not only conventional ammine and amine complexes but also, by the displacement of hydrogen, direct covalent bonds to nitrogen, e.g. ... [Pg.1218]

Diesters of phosphorous acid are in general neutral because the phosphorous acid exists mostly in the phosphonate form with one hydrogen directly attached to the phosphorus. But with alkali metals the H can be changed against the alkali and reactive intermediates formed. Such alkali metal derivatives of dialkyl phosphites react with alkyl halides to give dialkyl alkanephosphonates, according to Eqs. (45) and (46). [Pg.570]

For a review of homogeneous hydrogenation directed to only one face of a substrate molecule, see Brown, J.M. Angew. Chem. Int. Ed. Engl., 1987, 26, 190. [Pg.1110]

In the dehydration of (44) In acid, a mixture of alkenes was formed which was hydrogenated directly to (41). [Pg.284]

The lactone (59) is made by the method described on page T 96. Addition of the protected acetylene (61) gives the hemlacetal (62) which can be hydrogenated directly to (63). Cyclisation occurs as soon as the protecting group is removed. [Pg.301]

In principle biomass is a useful fuel for fuel cells many of the technologies discussed above for using biomass as a fuel produce either methane or hydrogen directly and as highlighted below synthesis gas production from biomass for conversion to methanol is an attractive option. Cellulose-based material may be converted to a mixture of hydrogen (70% hydrogen content recovered), CO2 and methane by high-temperature treatment with a nickel catalyst. [Pg.180]

Spectroscopic evidence that ethylene preferably hydrogenates directly via the jt-bonded adsorbate and not via the more stable di-<7 bonded state has been provided by Somorjai and coworkers by in situ sum-frequency generation measurements [P.S. Cremer, X. Su, Y.R. Shen and G.A. Somorjai,y. Am. Chem. Soc. 118 (1996) 2942]. [Pg.260]

CO in the synthesis gas mixture for the methanol synthesis does not seem to take part directly in the reaction, but it does influence the process through two effects First the water-gas shift reaction and, secondly, through its effect on the surface morphology (and possibly also composition). For thermodynamic reasons, however, it would be desirable if CO could be hydrogenated directly via Eq (18) instead of going through two coupled equations (3) and (19), since it would yield a higher equilibrium concentration of methanol at the reactor exit. [Pg.319]

In this chapter, the definitions used by Perrin in his book on pA a prediction (which also includes a very convenient compilation of o values) will be used. One must be alert to the importance of the number of hydrogens directly attached to the carbonyl carbon several groups have pointed out that aldehydes and ketones give separate but parallel lines, with formaldehyde displaced by the same amount again. What this means is that given one equilibrium constant for an aldehyde (or ketone) one may estimate the equilibrium constant for other aldehydes (or ketones) from this value and p for the addition using a value from experiment, if available, or estimated if necessary. This assumes that there is no large difference in steric effects between the reference compound and the unknown of interest. [Pg.12]

Hydroxymethyl ati on of Polybutadiene - The hydroformyl ated PBD reaction solution obtained above was subsequently hydrogenated directly using the following reaction conditions Hydroformyl ated PBD solution = 75 ml, RuC1H(C0)(P(CcHc)3)3 = 1.05 mol/m3, Hydrogen pressure = 600 psig, Temperature = 1 0 C. [Pg.398]

In addition to the use of hydrogen directly, hydrogen generated from CO and water (water-gas shift reaction) is also very effective in hydrogenating activated alkenes under basic conditions (Eq. 10.3).5... [Pg.313]

In principle, different reference electrodes may be used if the cell is provided with a separate compartment and a Luggin capillary. But if the flow cell technique is to be applied, it is more convenient to avoid the use of capillaries where the solution cannot be easily exchanged. Active bulk components could diffuse through the capillary and give rise to erroneous responses. A small palladium gauze charged with hydrogen directly immersed in the solution can be used as the reference electrode (PdH ) [18]. [Pg.132]

In the case of hydrogen, direct experimental answers have been scarce, because hydrogen has turned out to be very difficult to observe as an isolated impurity. Fortunately, a large amount of information has been... [Pg.601]

Hydrane A coal gasification process in which coal is hydrogenated directly to methane, using hydrogen gas under pressure, preheated to a high temperature. Developed by the U.S. Bureau of Mines as of 1980 it had not been fully piloted. [Pg.136]

Fuel cells are the cleanest and most efficient technologies for generating electricity from fossil fuels. Since there is no combustion, fuel cells do not produce any of the pollutants commonly emitted by boilers and furnaces. For systems designed to consume hydrogen directly, the only products are electricity, water and heat. [Pg.188]

In the charge, or electrolysis mode, the process splits water into hydrogen and oxygen and can produce hydrogen directly without mechanical compression. Water enters the cell and is split at the surface of the membrane to form protons, electrons and gaseous oxygen. [Pg.205]

Fuel cells typically use hydrogen directly, mostly as compressed gas, possibly also as liquid hydrogen stored on board. Even though the C02-equivalent emissions were assessed to be low, methanol from farmed wood as a fuel for fuel cells turned out to be no optimum solution. The reason is not revealed by the WTW graph. Industry has decided against methanol as a fuel-cell fuel for two reasons ... [Pg.226]

The flavin adenine dinucleotide (FAD) and NADH deliver electrons and hydrogen directly to the respiratory cytochromes whilst acetyl-CoA enters the TCA cycle. [Pg.251]


See other pages where Directed hydrogenation is mentioned: [Pg.292]    [Pg.206]    [Pg.1448]    [Pg.553]    [Pg.427]    [Pg.134]    [Pg.553]    [Pg.534]    [Pg.395]    [Pg.566]    [Pg.1425]    [Pg.1536]    [Pg.305]    [Pg.395]    [Pg.200]    [Pg.44]    [Pg.207]    [Pg.341]    [Pg.17]    [Pg.114]    [Pg.369]    [Pg.197]    [Pg.327]    [Pg.512]    [Pg.382]   
See also in sourсe #XX -- [ Pg.142 ]

See also in sourсe #XX -- [ Pg.584 ]




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Activated imine direct asymmetric hydrogenation

Asymmetric direct hydrogenation

Brown coal direct hydrogenation

Carbon-13 hydrogen direct coupling

Carbon-13 hydrogen direct coupling constants

Catalytic kinetic resolution and directed hydrogenation

Coal liquefaction direct hydrogenation

Direct Hydrogen Cyanide Synthesis

Direct Hydrogen Cyanide Synthesis and Water-gas Shift Reaction

Direct Hydrogen PEFC Systems

Direct Hydrogen Production

Direct Millisecond Hydrogen Exchange

Direct Oxidation of Benzene to Phenol with Hydrogen Peroxide

Direct Solar Thermal Hydrogen Processes

Direct carbon-hydrogen bond functionalizations

Direct dyes hydrogen bonds with cellulose

Direct hydrogen abstraction

Direct hydrogen abstraction mechanism

Direct hydrogen abstraction regioselectivity

Direct hydrogen abstraction stereoselective

Direct hydrogen peroxide synthesis

Direct hydrogenation

Direct hydrogenation mechanism

Direct hydrogenation reactions

Direct hydrogenation, alkene

Direct oxidation of hydrogen

Direct pressurized oxidation of methane to methanol with hydrogen peroxide

Direct synthesis of hydrogen peroxide

Directed reactions hydrogenation, heterogenous

Directional Dependence of Hydrogen Bonding

Directive hydrogenation

Directive hydrogenation

Elimination, direction hydrogen cyanide

Elimination, direction hydrogen)

Ester Unit- or Amide-Directive Hydrogenation

Fatty acids direct hydrogenation

Groups hydrogen-bond-directing

Halogen atoms direct reactions with hydrogen halides

Heteroatom-directed carbon-hydrogen

Hydrogen atoms, direct transfer

Hydrogen bond directional nature

Hydrogen bond, directional influence

Hydrogen bonding direct perturbation

Hydrogen bonds directional

Hydrogen bromide by direct combination over platinized silica gel

Hydrogen chloride direct synthesis

Hydrogen cyanide conjugate vs. direct addition

Hydrogen direct analysis

Hydrogen direct methanol fuel cell

Hydrogen direct synthesis

Hydrogen storage direct

Hydrogen sulfide direct conversion

Hydrogen tunnelling direct dynamics approach

Hydrogen-bond directed assembly

Hydrogenation substituent directive effects

Hydrogenation, catalytic substituent directive effects

Hydrogenation, homogeneous, directed

Hydroxy-directive hydrogenation

Molecular self-assembly, directional hydrogen bonding

Plasma and Directed Ion Beam Hydrogenation Methods

Proton exchange membrane direct hydrogen

Reactions with direct transfer of hydrogen between nicotinamide coenzyme and substrate

SEQUENCE-SPECIFIC HYDROGEN BONDED UNITS FOR DIRECTED ASSOCIATION, ASSEMBLY, AND LIGATION

Site-directed mutagenesis hydrogen bonding

Substrate-Directive Diastereoselective Hydrogenation

Substrate-directive hydrogenation

Theory of Direct Solar Thermal Hydrogen Generation

Vehicle direct hydrogen-fuel-cell-powered

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