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Hydrogen atom formation

The total yield of hydrogen under the conditions of these measurements was about 1.6 molecules/100 e.v. If one-half resulted from the primary dissociation also leading to acetylene ion, a yield of 0.8 acetylene ions/100 e.v. may be estimated. This value is a minimum since acetylene ion production can also be accompanied by hydrogen atom formation and is highly uncertain but consistent with the mass spectral fragmentation pattern of acetylene and W which lead to an estimate of ca. 0.94 acetylene ions/100 e.v. [Pg.265]

Hydrogen atoms, formation of bonding moleoular orbital... [Pg.27]

Reactions of the Electrons Radiation-Induced Hydrogen Atom Formation in Frozen Aqueous Solutions... [Pg.188]

With Na2S04, Na2HP04, NasP04, and Na2C08 as solutes where the mechanism of hydrogen atom formation and stabilization is different, the observed linear dependence of the H atom yields of the solute concentration is as expected on the basis of the proposed mechanism. Thus, since the probability of forming an H,OH radical pair in the hydration shell of the anion (—e.g., by dissociation of an excited water molecule) would be proportional to the anion concentration, and sigce the stabilization of the H atom is postulated as the result of the reaction of the OH radical with the anion in whose hydration shell it is formed, it follows that the yield should be proportional to the solute concentration. [Pg.200]

All these contributions add up to a total antihydrogen formation cross section of approximately 2 x 10-15 cm2 in the antiproton energy range 2-10 keV where the charge-exchange production mechanism is likely to be most effective. This value is consistent with results obtained by Ermolaev, Bransden and Mandal (1987), who used the classical trajectory Monte Carlo method, and also with the results of a recent experiment (Merrison et al., 1997) which measured the hydrogen atom formation cross section via reaction (8.22). [Pg.380]

We perform numerical modeling of atomic processes in various real plasmas including LHD fuel-pellet ablation and short-pulse laser interaction plasmas [21], We are developing a mixed quantum-classical code to study excited hydrogen atom formation in neutrals of back scattered protons at wall surfaces. [Pg.382]

Cathodic poisons are substances that interfere with the cathodic reduction reactions, i.e., hydrogen atom formation and hydrogen gas evolution. The rate of the cathodic reaction is slowed, and because anodic and cathodic reactions must proceed at the same rate, the whole corrosion process is slowed. [Pg.131]

Because the neutron tool responds to hydrogen it can be used to differentiate between gas and liquids (oil or water) in the formation. A specific volume of gas will contain a lot fewer hydrogen atoms than the same volume of oil or water (at the same pressure), and therefore in a gas bearing reservoir the neutron porosity (which assumes the tool is... [Pg.146]

Because of its free format, the input tile for TINKER is easier to construct by hand than the input tile for Program MM3. Place the hydrogen atoms at plausible disUitices from the carboti atoms to produce two input files for determining the... [Pg.148]

Only esters containing two a-hydrogen atoms (ethyl acetate, propionate, n-butyrate, etc.) can be condensed with the aid of sodium alkoxides. For esters with one a-hydrogen atom, such as ethyl tsobutyrate, the more powerful base sodium triphenylmethide PhaC Na leads to condensation with the formation of ethyl a-tsobutyrylisobutyrate ... [Pg.477]

Many inorganic and organic compounds possessing labile hydrogen atoms add acrylonitrile readily with the formation of compounds containing a cyancethyl grouping (—CH j. CH2. CN). This reaction is usually known as cyanoelhylation ... [Pg.914]

Asimple example is the formation of the hydrogen molecule from two hydrogen atoms. Here the original atomic energy levels are degenerate (they have equal energy), but as the two atoms approach each other, they interact to form two non degenerate molecular orbitals, the lowest of which is doubly occupied. [Pg.49]

Oxidation begins with the breakdown of hydroperoxides and the formation of free radicals. These reactive peroxy radicals initiate a chain reaction that propagates the breakdown of hydroperoxides into aldehydes (qv), ketones (qv), alcohols, and hydrocarbons (qv). These breakdown products make an oxidized product organoleptically unacceptable. Antioxidants work by donating a hydrogen atom to the reactive peroxide radical, ending the chain reaction (17). [Pg.436]

Metal Acetylides. The replacement of a hydrogen atom on acetylene by a metal atom under basic conditions results in the formation of metal acetyhdes which react with water in a highly exothermic manner to yield acetylene and the corresponding metal hydroxide. Certain metal acetyUdes can be... [Pg.373]

Hydrogen atoms can be produced in significant quantities in the gas phase by the action of radiation on or by extreme heating of H2 (3000 K). Although hydrogen atoms are very reactive, these atoms can persist in the pure state for significant periods of time because of the inabiUty to recombine without a third body to absorb the energy of bond formation. [Pg.415]

Bonding of Hydrogen to Other Atoms. The hydrogen atom can either lose the 1 valence electron when bonding to other atoms, to form the ion, or conversely, it can gain an electron in the valence shell to form the hydride ion, (see Hydrides). The formation of the ion is a very endothermic process ... [Pg.415]

Formation of Hydrogen Tetroxide. The reaction of hydrogen atoms withHquid ozone at — 196°C proceeds through the intermediate formation of hydroperoxyl radicals forming hydrogen tetroxide, which decomposes on warming to produce equimolar amounts of and O2 (53). [Pg.493]

In other cases, sulfenic acid elimination can involve y-hydrogen atoms with the formation of cyclopropane derivatives. y-Klimination is favored when DMSO is the reaction solvent. An example involving l-methylsulfinyl-2-ethyl-3-phenyl propane [14198-15-3] is shown in equation 13 (45) ... [Pg.109]

Photopolymerization reactions are widely used for printing and photoresist appHcations (55). Spectral sensitization of cationic polymerization has utilized electron transfer from heteroaromatics, ketones, or dyes to initiators like iodonium or sulfonium salts (60). However, sensitized free-radical polymerization has been the main technology of choice (55). Spectral sensitizers over the wavelength region 300—700 nm are effective. AcryUc monomer polymerization, for example, is sensitized by xanthene, thiazine, acridine, cyanine, and merocyanine dyes. The required free-radical formation via these dyes may be achieved by hydrogen atom-transfer, electron-transfer, or exciplex formation with other initiator components of the photopolymer system. [Pg.436]


See other pages where Hydrogen atom formation is mentioned: [Pg.60]    [Pg.189]    [Pg.1463]    [Pg.60]    [Pg.189]    [Pg.1463]    [Pg.146]    [Pg.713]    [Pg.436]    [Pg.102]    [Pg.141]    [Pg.143]    [Pg.324]    [Pg.49]    [Pg.123]    [Pg.90]    [Pg.335]    [Pg.114]    [Pg.62]    [Pg.266]    [Pg.490]    [Pg.266]    [Pg.288]    [Pg.220]    [Pg.495]    [Pg.454]    [Pg.443]    [Pg.431]    [Pg.47]    [Pg.95]    [Pg.117]    [Pg.224]    [Pg.565]    [Pg.403]    [Pg.325]   
See also in sourсe #XX -- [ Pg.182 ]




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