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Atoms oxidation

Polybutadiene and polyunsaturated fats, which contain aHyUc hydrogen atoms, oxidize more readily than polypropylene, which contains tertiary hydrogen atoms. A linear hydrocarbon such as polyethylene, which has secondary hydrogens, is the most stable of these substrates. [Pg.223]

Chlorinated organics are hydrocarbons that have one or many chlorine atoms. Oxidation of chlorinated hydrocarbons yields COj, water vapor and hydrogen chloride (HCl) gas. Some typical chlorinated organics are TCE and PCE. These organics have calorific values as low as 5,000 BTU/lb. [Pg.479]

In reaction (76) the oxidation number of sulfur changes from +4 to 4-6. According to this, two electrons are released by each sulfur atom oxidized. Show that these electrons are gained by oxygen if we assume oxygen has oxidation number equal to zero in O2. [Pg.217]

Figure 18-10 summarizes the successive oxidation products that can be obtained from alcohols. When the hydroxyl group, OH, is attached on an end carbon atom, an aldehyde and a carboxylic acid can be obtained through oxidation. When the hydroxyl group is on a carbon atom attached to two other carbon atoms, oxidation gives a ketone. Huge amounts of aldehydes and ketones are used industrially in a variety of chemical processes. Furthermore, these functional groups are important in chemical syntheses of medicines, dyes, plastics, and fabrics. [Pg.335]

Figure 2.9 Schematic structures of Fe-S redox centres, their electron-transfer reactions and approximate range of potentials. See text for details. Individual iron atom oxidation states are not specified for delocalized cluster spin states are indicated. Reprinted with permission from Holm et al., 1996. Copyright (1996) American Chemical Society. Figure 2.9 Schematic structures of Fe-S redox centres, their electron-transfer reactions and approximate range of potentials. See text for details. Individual iron atom oxidation states are not specified for delocalized cluster spin states are indicated. Reprinted with permission from Holm et al., 1996. Copyright (1996) American Chemical Society.
Whereas, in imidates, an O-atom is attached to the sp2 C-atom, in another class of imines, the amidines, a N-atom is attached to the sp2 C-atom. Oxidative cleavage of benzamidines has been discussed (Chapt. 5 in [50]). Here, we present studies in which formamidines were examined (N-CH=N-R) as potential prodrugs of anti-HIV cytidine analogues [103]. Specifically, the... [Pg.713]

As shown in Fig. 14.24, a self-regulating oxidizer feeding mechanism is used to eliminate the liquid oxidizer pumping system. A flow of the pressurized fuel-rich gas generated in tlie primary combustor forces the oxidizer tank to supply the liquid oxidizer to the secondary combustor. Simultaneously, the fuel-rich gas is injected into the secondary combustor and reacts with the atomized oxidizer. The fuel-rich gas is injected from the primary combustor into the secondary combustor through the fuel gas injector under condihons of a choked gas flow. The pressure in the primary combustor is approximately double that in the secondary combustor. This system is termed a gas-pressurized system. [Pg.431]

Though the pyrolants used in gas-hybrid rockets burn in a similar manner as rocket propellants, their chemical compositions are fuel-rich. The pyrolants burn incompletely and the combustion temperature is below about 1000 K. When an atomized oxidizer is mixed with the fuel-rich gas in the secondary combustor, the mixture reacts to generate high-temperature combustion products. The combushon performance designated by specific impulse, is dependent on the combinahon of pyrolant and oxidizer. [Pg.433]

Diester 352 (Scheme 74, Section 4.2 (1994SC2685)) after the sulfur atom oxidation undergoes hydrolysis and intramolecular acylation to the pyrrolo-thiadiazepine 353 with a fused lactam ring. [Pg.63]

A case of a pentavalent phosphorus-atom oxidation is documented for a.a-dicarbonyl-phosphoranes (equation 17)". When treated with DMD, the corresponding a tricarbonyl... [Pg.1154]

As already seen, the reactions of OH, N03, and Cl with alkanes generate alkyl radicals. We shall see in the subsequent sections of this chapter that the production of alkyl radicals of various types is a general characteristic of organic oxidations. Here we will trace the atmospheric fates of typical alkyl radicals formed in OH, NO-, and Cl atom oxidations of alkanes. However, the principles are general and can be applied to those formed by the reactions of other organics such as alkenes as well. [Pg.185]

Oxidation Aliphatic Carbon Atoms. Oxidation at the terminal carbon atom of an alkyl substituent is co-oxidation oxidation of the carbon atom located second from the end is co-1 oxidation. Unless specifically catalyzed by an enzyme, co-1 oxidation tends to occur more frequently. The anticonvulsant drug ethosuximide is metabolized at both the CO and co-1 position. [Pg.147]

A chemical equation for the combustion of propane, C3H8, is shown in exercise 67. Through this reaction are the oxygen atoms oxidized or reduced ... [Pg.385]

Neutroi atom Oxidation state Neutral atom ... [Pg.325]

This section contains considerable material on the proper writing of Formulae, much of it routine, some of it highly specialized. Most of the indicators of the number of atoms, oxidation state, ionic charge, optical activity, and structures are very similar to those for names and will be discussed in later sections, especially Section 1-10.]... [Pg.519]

Fluoroalkyl iodides are oxidized at the iodine atom by trifluoroperacetic acid3 7- 19 or by a mixture of trifluoroacetic anhydride with hydrogen peroxide the products are [bis(trifluoro-acetoxy)iodo]fluoroalkanes, e.g. oxidation of 1 to 2. The iodine atom oxidized in the reactions can be attached either to a nonfluorinated317 318 or a fluorinated carbon atom.319... [Pg.79]


See other pages where Atoms oxidation is mentioned: [Pg.218]    [Pg.18]    [Pg.278]    [Pg.603]    [Pg.263]    [Pg.318]    [Pg.269]    [Pg.99]    [Pg.556]    [Pg.241]    [Pg.495]    [Pg.401]    [Pg.197]    [Pg.27]    [Pg.202]    [Pg.431]    [Pg.275]    [Pg.16]    [Pg.601]    [Pg.1235]    [Pg.431]    [Pg.472]    [Pg.40]    [Pg.424]    [Pg.326]    [Pg.853]    [Pg.288]    [Pg.278]    [Pg.259]    [Pg.18]    [Pg.94]   
See also in sourсe #XX -- [ Pg.11 ]




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Actinides oxidation states, 442 --- atomic properties

Adsorption of atomic, molecular, and cluster particles on metal oxides

Amide oxides reactions with transition metal atoms

Atom transfer, oxidative addition

Atom-economic oxidation

Atomic Layer Deposition of Metal oxides

Atomic Oxygen Activation Alcohol Electro-Oxidation

Atomic layer deposition metal oxides

Atomic resolution ETEM of butane oxidation

Atomization dimeric oxides

Carbon atoms oxidation states

Carbonyl oxides oxygen atom transfer

Central atom concepts oxidation states

Central atom, oxidation state

Chromium atom formal oxidation states

Cobalt atom formal oxidation states

Hydrogen atom transfer enzymatic oxidation

Hydrogen atoms, oxidation number

Magnesium oxide, atomic carbon

Mechanisms oxidation-reduction, hydrogen atom transfer

Metal atoms nitric oxide

Metal atoms oxidation reactions

Metal atoms reaction with cyclohexene oxide

Nitric oxide reaction with atomic

Nitric oxide, reaction + metal atoms

Nitrogen oxide clusters atomic oxygen

Nitrous oxide metal atoms

Nitrous oxide, reaction + metal atoms

Oxidation Numbers of Atoms

Oxidation at the Thiophene Sulfur Atom

Oxidation at the sulfur atom

Oxidation atomic oxygen

Oxidation by Chlorine Atoms

Oxidation by Hydroxyl Radical and hydrogen atoms

Oxidation by Oxygen Atom Transfer

Oxidation by atomic oxygen

Oxidation carbon atom

Oxidation combined halogen atom

Oxidation of Non-functional Carbon Atoms

Oxidation of Sulfur Atoms the MacDonald-Fischer Degradation

Oxidation of hydrocarbons containing four carbon atoms

Oxidation or reduction of central atoms

Oxidation state, atoms

Oxidation state, of atoms in a molecule

Oxidation sulfur atom

Oxidation with oxygen atoms

Oxidations at Unfunctionalized Carbon Atoms

Oxidative Additions to Metal Atoms and Slurries

Oxidative Degradation of 1 C Atom (Hexose-pentose Transition)

Oxidative addition atom abstraction

Oxidative addition, metal atom-organic

Oxidative addition, metal atom-organic complexes

Oxide films atomic layer deposition

Oxygen atom transfer saturated hydrocarbon oxidation

Oxygen atoms oxidation states

Oxygen atoms, oxidation number

Replacement, benzenesulfonate groups oxide oxygen atom by sulfur

Single Atoms on Oxide Surfaces

Surface atom oxidation

Transition metal atoms formal oxidation states

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