Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Oxygen addition

These are effective high-octane gasoline additive oxygenates. The conversion of isobutane into isopropyl, methyl ketone, or isopentane into isobutyl, methyl ketone is illustrative. In this reaction, no branched carboxylic acids (Koch products) are formed. [Pg.166]

When cyclohexane is nitrated to produce nitrocyclohexane [1122-60-7] the foUowiag techniques minimise undesired C—C breakage ia the ring low temperature nitrations with NO2 (31), carefiil control of the reactor temperatures, and use of halogen additives. Oxygen iacreases the level of C—C bond breakage. [Pg.36]

Oxychlorination of G2 Chlorinated Hydrocarbons. Tetrachloroethylene and trichloroethylene can be produced by reaction of EDC with chlorine or HCl and oxygen in the presence of a catalyst. When hydrochloric acid is used, additional oxygen is requked. Product distribution is varied by controlling reactant ratios. This process is advantageous in that no by-product HCl is produced, and it can be integrated with other processes as a net HCl consumer. The reactions may be represented as follows ... [Pg.28]

From the products of combustion, CO2 and 2H2O may be removed sub.sequently within the recirculation cycle before the remaining WCO2, reinforced with additional oxygen within the air supply, are fed back to the combustion chamber. Essentially, the complete combustion process described in Section 8.5.1 remains undisturbed by the carrying recirculating flue gas. [Pg.144]

A variety of oxidative reagents can be used to convert 17-hydroxypregnanes containing an additional oxygen function at C-20 into 17-ketoandrostanes. Among the most widely used have been chromium trioxide, lead tetraacetate, periodic acid and sodium bismuthate. [Pg.147]

The 17,20-glycol grouping (with or without an additional C-21 alcohol) can be cleaved to the 17-ketone by any of the four reagents. However, the presence of a 20-ketone has a marked influence on reactivity. Thus, 17a-hydroxy-20-ketones lacking additional oxygenation at C-21 are readily cleaved only by chromium trioxide. A recent report,however, claims that 17a-hydroxypregnenolone 3-acetate can be quantitatively cleaved to dehydroepiandrosterone acetate using lead tetraacetate in an aprotic solvent... [Pg.148]

Rotary kiln systems usually have a secondary combustion chamber after the kiln to ensure complete combustion of the wastes. Airtight seals close off the high end of the kiln while the lower end is connected to the secondary combustion chamber or mixing cluimber. In some cases, liquid waste is injected into the secondary combustion chamber. The kiln acts as the primary chamber to volatilize and oxidize combustibles in the wastes. Inert ash is then removed from the lower end of the kiln. The volatilized combustibles exit the kiln and enter the secondary chamber where additional oxygen is available and ignitable liquid wastes or fuel can be introduced. Complete combustion of the waste and fuel occurs in the secondar> chamber. [Pg.154]

Dipotassium phthalocyanine (PcK2) can be prepared analogously to the dilithium compound by refluxing phthalonitrile and potassium pentoxide in pentan-l-ol.58 With additional oxygen-donor ligands (e.g., crown ethers) it forms crystals with the potassium bulging outside of the phthalocyanine ring.133134... [Pg.728]

The situation is more complex, when there is an additional oxygen functionality in the a -po-sition (see Table 18)100,101. In this case the a -oxygen may also be involved in the formation of chelates, such as 28 and 29. Thus, chelation with the a -oxygen atom is expected to favor the diastereomer opposite to that from formation of an a-chelate. [Pg.80]

How does additional oxygen gets adsorbed on a fully O-covered Pt surface ... [Pg.534]

Dodecahedra of oxygen atoms at two corners and body center of unit cell, with three additional oxygen atoms (circles) needed to complete the structure. [Pg.434]

There are many similarities between the MS-MS spectra of the (M + H)" " ions of metabolites 2 and 3, with the molecnlar weight of the latter being 16 Da greater than the former. Ions occnr in both spectra at m/z 374 and 273, thns snggesting that this additional oxygen atom has been incorporated into the indan-ring part of the molecnle. [Pg.254]

Peroxy acids resemble carboxylic acids in structure, possessing just one additional oxygen atom. Peroxy acids are not very acidic, but they are used as strong oxidizing agents. Common examples of peroxy acids are ... [Pg.294]

The YSZ reactor could be operated catal3rtically or electrocatalytically, depending on the mode of oxygen addition. Oxygen could be supplied either electrochemically by means of the solid electrolyte wall of the reactor (electrocatal3 ic operation) or in the gas phase (catalsdic operation) (Fig. 1). [Pg.389]

Low-intensity light sources should give efficient irradiation of thin liquid layers [21]. Sample heating is reduced and so is radical recombination. In addition, oxygen enrichment of solutions before and after micro reactor passage can be handled differently and is no longer a major safety problem [21]. [Pg.644]

Certain requirements concerning the purity of the product to be transported must be fulfilled. For natural gas, the water content should be kept below a certain level to reduce hydrate formation. In addition, oxygen and sulfur must be controlled effectively. Some issues are presented in Table 11-1. [Pg.152]

Even sulfoxides, in which nucleophilicity is decreased by the additional oxygen, can be alkylated by methyl iodide. These sulfoxonium salts have useful synthetic applications as discussed in Section 2.5.1. [Pg.233]


See other pages where Oxygen addition is mentioned: [Pg.565]    [Pg.342]    [Pg.180]    [Pg.420]    [Pg.486]    [Pg.98]    [Pg.199]    [Pg.242]    [Pg.217]    [Pg.218]    [Pg.293]    [Pg.294]    [Pg.2223]    [Pg.2391]    [Pg.415]    [Pg.178]    [Pg.451]    [Pg.553]    [Pg.360]    [Pg.123]    [Pg.471]    [Pg.506]    [Pg.506]    [Pg.298]    [Pg.257]    [Pg.21]    [Pg.145]    [Pg.196]    [Pg.283]    [Pg.306]    [Pg.310]    [Pg.154]    [Pg.186]    [Pg.1157]   
See also in sourсe #XX -- [ Pg.646 ]




SEARCH



1,4-addition of carbon and oxygen

Addition Reactions with Formation of Carbon-Oxygen Bonds

Addition of Carbon, Oxygen, Nitrogen, and Sulfur Nucleophiles

Addition of Oxygen Nucleophiles

Addition of Oxygen and Nitrogen Nucleophiles

Addition of Radicals to Molecular Oxygen

Addition of an alkoxide and another oxygen function or a halide

Addition of carbon and oxygen nucleophiles

Addition of oxygen

Addition of oxygen atoms to double and triple bonds

Addition of oxygen to ethylenic bonds

Addition reactions oxygen terminator

Addition to Oxygen-containing Multiple Bonds

Addition to carbon-oxygen double

Addition to carbon-oxygene double bonds

Addition to carbon/oxygen double bonds

Addition to nitrogen-oxygen double bonds

Additional Oxygen Atom Transfer Reactions

Additions of Achiral and Racemic Oxygenated Allylic Stannanes to Aldehydes

Additives in slowly reacting mixtures of hydrogen and oxygen

Alkynes catalytic addition, oxygen

Asymmetric Michael additions with oxygen-based

Carbon-oxygen bonds addition

Carbon-oxygen bonds amine/alcohol addition

Carbon-oxygen bonds intermolecular additions

Carbon-oxygen bonds intramolecular additions

Carbon-oxygen bonds oxidation additions

Carbon-oxygen bonds radical additions

Carbon=oxygen double bonds, addition

Carbon=oxygen double bonds, addition reactions

Cascade Reactions Initiated by Addition of O-Centered Radicals to Alkynes (Self-Terminating Radical Oxygenations)

Cyclopentadiene, 1,4-addition oxygen

Dienols, oxygen addition

Dioxygen difluonde addition fluonne and oxygen

Electrophilic addition oxygen

Enamines oxygen addition

Fluidized with oxygen addition

Food packaging, additives oxygen scavengers

Heteroatomic coupling carbon/oxygen additions

Heteroatomic nucleophiles carbon/oxygen additions

Hydration and Other Acid-Catalyzed Additions of Oxygen Nucleophiles

Inorganic additives oxygen index effects

Intermolecular reactions oxygen nucleophile additions

Naphthalenes addition to singlet oxygen

Nitrogen-oxygen bonds double bond addition reactions

Nucleophiles oxygen, addition with

Nucleophilic Addition to the Carbon-Oxygen Double Bond

Nucleophilic addition oxygen nucleophiles

Nucleophilic addition reactions oxygen nucleophiles

Nucleophilic addition reactions with oxygen nucleophiles

Nucleophilic substitution carbon/oxygen additions

Oxidative addition model oxygen-binding

Oxidative addition oxygen nucleophiles

Oxygen addition reactions

Oxygen addition to free radicals

Oxygen addition, rate constant

Oxygen atom addition

Oxygen bases, nucleophilic addition

Oxygen nucleophiles addition reactions

Oxygen nucleophiles intermolecular additions

Oxygen nucleophiles, addition

Oxygen nucleophiles, addition regioselectivity

Oxygen nucleophiles, addition stereoselectivity

Oxygen radical addition

Oxygen selective addition

Oxygen, Beckmann rearrangement-addition

Oxygen, addition effect

Oxygen, addition effect activation

Oxygen, addition effect configuration

Oxygen, addition effect redox potential

Oxygen, addition effect reduction

Oxygen, addition effect triplet state

Oxygen, singlet addition reactions

Oxygenate additive

Oxygenate additive

Palladium complexes carbon/oxygen additions

Polar addition oxygen

Radical addition of oxygen autoxidation reactions

Silicon etching oxygen addition

Singlet oxygen addition

Singlet oxygen addition to cyclohexadiene

Singlet oxygen selective addition

© 2024 chempedia.info