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Initiated oxidation

If acetone is used there is no initial oxidation tri odo-acetone is first formed and is then converted by the sodium hydroxide to iodoform and... [Pg.92]

Manganate(VI) formed in the initial oxidation process must first be dissolved in a dilute solution of potassium hydroxide. The concentrations depend on the type of electrolytic cell employed. For example, the continuous Cams cell uses 120 150 g/L KOH and 50 60 g/L K MnO the batch-operated Bitterfeld cell starts out with KOH concentrations of 150 160 g/L KOH and 200 220 g/L K MnO. These concentration parameters minimize the disproportionation of the K MnO and control the solubiUty of the KMnO formed in the course of electrolysis. [Pg.520]

Isobutjiene [115-11-7] or tert-huty alcohol can be converted to methacrylic acid in a two-stage, gas-phase oxidation process via methacrolein as an intermediate. The alcohol and isobutjiene may be used interchangeably in the processes since tert-huty alcohol [75-65-0] readily dehydrates to yield isobutjiene under the reaction conditions in the initial oxidation. Variations of this process have been commercialized by Mitsubishi Rayon and by a joint venture of Sumitomo and Nippon Shokubai. Nippon Kayaku, Mitsui Toatsu, and others have also been active in isobutjiene oxidation research. [Pg.253]

Surface vs Solution Reactions, Anotliei issue of debate in pliotocatalyzed mineialization of oiganic substrates is whether the initial oxidation occurs on the photocatalyst s surface or in solution. Kinetic data of photooxidations and photoreductions have often been fitted to the simple... [Pg.404]

Initial production of the dimethyl terephthalate started with the oxidation of -xylene to terephthaUc acid using nitric acid both companies reportedly used similar technology (43—45). Versions of the nitric acid oxidation process, which has been abandoned commercially, involved the use of air in the initial oxidation step to reduce the consumption of nitric acid (44,46,47). The terephthaUc acid was then esterified with methanol to produce dimethyl terephthalate, which could be purified by distillation to the necessary degree (48). [Pg.487]

The effect substitution on the phenolic ring has on activity has been the subject of several studies (11—13). Hindering the phenolic hydroxyl group with at least one bulky alkyl group ia the ortho position appears necessary for high antioxidant activity. Neatly all commercial antioxidants are hindered ia this manner. Steric hindrance decreases the ability of a phenoxyl radical to abstract a hydrogen atom from the substrate and thus produces an alkyl radical (14) capable of initiating oxidation (eq. 18). [Pg.224]

Dehalogenation of monochlorotoluenes can be readily effected with hydrogen and noble metal catalysts (34). Conversion of -chlorotoluene to Ncyanotoluene is accompHshed by reaction with tetraethyl ammonium cyanide and zero-valent Group (VIII) metal complexes, such as those of nickel or palladium (35). The reaction proceeds by initial oxidative addition of the aryl haHde to the zerovalent metal complex, followed by attack of cyanide ion on the metal and reductive elimination of the aryl cyanide. Methylstyrene is prepared from -chlorotoluene by a vinylation reaction using ethylene as the reagent and a catalyst derived from zinc, a triarylphosphine, and a nickel salt (36). [Pg.53]

Alkylaziridines can be stereospecifically deaminated to alkenes by reaction with m-chioroperbenzoic acid (70AG(E)374). The reaction and work-up are carried out in the dark to avoid isomerization of the cw-alkene, and the mechanism is thought to involve an initial oxidation to an amine oxide followed by a concerted elimination. Aziridine oxides have been generated by treating aziridines with ozone at low temperatures (71JA4082). Two... [Pg.74]

Manganese, copper, iron, cobalt and nickel ions can all initiate oxidation. Untinned copper wire can have a catastrophic effect on natural rubber compounds with which it comes into contact. Inert fillers for use in rubbers are usually tested for traces of such metal ions, particularly copper and manganese. The problem is perhaps less serious in saturated hydrocarbon polymers but still exists. [Pg.140]

Nicolaou and co-workers established the severely strained A-ring oxazole (21) in their total synthesis of antitumor agent diazonamide A through initial oxidation of the hindered alcohol of intermediate 20 with TPAP and subsequent Robinson-Gabriel cyclodehydration of the resultant ketoamide with a mixture of POCI3 and pyridine (1 2) at 70°C. ... [Pg.252]

The stoichiometry of the prepared compounds depends not only on the composition of the initial mixture, but also on the initial oxide s fluorination activity. Unlike tantalum oxide, fluorination of niobium oxide by an ammonium hydrofluoride melt results in the formation of oxyfluoroniobates, but not of fluoroniobates. During the first step of Nb205 fluorination, (NH4)3NbOF6 is formed according to the following interaction [51, 52, 105, 111, 121, 122] ... [Pg.49]

In other cases, if the fluorination process leads to cardinal changes in the crystal structure of the initial oxide compounds, new compounds with polar structures can be obtained. A demonstrative example of such materials are compounds that belongs to the system Na5(W3 xNbx)09..xF5+x and that have chiolite-type structures, when neither pure fluoride nor oxide display any ferroelectric properties [393 - 395]. [Pg.218]

The intramolecular Heck reaction presented in Scheme 8 is also interesting and worthy of comment. Rawal s potentially general strategy for the stereocontrolled synthesis of the Strychnos alkaloids is predicated on the palladium-mediated intramolecular Heck reaction. In a concise synthesis of ( )-dehydrotubifoline [( )-40],22 Rawal et al. accomplished the conversion of compound 36 to the natural product under the conditions of Jeffery.23 In this ring-forming reaction, the a-alkenylpalladium(n) complex formed in the initial oxidative addition step engages the proximate cyclohexene double bond in a Heck cyclization, affording enamine 39 after syn /2-hydride elimination. The latter substance is a participant in a tautomeric equilibrium with imine ( )-40, which happens to be shifted substantially in favor of ( )-40. [Pg.574]

GPI Glass Packaging Institute IOT initial oxidation temperature... [Pg.651]

This minor but important route enables a quinoxalinamine to be converted into the corresponding nitroquinoxaline by oxidation of a derived dimethylsulfimido-quinoxaline. Thus 3-chloro-2-quinoxalinamme (24) was converted into 2-chloro-3-dimethylsulfimidoquinoxahne (25) (68-88% see Section 6.3.2.4), which underwent initial oxidation to a green solution of 2-chloro-3-nitrosoquinoxaline (26) (m-ClC6H4C03H, CH2CI2, 5°C, 40 min then Me2SJ 0°C, 10 min) and thence further oxidation to 2-chloro-3-nitroquinoxaline (27) (O3J, 0°C, until colorless 20-... [Pg.260]

Certain electrode reactions occur by a mechanism which involves initial oxidation or reduction of one of the components of the electrolysis medium. This species is commonly reformed later in the reaction se-... [Pg.176]

Primary alcohols can be selectively detected using reagent sequences involving an initial oxidation to yield aldehydes that are then reacted in acid medium with electron-rich aromatics or heteroaromatics, according to the above scheme, to yield intensely colored triphenylmethane dyes. [Pg.39]

Phenols are probably initially oxidized to quinones, which then presumably react further to yield triphenylmethane dyestuffs. [Pg.108]

Peroxide decomposers—These function by reacting with the initiating peroxides to form nonradical products. Presumably mercaptans, thiophenols, and other organic sulfin compounds function in this way [19]. It has been suggested that zinc dialkyldithiocarbamates function as peroxide decomposers, thus giving mbber compounds good initial oxidative stability. [Pg.467]

Physical properties of carbon black-filled EPR and EPDM elastomers have been found to be comparable with the suUur-cured analogues [372]. Aromatic oils increase the optimum dose requirement for these compounds due to the reaction of the transient intermediates formed during radiolysis of the polymer with the oil as well as energy transfer which is particularly effective when the oil contains aromatic groups. The performance and oxidative stability of unfilled EPDM as well as its blend with PE [373], and the thermal stabdity and radiation-initiated oxidation of EPR compounds are reported by a number of workers [374,375]. [Pg.882]


See other pages where Initiated oxidation is mentioned: [Pg.2398]    [Pg.92]    [Pg.25]    [Pg.522]    [Pg.479]    [Pg.525]    [Pg.36]    [Pg.290]    [Pg.13]    [Pg.23]    [Pg.196]    [Pg.255]    [Pg.256]    [Pg.131]    [Pg.964]    [Pg.113]    [Pg.72]    [Pg.17]    [Pg.270]    [Pg.704]    [Pg.388]    [Pg.9]    [Pg.569]    [Pg.222]    [Pg.335]    [Pg.336]    [Pg.339]    [Pg.830]    [Pg.117]    [Pg.50]    [Pg.467]   


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AIBN-initiated oxidation

AIBN-initiated oxidation cumene

Chain initiation, oxidation

Cholesterol oxidation, initiation

Domino Reactions Initiated by Oxidation or Reduction

Domino Reactions Initiated by an Oxidation Reaction

Ethylene oxide lithium-based initiators

Free radical lipid oxidation initiation

Free radical oxidation, ultraviolet light initiates

Heme proteins lipid oxidation initiation

Initial oxidation temperature

Initiated oxidation 2-methylpropane

Initiation lipid oxidation

Initiation of oxidation

Initiation oxidation chemistry

Initiation polymer oxidation

Initiation reaction propylene oxide addition

Initiation step photo-oxidative degradation

Initiation, oxidation

Initiators transition metal oxides

Metal Oxide Initiation

OH-initiated oxidation

Oxidation enzyme-initiated

Oxidation initial, thin film

Oxidation processes initiation

Oxidation, initiation/spreading, imaging

Oxidation/reduction initiated domino

Oxidative activation initial step

Oxidative damage initiated inflammation

Photo-initiated oxidation

Photo-initiated oxidation, treatment

Photo-initiated oxidation, treatment structure of intermediary products

Proteins redox oxidation initiated

Reactions Initiated by Oxidation or Reduction

Reduction-oxidation initiation

Silver oxide initiator

Xenobiotics, initial oxidation

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