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C-0 oxidation

Borneol and isoboineol are respectively the endo and exo forms of the alcohol. Borneol can be prepared by reduction of camphor inactive borneol is also obtained by the acid hydration of pinene or camphene. Borneol has a smell like camphor. The m.p. of the optically active forms is 208-5 C but the racemic form has m.p. 210-5 C. Oxidized to camphor, dehydrated to camphene. [Pg.64]

CHjCOCOOH. A colourless liquid with an odour resembling that of ethanoic acid, m.p. 13 C, b.p. 65 C/lOmm. It is an intermediate in the breakdown of sugars to alcohol by yeast. Prepared by distilling tartaric acid with potassium hydrogen sulphate. Tends 10 polymerize to a solid (m.p. 92 C). Oxidized to oxalic acid or ethanoic acid. Reduced to ( + )-Iactic acid. [Pg.336]

Fig. 2. Overall schematic of solid fuel combustion (1). Reaction sequence is A, heating and drying B, solid particle pyrolysis C, oxidation and D, post-combustion. In the oxidation sequence, left and center comprise the gas-phase region, tight is the gas—solids region. Noncondensible volatiles include CO, CO2, CH4, NH, H2O condensible volatiles are C-6—C-20 compounds oxidation products are CO2, H2O, O2, N2, NO, gaseous organic compounds are CO, hydrocarbons, and polyaromatic hydrocarbons (PAHs) and particulates are inerts, condensation products, and solid carbon products. Fig. 2. Overall schematic of solid fuel combustion (1). Reaction sequence is A, heating and drying B, solid particle pyrolysis C, oxidation and D, post-combustion. In the oxidation sequence, left and center comprise the gas-phase region, tight is the gas—solids region. Noncondensible volatiles include CO, CO2, CH4, NH, H2O condensible volatiles are C-6—C-20 compounds oxidation products are CO2, H2O, O2, N2, NO, gaseous organic compounds are CO, hydrocarbons, and polyaromatic hydrocarbons (PAHs) and particulates are inerts, condensation products, and solid carbon products.
Fig. 7. NO formation for the Provo-Orem bus mn at a compression ratio of 12 1 at 30°C, 3000 rpm, where A is brake mean effective pressure B, brake thermal efficiency and C, oxides of nitrogen, (a) Effect of equivalence ratio, ( ), at a water/H2 mass ratio of 6.0 and spark = 17° before top-dead (BTC) and (b), effect of water injection where (j) = 0.60 and spark = 14°BTC. To convert MPa to psi, multiply by 14. Fig. 7. NO formation for the Provo-Orem bus mn at a compression ratio of 12 1 at 30°C, 3000 rpm, where A is brake mean effective pressure B, brake thermal efficiency and C, oxides of nitrogen, (a) Effect of equivalence ratio, ( ), at a water/H2 mass ratio of 6.0 and spark = 17° before top-dead (BTC) and (b), effect of water injection where (j) = 0.60 and spark = 14°BTC. To convert MPa to psi, multiply by 14.
The continuous softening process used by The Broken Hill Associated Smelters Pty., Ltd. is particularly suitable for lead buUion of fairly uniform impurity content. The copper-drossed blast furnace buUion continuously flows in the feed end of a reverberatory furnace at 420°C, and the softened lead leaves the opposite end at 750°C. Oxidation and agitation is provided by compressed air blown through pipes extending down through the arch of the furnace into the bath. [Pg.44]

The aromatic rings of kraft lignins can be sulfonated to varying degrees with sodium sulfite at high temperatures (150—200°C) or sulfomethylated with formaldehyde and sulfite at low temperatures (<100° C). Oxidative sulfonation with oxygen and sulfite is also possible. [Pg.145]

Variety and source Si02 (siHca ) FeO (ferrou s oxide) 3 (ferri c oxide ) AI2O3 (alumina) MgO (magnesia) CaO (lime ) MnO (manganese oxide) Na20 (sodiu m oxide) icp (potassiu m oxide) up, adsoibe d up+, combine d... [Pg.346]

At ambient temperatures beryUium is quite resistant to oxidation highly poHshed surfaces retain the brilliance for years. At 700°C oxidation becomes noticeable in the form of interference films, but is slow enough to permit the working of bare beryUium in air at 780°C. Above 850°C oxidation is rapid to a loosely adherent white oxide. The oxidation rate at 700°C is paraboHc but may become linear at this temperature after 24—48 hours of exposure. In the presence of moisture this breakaway oxidation occurs more rapidly and more extensively. BeryUium oxide [1304-56-9] BeO, forms rather than beryUium nitride [1304-54-7] Be2N2, but in the absence of oxygen, nitrogen attacks beryUium above 900°C. [Pg.66]

RL Cutler, AM Davies, S Creighton, A Warshel, GR Moore, M Smith, AG Mauk. Role of arginine-38 in regulation of the cytochrome c oxidation-reduction equilibrium. Biochemistry 28 3188-3197, 1989. [Pg.414]

FIGURE 21.9 Typical visible absorption spectra of cytochromes, (a) Cytochrome c, reduced spectrum (b) cytochrome c, oxidized spectrum (c) the difference spectrum (a) minus (b) (d) beef heart mitochondrial particles room temperature difference (reduced minus oxidized) spectrum (e) beef heart submitochondrial particles same as (d) but at 77 K. a- and /3- bauds are labeled, and in (d) and (e) the bauds for cytochromes a, h and c are indicated. [Pg.685]

Based oil 11PLC analysis using a chiral column (Waters OptiPak TC). h Yield after purification by column chromatography. c Oxidative removal of the 2-isopropyl-4-methoxyphenyl moiety from 3 is unsuccessful. [Pg.694]

Ferrocyanides stability, 6, 830 Ferrocytochrome c oxidation, 6, 621 Ferroin, 4,1203 redox indicator. 1,558 Ferrokinetics... [Pg.129]


See other pages where C-0 oxidation is mentioned: [Pg.30]    [Pg.57]    [Pg.123]    [Pg.279]    [Pg.429]    [Pg.395]    [Pg.225]    [Pg.748]    [Pg.266]    [Pg.512]    [Pg.58]    [Pg.242]    [Pg.73]    [Pg.85]    [Pg.88]    [Pg.173]    [Pg.748]    [Pg.707]    [Pg.717]    [Pg.285]    [Pg.299]    [Pg.902]    [Pg.842]    [Pg.918]    [Pg.997]    [Pg.1089]    [Pg.659]    [Pg.95]    [Pg.229]    [Pg.228]    [Pg.229]    [Pg.414]    [Pg.969]    [Pg.990]    [Pg.22]    [Pg.983]    [Pg.983]    [Pg.1005]    [Pg.1006]   
See also in sourсe #XX -- [ Pg.298 ]




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Allylic C-H bonds oxidation

Allylic C-H oxidation

Butane. Oxidation at secondary and primary C—H bonds

C alcohol oxidation

C oxidative

C oxidative cyclizations

C-CN Bond Cleavage via Oxidative Addition

C-H Oxidation Tsutomu Katsuki

C-H bond oxidative addition

C-H oxidative addition

C-O oxidation

C-O oxidative addition

C-X-Y-Fragment (Nitrile Oxide on Solid Phase)

C-rare earth oxide

C/S-CYCLOOCTENE OXIDE

CS Modified with Zinc, Titanium, and Zirconium Oxides

Chiral allylic C-H oxidation

Cytochrome c oxidized

C—H bonds, oxidation

C—H oxidation

Early History of C-H Bond Oxidative Addition

Intermolecular C-H oxidation

Intramolecular C-H oxidation

Microbial Oxidation of Non-activated C-H Bond

Microbial oxidation unactivated C—H bonds

Organometallic Complexes as Catalysts in Oxidation of C—H Compounds

Oxidation C-H bond activation

Oxidation activated C—H bonds

Oxidation and nitration of C-N bonds

Oxidation at C(l)

Oxidation by C-H Bond Cleavage

Oxidation of Benzylic C-H Bonds

Oxidation of C-H Bonds in Alkanes

Oxidation of C-H bonds

Oxidation of CS

Oxidation of Saturated Unactivated and Activated C-H Bonds

Oxidation of the C-H bond in acetals

Oxidation unactivated C—H bonds

Oxidations of C-N bonds

Oxidative Addition and C — H Bond Activation

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

Oxidative addition of C-H bond

Oxidative addition of alkane C-H bonds

Oxidative addition of the formyl C-H bond

Oxidative addition of the ortho C-H bond

P-C Heterocycles (Dibenzophosphole Oxides)

Properties of Pyrazine A-Oxides and their C-Alkyl Derivatives

Reaction C.—Oxidation of the Side Chain in Aromatic Compounds

Soot oxidation (C. R. Shaddix)

Supersaturation leading to a modified mechanism for the formation of CS planes in oxides

Trimethylamine N-oxide C—Si bonds

Type C oxides

Wacker oxidation C—O bond formation

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