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ARBON

Before we start with a systematic discussion of the syntheses of difunctional molecules, we have to point out a formal difficulty. A carbonmultiple bond is, of course, considered as one functional group. With these groups, however, it is not clear, which of the two carbon atoms has to be named as the functional one. A 1,3-diene, for example, could be considered as a 1,2-, 1,3-, or 1,4-difunctional compound. An a, -unsaturated ketone has a 1.2- as well as a 1,3-difunctional structure. We adhere to useful, although arbitrary conventions. Dienes and polyenes are separated out as a special case. a, -Unsaturated alcohols, ketones, etc. are considered as 1,3-difunctional. We call a carbon compound 1,2-difunctional only, if two neighbouring carbon atoms bear hetero atoms. [Pg.50]

Figure B-19. Propane pressure-enthalpy diagram. (From Edmister and Lee, Apftfifd IfyJrot arbon Thermodynamics, Voi. I. Second Edition, Gulf Publishing Company, Houston, TX, 1984.)... Figure B-19. Propane pressure-enthalpy diagram. (From Edmister and Lee, Apftfifd IfyJrot arbon Thermodynamics, Voi. I. Second Edition, Gulf Publishing Company, Houston, TX, 1984.)...
Based upon C arbon Steel Rings other weights are Stainless Steel 105% Copper 120% Aluminum 37% Monel and Nickel 115%. [Pg.249]

In a 1-1. round-bottomed flask equipped with a condenser are placed 78.0 g. (0.56 mole) of commercial anhydrous potassium arbonate, 45.0 g. (0.50 mole) of methallyl chloride (Note 1), 55.0 g. (0.55 mole) of 2,4-pentanedione (Note 1), and 300 ml. of anhydrous ethanol (Note 2). The mixture is refluxed on a steam bath for 16 hours. The condenser is replaced by a distilling head and condenser, and about 200 ml. of ethanol is distilled from the mixture (Note 3). Ice water (600 ml.) is added to dissolve the salts, and the mixture is extracted three times with ether. The... [Pg.87]

FIGURE 14.42 A typical silicone structure. The hydroc arbon groups give the substance a water-repelling quality. Note the similarity of this structure to that of the purely inorganic pyroxenes in Fig. 14.38. [Pg.734]

Rcl crcnce method Hydr[Pg.230]

Spangenberg, J. E., Jacomet, J. and Schibler, J. (2006) Chemical analyses of organic residues in archaeological pottery from Arbon Bleiche 3, Switzerland evidence for dairying in the late Neolithic. Journal of Archaeological Science 33, 1 13. [Pg.431]

Luellen, D.R. and Shea, D. 2002, Calibration and field verification of semipermeable membrane devices for measuring polycyclic aromatic hydrrx arbons in water Environ. Sci. Technol. 36 1791-1797. [Pg.201]

C arbon amxie Carbon cathode Dhri d cell... [Pg.59]

The carbon-bond-forming reactions based on hydrogen transfer catalyzed by Cp Ir complex have been extended to the alkylation of active methylene compounds. Grigg et al. reported the alkylation of arylacetonitriles catalyzed by the... [Pg.131]

Reaction of linear conjugated dienes with la at —10 °C in hydrocarbon solvent in the presence of McsSiCl/AlCls affords stereospecific tra i-l-silyl-3-vinyl-cyclopentanes, indicating a [3 + 2] cycloaddition of the allyl group of la with a carbon arbon double bond of the diene [Eq. (9)]. In the [3 + 2] annulation reaction, of greater significance is the tram conformation of the trimethylsilyl group and vinyl groups. [Pg.46]

The feed gas flow rate was monitored and controlled by mass flow controllers. Product gases were fed through heated stainless steel lines to a sample loop in an automated gas chromatograph. The GC analysis was performed using two isothermal columns (80°C) in series, a Porapak T and a Molecular Sieve 5A column. When necessary, a second GC analysis using a temperature programmed Hayesep R column was used to separate and detect small hydnx arbons (such as ethylene and ethane) and H2O. [Pg.418]

The capacity for benzo[a]pyiene metabolism (viz. aryl hydrcx arbon hydroxylase activity) in fish and shellfish can be used as a measure of the induction of this enzyme by environmental polycyc c hydrocarbon pollutants and has been suggested (Mix and Schaffer, 1979 Kuidec et... [Pg.32]


See other pages where ARBON is mentioned: [Pg.345]    [Pg.116]    [Pg.48]    [Pg.11]    [Pg.2]    [Pg.401]    [Pg.1207]    [Pg.209]    [Pg.233]    [Pg.44]    [Pg.49]    [Pg.504]    [Pg.102]    [Pg.399]    [Pg.767]    [Pg.20]    [Pg.40]    [Pg.84]    [Pg.627]    [Pg.174]    [Pg.210]    [Pg.1]    [Pg.199]    [Pg.110]    [Pg.27]    [Pg.244]    [Pg.70]    [Pg.539]    [Pg.555]    [Pg.559]    [Pg.40]    [Pg.943]    [Pg.1102]    [Pg.324]    [Pg.232]    [Pg.321]   


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ARBON BLACK

ARBON DIOXIDE

ARBON MONOXIDE

Carbon bonds arbon-nitrogen

Korovin arbon Anodes for Lithium-Ion Batteries

M. Galinski arbon Materials for Gas Diffusion Electrodes, Metal Air ells and Batteries

Ralph C. Bick and Sirichai Panichanum arbon-13 NMR Spectroscopy of Steroidal Alkaloids

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