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Substance compounds

Compound A undergoes hydrolysis of its acetal function in dilute sulfuric acid to yield 1,2-ethanediol and compound B (CgHg02), mp 54°C. Compound B exhibits a carbonyl stretching band in the infrared at 1690 cm and has two singlets in its H NMR spectrum, at 8 2.9 and 6.7, in the ratio 2 1. On standing in water or ethanol, compound B is converted cleanly to an isomeric substance, compound C, mp 172—173°C. Compound C has no peaks attributable to carbonyl groups in its infrared spectrum. Identify compounds B and C. [Pg.1023]

Korper, m. body substance, compound Elec.) earth, ground. (Careful modern usage avoids the translation body for chemical substances.)... [Pg.257]

Substance (compound it most resembles) vap experimental Pvap estimated... [Pg.40]

Substance Compound Boiling Point at Atmospheric Pressure (°C) Henry s Law Constant, Ha [atm (Mole Fraction ) 1]... [Pg.69]

Enthalpies of reaction can also be calculated from individual enthalpies of formation (or heats of formation), AHf, for the reactants and products. Because the temperature, pressure, and state of the substance will cause these enthalpies to vary, it is common to use a standard state convention. For gases, the standard state is 1 atm pressure. For a substance in an aqueous solution, the standard state is 1 molar concentration. And for a pure substance (compound or element), the standard state is the most stable form at 1 atm pressure and 25°C. A degree symbol to the right of the H indicates a standard state, AH°. The standard enthalpy of formation of a substance (AHf) is the change in enthalpy when 1 mol of the substance is formed from its elements when all substances are in their standard states. These values are then tabulated and can be used in determining A//°rxn. [Pg.127]

Nonhumic substances Compounds belonging to known classes of biochemistry, such as amino acids, carbohydrates, fats, waxes, resins, and organic acids. Humus probably contains most, if not all, of the biochemical compounds synthesized by living organisms... [Pg.14]

At the time of the discovery of radio-activity, about seventy-five substances were called elements in other words, about seventy-five different substances were known to chemists, none of which had been separated into unlike parts, none of which had been made by the coalescence of unlike substances. Compounds of only two of these substances, uranium and thorium, are radio-active. Radio-activity is a very remarkable phenomenon. So far as we know at present, radio-activity is not a property of the substances which form almost the whole of the rocks, the waters, and the atmosphere of the earth it is not a property of the materials which constitute living organisms. It is a property of some thirty substances—of course, the number may be increased—a few of which are found widely distributed in rocks and waters, but none of which is found anywhere except in extraordinarily minute quantity. Radium is the most abundant of these substances but only a very few grains of radium chloride can be obtained from a couple of tons of pitchblende. [Pg.87]

Naturally occurring substances compounds leached from the earths crust (calcium, heavy metals) and leachates from soils and sediments (humic and fulvic acids). [Pg.714]

Fig. 10.25. Separation of tipredane (compound 14) from its five related substances (compounds 11-13, 15, 16) by CEC. Column 250 mm x 50 pm i.d. packed with 3 pm Spherisorb ODS-1 mobile phase, acetonitrile-50 mM Tris buffer, pH 7.8, 80 20 (v/v) applied voltage, 15 kV temperature, 15°C electrokinetic injection, 5 kV/15s. From Euerby et al. [63], Journal of Microcolumn Separations, 1997. Reproduced with permission of John Wiley Sons, Inc. Fig. 10.25. Separation of tipredane (compound 14) from its five related substances (compounds 11-13, 15, 16) by CEC. Column 250 mm x 50 pm i.d. packed with 3 pm Spherisorb ODS-1 mobile phase, acetonitrile-50 mM Tris buffer, pH 7.8, 80 20 (v/v) applied voltage, 15 kV temperature, 15°C electrokinetic injection, 5 kV/15s. From Euerby et al. [63], Journal of Microcolumn Separations, 1997. Reproduced with permission of John Wiley Sons, Inc.
Warning. Many of the nitrogen-fluorine compounds discussed in this section are very hazardous materials. Their syntheses should not be undertaken without adequate shielding equipment and a prior knowledge of techniques for the handling of explosive substances. Compounds of this type are labeled extra-hazardous or hazardous, depending upon properties of the material. [Pg.299]

Nonselective attacks at the carbon combined with a nitro group and carbon combined with the N(O) atom of the azoxy group were observed in the reaction of 4,4 -dinitroazoxyfurazan with bases and nucleophiles [468], The preparation of dinitro polyfurazans shows the great synthetic potential of the construction sequence. The simplicity and availability of the starting substances (compounds) makes this strategy a powerful method for high energetic material construction. [Pg.40]

Paraffins.—Carbon and hydrogen do not unite directly under ordinary laboratory conditions but in certain natural substances compounds of the two elements are present. Similar compounds of the two elements may also be formed by the decomposition of complex substances containing other elements than carbon and hydrogen. The hydrocarbons so found or formed are usually very stable compounds and... [Pg.3]

Take a moment to recall what you have learned about the organization of matter, using Figure 3-17 as a guide. You know that matter is classified as pure substances and mixtures. As you learned in the previous section, mixtures can be homogeneous or heterogeneous. You also know that elements are pure substances that cannot be separated into simpler substances. There is yet another classification of pure substances—compounds. A compound is a combination of two or more different elements that are combined chemically. Most of the substances that you are familiar with and, in fact, much of the matter of the universe are compounds. Water, table salt, table sugar, and aspirin are examples of common compounds. [Pg.71]

As an approach to investigating the complex chemistry of natural foams, humic substances (compounds sufficiently nonpolar at pH 2.0 to be isolated by reverse phase on XAD-8 and recovered in 0.1 N sodium hydroxide) were isolated from aquatic foam and associated stream water for chemical characterization and investigations into surfactant behavior. Humic substances were chosen because they represent natural organic compounds present in natural waters that are sufficiently nonpolar at pH 2.0 to be isolated by XAD-8 adsorption. As surfactants also possess moderately nonpolar characteristics it follows that humic substances may contain a significant surfactant component. We hypothesized that foam would be enriched in humic substances compared to stream samples and would show increased hydrophobicity, aliphaticity, and decreased carboxylation in order to sustain surface-active behavior. [Pg.152]

The preponderance of analytical (and preparative) separations that precede mass spectrometric analyses are carried out using HPLC. Despite its potential for extremely high efficiencies, capillary electrophoresis (CE) remains something of a specialized application, particularly with mass spectrometric detection. The technique is hampered by its reliance on small sample volumes (typically nL injections) in order to avoid loss of separation efficiency. The consequence of these small volumes is a concentration detection limit that is substantially higher than that of techniques such as HPLC. Despite the exquisite sensitivity of mass spectrometers, characterization of related substances present at low femtomole levels (assuming a hypothetical related substance compound with molecular weight 500 daltons present at 0.1% w/w in an equally hypothetical drug substance sample... [Pg.262]

Recognize various forms of matter homogeneous and heterogeneous mixtures, substances, compounds, and elements... [Pg.2]

There is however a great and obvious need for a convenient term to refer to chiral substances fhat are composed of only one of the two enantiomers. Numerous terms for this purpose have been introduced over many years, but the issue remains complex and largely unresolved. The present author recently discussed this issue in detail and introduced a new term for the purpose unichiral [5]. In the present chapter unichiral will be used to specify fhe stereochemical composition of a chiral drug, substance, compound, sample, etc, as stereochemically homogeneous, i. e., consisting of a single-enantiomer (in the context where fhe term is used and wifhin the limits of measurement) [5]. [Pg.5]

According to the thermal/humidity stress testing conditions selected, samples are placed into appropriate ovens. If humidity ovens capable of 70°C/30% RH and 70°C/75% RH are not available, saturated salt solutions contained in desiccators can be used to control humidity accurately. These conditions are particularly useful for high-potency drug substance compounds for which samples must be contained. A saturated NaCl solution is used to obtain conditions of 75% RH at 70 °C and a saturated MgCl2 solution is used to obtain conditions of 30% RH at 70 °C. [Pg.102]

Note two additional Join clauses, each with the appropriate On clause naming the columns that relate the tables being joined. The additional columns compound id, compound type, and openeye can smiles are from the compound table. No columns are actually selected from the substance compound table. That table is simply used to affect the many-to-many relationship between the substance and compound tables. [Pg.60]

Finally, data about the compounds for each substance is also needed. The compound id is contained in the substance compound table. The SQL is extended to become... [Pg.65]


See other pages where Substance compounds is mentioned: [Pg.1023]    [Pg.180]    [Pg.239]    [Pg.78]    [Pg.7]    [Pg.3]    [Pg.63]    [Pg.60]    [Pg.875]    [Pg.10]    [Pg.363]    [Pg.289]    [Pg.97]    [Pg.56]    [Pg.308]    [Pg.137]    [Pg.402]    [Pg.102]    [Pg.10]    [Pg.13]    [Pg.15]    [Pg.145]    [Pg.95]    [Pg.21]    [Pg.164]    [Pg.60]    [Pg.61]   
See also in sourсe #XX -- [ Pg.33 ]

See also in sourсe #XX -- [ Pg.33 ]

See also in sourсe #XX -- [ Pg.33 , Pg.34 ]




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