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Weak varieties

The weak hydrogen bond, case 1, is a double minimum - high barrier in which the proton s motion is approximately harmonic and the deuteron s more so. Their motions are centred around the same point so that their shielding is roughly the same and thus there is no change in 6 on going from one to the other. The vast majority of hydrogen bonds are of this weak variety. [Pg.166]

Most chemical detonations are thought to be Chapman Jouguet detonations or, if supported by the boundary conditions, to be strong detonations. Weak detonations are not usually considered attainable because of the large reaction rates required, although there is some evidence that they exist in special circumstances. Vapor detonations, by contrast, are essentially all of the weak variety because of the nature of the equation of state, independently of the reaction rate. [Pg.408]

The high acidity of superacids makes them extremely effective pro-tonating agents and catalysts. They also can activate a wide variety of extremely weakly basic compounds (nucleophiles) that previously could not be considered reactive in any practical way. Superacids such as fluoroantimonic or magic acid are capable of protonating not only TT-donor systems (aromatics, olefins, and acetylenes) but also what are called (T-donors, such as saturated hydrocarbons, including methane (CH4), the simplest parent saturated hydrocarbon. [Pg.100]

Lipids differ from the other classes of naturally occurring biomolecules (carbohy drates proteins and nucleic acids) in that they are more soluble m nonpolar to weakly polar solvents (diethyl ether hexane dichloromethane) than they are m water They include a variety of structural types a collection of which is introduced m this chapter... [Pg.1069]

This relationship between and Kb simplifies the tabulation of acid and base dissociation constants. Acid dissociation constants for a variety of weak acids are listed in Appendix 3B. The corresponding values of Kb for their conjugate weak bases are determined using equation 6.14. [Pg.143]

The approach that we have worked out for the titration of a monoprotic weak acid with a strong base can be extended to reactions involving multiprotic acids or bases and mixtures of acids or bases. As the complexity of the titration increases, however, the necessary calculations become more time-consuming. Not surprisingly, a variety of algebraic and computer spreadsheet approaches have been described to aid in constructing titration curves. [Pg.284]

Directions are provided in this experiment for determining the dissociation constant for a weak acid. Potentiometric titration data are analyzed by a modified Gran plot. The experiment is carried out at a variety of ionic strengths and the thermodynamic dissociation constant determined by extrapolating to zero ionic strength. [Pg.359]

Fruit Juices nd Concentrates. Because fmit juices (qv) contain large amounts of water, they are often concentrated via evaporation (qv) followed by vacuum distillation. These compounds, especially ones of the citms variety, are widely used by the beverage industry. Many fmit juices, because of weak flavor, are augmented with other natural flavors (WONF), and are labeled as such (51). [Pg.440]

Vinylation. Acetylene adds weak acids across the triple bond to give a wide variety of vinyl derivatives. Alcohols or phenols give vinyl ethers and carboxyHc acids yield vinyl esters (see Vinyl polymers). [Pg.374]

Phthalocyanine Blues. a-Copper phthalocyanine blue is a reddish species used primarily in coatings and plastics. Several varieties are marketed. The basic form, the unstable Pigment Blue 15 [147-14-8] (Cl 74160), is used in water-based paints, paints containing weak petroleum solvents, and in certain plastics, eg, PVC, that require mild processing conditions. [Pg.506]

The Co nucleus decays with a half-life of 5.27 years by /5 emission to the levels in Ni. These levels then deexcite to the ground state of Ni by the emission of one or more y-rays. The spins and parities of these levels are known from a variety of measurements and require that the two strong y-rays of 1173 and 1332 keV both have E2 character, although the 1173 y could contain some admixture of M3. However, from the theoretical lifetime shown ia Table 7, the E2 contribution is expected to have a much shorter half-life and therefore also to dominate ia this decay. Although the emission probabilities of the strong 1173- and 1332-keV y-rays are so nearly equal that the difference cannot be determined by a direct measurement, from measurements of other parameters of the decay it can be determined that the 1332 is the stronger. Specifically, measurements of the continuous electron spectmm from the j3 -decay have shown that there is a branch of 0.12% to the 1332-keV level. When this, the weak y-rays, the internal conversion, and the internal-pair formation are all taken iato account, the relative emission probabilities of the two strong y-rays can be determined very accurately, as shown ia Table 8. [Pg.450]

Relatively high (typically 980—1200°C) temperatures are required to decompose spent acids at reasonable burner retention times. Temperatures depend on the type of spent acid. A wide variety of spent acids can be processed in this way, but costs escalate rapidly when the sulfuric acid concentration in spent acid (impurity-free basis) falls below about 75%. A few relatively uncontaminated spent acids can be reused without decomposition by evaporating the excess water in concentrators, or by mixing in fresh sulfuric acid of high concentration. Weak spent acids are frequently concentrated by evaporation prior to decomposition. [Pg.184]

A variety of other substances can provide the same reaction sulfur yields hydrogen sulfide chlorine yields hydrogen chloride. In some cases, some of the bonds created are quite weak resulting ia, after an iaduction period, a phenomenon termed "fallback." When fallback occurs, usually at a time when the hardened or oxidized asphalt is stored at or near the original processing or reaction temperature, softening of the asphalt is the result (28—31). [Pg.364]

R can be a variety of stmctures. Z is a leaving group and typically the conjugate base of a weak acid whose piC can range from 5 to 20 (86). The hydrogen peroxide is typically incorporated into the bath by a dding a soHd source of peroxide such as sodium percarbonate or the mono- or tetrahydrate of sodium perborate (86). [Pg.146]


See other pages where Weak varieties is mentioned: [Pg.97]    [Pg.132]    [Pg.97]    [Pg.132]    [Pg.384]    [Pg.1233]    [Pg.1786]    [Pg.2059]    [Pg.2159]    [Pg.2615]    [Pg.293]    [Pg.1147]    [Pg.293]    [Pg.236]    [Pg.102]    [Pg.464]    [Pg.375]    [Pg.441]    [Pg.151]    [Pg.134]    [Pg.34]    [Pg.246]    [Pg.368]    [Pg.412]    [Pg.243]    [Pg.443]    [Pg.226]    [Pg.429]    [Pg.445]    [Pg.72]    [Pg.320]    [Pg.66]    [Pg.68]    [Pg.338]    [Pg.17]    [Pg.346]    [Pg.257]   
See also in sourсe #XX -- [ Pg.201 ]




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