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Bioassay of alternate molecular forms supports the view that the ORs are capable of resolving isomeric distinctions in neutral (non-biological) odourants. Stereochemical pairs of odours were tested for differential sensitivities in the blind subterranean mole rat (Spalax ehrenbergi). The subjects responded to one enantiomer, but not to its stereoisomer. Both sexes were attracted to the odour of R-(-)-carvone but unresponsive to S-(+)-carvone in contrast, males and females were repelled by the odour of (+)-citronellol, but not by (-)-citronellol (Heth et al., 1992). The lack of responsiveness by mole rats could be central due to lack of salience, or peripheral due to hyposmia/anosmia for one isomer. Both carvones have distinct odours for the human nose. [Pg.55]

One can think of metabolism similar to that of an automobile salvage operation. Useful parts are removed and used as replacement for worn out parts or put to an entirely different use, perhaps in a new configuration. Other parts may be stored for use at a later time and still others may be discarded. Thus, chemicals taken into the body are not necessarily used intact, but may be dismantled and reassembled within certain chemical limitations. An isolated molecule may become an integral part of the body in its original molecular form or it may be altered and incorporated in a new configuration. The body s system for doing this, however, is subject to error and potential breakdowns. [Pg.19]

Under ordinary conditions flames are transparent over a wide range of wavelengths, a fact found with surprise by Foucault in 1849 (S9) and probably by everyone else since with an interest in this subject. Most flame constituents are gases in atomic or molecular form, and whatever... [Pg.7]

It has already been pointed out that hydrazine is probably subject to attack by atomic hydrogen and in this connection it is interesting to note that an alternative technique in which atomic hydrogen is converted to the less reactive molecular form through the agency of a platinum catalyst has also shown increased yields of hydrazine (7). [Pg.393]

The same catalysts also made all-cis, fully head-to-tail biased, syndiotactic polymers from ( )-l-methylNBE. Such materials are alternating copolymers of enantiomers and in accord with expectation the resolved monomer refuses to polymerize with ReCls as catalyst [12]. In ROMP of these derivatives only the exo face of the olefmic bond is attacked, but there are two molecular forms in the racemic mixture. Subject to the... [Pg.50]

When subjected to an electron bombardment whose energy level is much higher than that of hydrocarbon covalent bonds (about 10 eV), a molecule of mass A/loses an electron and forms the molecular ion, the bonds break and produce an entirely new series of ions or fragments . Taken together, the fragments relative intensities constitute a constant for the molecule and can serve to identify it this is the basis of qualitative analysis. [Pg.48]

The Langmuir-Hinshelwood picture is essentially that of Fig. XVIII-14. If the process is unimolecular, the species meanders around on the surface until it receives the activation energy to go over to product(s), which then desorb. If the process is bimolecular, two species diffuse around until a reactive encounter occurs. The reaction will be diffusion controlled if it occurs on every encounter (see Ref. 211) the theory of surface diffusional encounters has been treated (see Ref. 212) the subject may also be approached by means of Monte Carlo/molecular dynamics techniques [213]. In the case of activated bimolecular reactions, however, there will in general be many encounters before the reactive one, and the rate law for the surface reaction is generally written by analogy to the mass action law for solutions. That is, for a bimolecular process, the rate is taken to be proportional to the product of the two surface concentrations. It is interesting, however, that essentially the same rate law is obtained if the adsorption is strictly localized and species react only if they happen to adsorb on adjacent sites (note Ref. 214). (The apparent rate law, that is, the rate law in terms of gas pressures, depends on the form of the adsorption isotherm, as discussed in the next section.)... [Pg.722]

It is recommended that the reader become familiar with the point-group symmetry tools developed in Appendix E before proceeding with this section. In particular, it is important to know how to label atomic orbitals as well as the various hybrids that can be formed from them according to the irreducible representations of the molecule s point group and how to construct symmetry adapted combinations of atomic, hybrid, and molecular orbitals using projection operator methods. If additional material on group theory is needed. Cotton s book on this subject is very good and provides many excellent chemical applications. [Pg.149]

Chlorine heptoxide is more stable than either chlorine monoxide or chlorine dioxide however, the CX C) detonates when heated or subjected to shock. It melts at —91.5°C, bods at 80°C, has a molecular weight of 182.914, a heat of vapori2ation of 34.7 kj/mol (8.29 kcal/mol), and, at 0°C, a vapor pressure of 3.2 kPa (23.7 mm Hg) and a density of 1.86 g/mL (14,15). The infrared spectmm is consistent with the stmcture O CIOCIO (16). Cl O decomposes to chlorine and oxygen at low (0.2—10.7 kPa (1.5—80 mm Hg)) pressures and in a temperature range of 100—120°C (17). It is soluble in ben2ene, slowly attacking the solvent with water to form perchloric acid it also reacts with iodine to form iodine pentoxide and explodes on contact with a flame or by percussion. Reaction with olefins yields the impact-sensitive alkyl perchlorates (18). [Pg.65]

Concretes and absolutes, both obtained by total extraction of the plant material and not subject to any form of distillation other than solvent removal, are complex mixtures containing many chemical types over wide molecular weight ranges. In some cases, gas chromatographic analysis shows httle volatile material. Yet these products have powerful odors and contribute in important ways to the perfumes in which they are used. [Pg.76]


See other pages where Subject molecular forms is mentioned: [Pg.159]    [Pg.65]    [Pg.891]    [Pg.117]    [Pg.1416]    [Pg.1943]    [Pg.194]    [Pg.425]    [Pg.256]    [Pg.60]    [Pg.341]    [Pg.500]    [Pg.533]    [Pg.12]    [Pg.424]    [Pg.439]    [Pg.890]    [Pg.656]    [Pg.228]    [Pg.366]    [Pg.425]    [Pg.244]    [Pg.110]    [Pg.661]    [Pg.265]    [Pg.36]    [Pg.350]    [Pg.353]    [Pg.419]    [Pg.161]    [Pg.320]    [Pg.361]    [Pg.180]    [Pg.351]    [Pg.439]    [Pg.86]    [Pg.208]    [Pg.238]    [Pg.244]    [Pg.252]    [Pg.1500]   
See also in sourсe #XX -- [ Pg.76 ]




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