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1.3- Dipoles nitrous oxide

Let us turn to the results obtained for nitrous oxide N2O. From a theoretical point of view, this is an interesting molecule as properties such as its dipole moment and protonation site have been found very difficult to calculate accurately [14,24], N2O is a linear species whose predicted bond lengths and dipole moment are presented in Table 2. [Pg.222]

In Section 4.2 an analysis based on bond lengths and dipole moments was presented showing that structures I and II contribute about equally to the actual structure. Nitrous oxide functions as an oxidizing agent that can react explosively with H2,... [Pg.489]

The ability of nitrous oxide to forma 1,3-dipole (Section 7.2) seems to be of critical importance for the reaction with alkenes. The oxygen transfer proceeds via the 1,3-dipolar cycloaddition mechanism, assuming intermediate formation of a 1,2,3-oxadiazoline complex, the decomposition of which leads to a carbonyl compound ... [Pg.232]

Nitrous oxide has a small molecular dipole, but it is not very polar compared to water. Therefore, nitrous oxide is expected to be preferentially soluble in adipose tissue. [Pg.399]

The carbonyl sulfide calculations were not as straightforward as the 2D nitrous oxide work. One issue is that the transition involves three transition dipoles to various states, whereas in nitrous oxide the absorption is dominated by a single transition. The calculation for OCS only considered a single transition. In addition the quality of the potential energy surfaces was not as high, and the 2D approximation not as good, for OCS relative to NNO. An illustration of this is that the predicted OCS spectrum has a maximum at 214 nm while the experimental spectrum has a maximum at 223 nm. In comparison the difference in peak location for NNO was only 3 nm. [Pg.125]

Water is also included in the table to make one point— the solvent that we are all most familiar with is a poor candidate from both engineering and safety standpoint. The critical temperature and pressure are among the highest for common solvents. Ammonia is very unpleasant to work with since a fume hood or other venting precautions are needed to keep it out of the laboratory atmosphere. One of the alternative fluids of potential interest is nitrous oxide. It is attractive since it has molecular weight and critical parameters similar to carbon dioxide, yet has a permanent dipole moment and is a better solvent than carbon dioxide for many solutes. There are evidences of violent explosive reactions of nitrous oxide in contact with oils and fats. For this reason, nitrous oxide should be used with great care and is not suitable as a general purpose extraction fluid. [Pg.16]

Nitrous oxide, N2O. This molecule is linear and its electric dipole moment is close to zero (017 D). Because of the similar scattering powers of N and 0 it is not possible to distinguish by electron diffraction between the alternatives NNO and NON, but the former is supported by spectroscopic data. X-ray diffraction data... [Pg.650]

CO2 and NjO are isoelectronic, linear triatomics with similar molecular weights, melting temperatures and quadrupole moments. Although NjO has no inversion symmetry, it has been shown to resonate between two bonding configurations with opposing dipole moments N=N =0 and N= N =0 [88]. As a result, the net dipole moment of nitrous oxide is negligible... [Pg.178]

Both of these configurations are clearly strongly polar, and if resonance implied that the resultant configuration was a mixture of the component structures nitrous oxide would show a large dipole moment. In fact, the moment is very small, as would be expected if the two structures, the polarities of which are opposed, contributed nearly equally to the resonance configuration. [Pg.66]

Fig 8 5 For nitrous oxide, the structure (a) is impossible because the molecule is linear, and the structures (b) and (c) may both participate because the dipole moment of the molecule is almost zero... [Pg.84]

Carbon dioxide adsorption on li-X, Na-X and K-X was investigated via IR already in 1963 by Bertsch and Habgood [202]. N2O and CO2 are also isoelectronic compounds. Moreover, the molecules of both compounds are linear, have a similar shape and identical mass the dipole moment of N2O is small (0.167 debye), that of CO2 is zero the three fundamentals of their internal vibrations fall in the same range of wavenumbers [636-638] (cf. also [640]). However, due to the lower symmetry, nitrous oxide molecules possess more possibilities of orientation [596]. [Pg.119]

Type III There is an overlapping of the low-lying LUMO of the dipole with the HOMO of the dipolarophiles. Such a situation is often referred to as a LUMO-controlled dipole or an electrophilic dipole and includes nitrous oxide and ozone. There is a close similarity of these reactions with an inverse electron-demand Diels—Alder reaction, which involves the overlapping of the diene LUMO and HOMO of the dienophile. [Pg.249]

For the four chnical anesthetics, d i,(z) exhibits minima at the interface. Thus, all these molecules are inter-facially active. However, the degree to which they tend to accumulate at the interface differs. For cyclopropane and nitrous oxide, the depths of the interfacial minima in measured with respect to the free energy in hexane, is smaller than 1 kcal/mol. The minima for isoflurane and desflurane are considerably deeper, approximately 2-2.5 kcal/mol. The interfacial activity of the solutes can be related to their polarity. Isoflurane and desflurane have an average permanent dipole moment of approximately 2 D. In contrast, cyclopropane is a symmetrical molecule with no permanent dipole moment, and the dipole moment of nitrous oxide is only 0.2 D. In spite of their small dipole moments, however, these molecules should be considered as weakly polar rather than non-polar. They are involved in non-negligible electrostatic interactions with water, that are primarily due to higher molecular multipole moments arising from substantial partial charges on the atoms. [Pg.41]

The structure of nitrous oxide is given below. Place the individual bond dipole moments on the diagram. Would the N O stretching vibration absorb infrared radiation ... [Pg.319]


See other pages where 1.3- Dipoles nitrous oxide is mentioned: [Pg.635]    [Pg.826]    [Pg.212]    [Pg.613]    [Pg.186]    [Pg.1051]    [Pg.84]    [Pg.85]    [Pg.131]    [Pg.208]    [Pg.618]    [Pg.39]    [Pg.618]    [Pg.160]    [Pg.677]   
See also in sourсe #XX -- [ Pg.1060 ]




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