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Propane molecule

The parent compound of this family is methane. The propane molecule, with three carbon and eight hydrogen atoms, is third in the series after ethane (C Hf,). The specific gravity is 0.508-0.510 at 60°F (15.6°C). The melting point is -309.8°F (-189.9°C). (See Table 1 for other selected properties of LP-gases.)... [Pg.721]

On the other hand, the formation of ethylene was ascribed mainly to the unimolecular decomposition of a neutral excited propane molecule. These interpretations were later confirmed (4) by examining the effect of an applied electrical field on the neutral products in the radiolysis of propane. The yields of those products which were originally ascribed to ion-molecule reactions remained unchanged when the field strength was increased in the saturation current region while the yields of hydrocarbon products, which were ascribed to the decomposition of neutral excited propane molecules, increased several fold because of increased excitation by electron impact. In various recent radiolysis 14,17,18,34) and photoionization studies 26) of hydrocarbons, the origins of products from ion-molecule reactions or neutral excited molecule decompositions have been determined using the applied field technique. However, because of recent advances in vacuum ultraviolet photolysis and ion-molecule reaction kinetics, the technique used in the above studies has become somewhat superfluous. [Pg.272]

The convenience and usefulness of the concept of resonance in the discussion of chemical problems are so great as to make the disadvantage of the element of arbitrariness of little significance. Also, it must not be forgotten that the element of arbitrariness occurs in essentially the same way in the simple structure theory of organic chemistry as in the theory of resonance — there is the same use of idealized, hypothetical structural elements. In the resonance discussion of the benzene molecule the two Kekule structures have to be described as hypothetical it is not possible to synthesize molecules with one or the other of the two Kekule structures. In the same way, however, the concept of the carbon-carbon single bond is an idealization. The benzene molecule has its own structure, which cannot be exactly composed of structural elements from other molecules. The propane molecule also has its own structure, which cannot be composed of structural elements from other molecules — it is not possible to isolate a portion of the propane molecule, involving parts of two carbon atoms... [Pg.14]

To take care of the three carbon atoms per propane molecule, we need three molecules of CO2. Thus, the carbon atoms are balanced by changing the stoichiometric coefficient of CO2 from 1 to 3. In this reaction the ratio of CO2 to propane is 3 1. Similarly, we need four molecules of water for the eight hydrogen atoms in one molecule of propane. Using this information, we modify the equation as follows ... [Pg.203]

To estimate the amount of energy absorbed or released in this reaction, we must compile an inventoiy of all the bonds that break and all the bonds that form. A ball-and-stick model shows that propane contains 8 C—H bonds and 2 C—C bonds. These bonds break in each propane molecule, and one ODO bond breaks in each oxygen molecule. Two CDO bonds form in each CO2 molecule, and two O—H bonds form in each H2 O molecule. In summary ... [Pg.384]

More recently, enzymatic carboligation in a solid/gas bioreactor was demonstrated to be possible [55] in a model system based on the condensation of two propanal molecules to produce of propioin using thiamine diphosphate-dependent... [Pg.274]

Nicholas et al. (67) have performed MD calculations of propane in sili-calite in which the propane molecule is given complete flexibility. The calculations, which have been detailed previously for methane diffusion, employed a large simulation box with multiple sets of adsorbates to ensure good statistics. The framework was kept fixed and data were collected over a 40-ps run. The results predict diffusion coefficients in very good agreement with the values of Caro et al. (71). The calculated values for a concentration of 4 and 12 propane molecules per silicalite unit cell are 0.12 and 0.005 X 10 8 m2/s, respectively. These values for propane are far lower than those of Nowak et al. (63), the reason for this is that Nicholas et al. used flexible adsorbate molecules, whereas Nowak et al. used rigid ones. [Pg.36]

Preferential sorption in the sinusoidal channels was confirmed by Nicholas et al. (67) in an MD study of methane and propane adsorption. This preference was most noticeable at infinite dilution at a loading of 12 molecules per unit cell the distribution of molecules over the channels was found to be close to that expected from the relative volumes of the channel segments. The propane molecules were predicted to spend more time in the intersections than the straight channel at infinite dilution. This result is rationalized by considering the slow motion of the molecules and the conformational changes necessary to move from one channel type to another via an intersection. The distribution of propane backbone bond angles was predicted to be similar to that of gas-phase propane, indicating the rather minor effect of the zeolite on the internal coordinates of propane. [Pg.71]

Figure 4 Temperature dependence of the experimental self-diffusion coefficient of propane molecules in NaX. Figure 4 Temperature dependence of the experimental self-diffusion coefficient of propane molecules in NaX.
We can therefore write the detailed reaction path for the mercury-photosensitized decomposition of the propane molecule as follows ... [Pg.267]

Experimental evidence of the part played by free radicals in a chemical reaction was soon forthcoming. In 1934 Frey24 found that butane decomposed very slowly at 525° but that if one per cent of dimethyl mercury was introduced the decomposition proceeded rapidly. In the same year Sickman and Allen25 found that acetaldehyde was stable at 300° but that it was decomposed completely when a few per cent of azomethane was added. The introductions of dimethyl mercury or azomethane at these temperatures apparently liberated free radicals which initiated chains. Moreover when mixed gases decomposed simultaneously they did not do so independently. The products contained groups from each in a way that could be easily explained on the assumption of the liberation and recombination of free radicals. Again the appearance of butane from the decomposition of propane is difficult to explain on any hypothesis except on the assumption that some free radicals of CH3 are split out and that they become attached to propane molecules. More direct examples will be given later in the discussion of photochemistry. [Pg.51]

The correct answer is (A). The propane molecule is essentially nonpolar. The polar OH bond in propanol allows for the formation of hydrogen bonds that will increase its boiling point. [Pg.125]

Such a large difference in boiling points suggests that ethanol molecules are attracted to each other much more strongly than propane molecules. Two important inter-molecular forces are responsible hydrogen bonding and dipole-dipole attractions (Section 2-10). [Pg.431]

Figures 42 and 43 show scanning electron micrographs of two ZSM-5 samples of different configurations coffin-shaped crystals and polycrystalline grains. To emphasize the relationship between sample dimensions and diffusion paths followed during the PFG NMR experiment, magnifications are referenced against typical root mean square displacements for methane and propane molecules during typical PFG NMR observation times. Figures 42 and 43 show scanning electron micrographs of two ZSM-5 samples of different configurations coffin-shaped crystals and polycrystalline grains. To emphasize the relationship between sample dimensions and diffusion paths followed during the PFG NMR experiment, magnifications are referenced against typical root mean square displacements for methane and propane molecules during typical PFG NMR observation times.
The resulting radicals can abstract from propane molecules with the formation of normal and isopropyl radicals, viz. [Pg.53]


See other pages where Propane molecule is mentioned: [Pg.382]    [Pg.178]    [Pg.296]    [Pg.15]    [Pg.122]    [Pg.23]    [Pg.78]    [Pg.58]    [Pg.140]    [Pg.251]    [Pg.252]    [Pg.185]    [Pg.34]    [Pg.341]    [Pg.14]    [Pg.265]    [Pg.268]    [Pg.223]    [Pg.191]    [Pg.82]    [Pg.15]    [Pg.63]    [Pg.217]    [Pg.214]    [Pg.290]    [Pg.266]    [Pg.272]    [Pg.54]    [Pg.69]    [Pg.145]    [Pg.199]    [Pg.406]    [Pg.3119]    [Pg.65]    [Pg.124]   


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