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Butane skeletal structure

The following facts are the basis for butene isomerization (I) There is a basic similarity in the composition of alkylates produced from all four butene isomers. (2) Alkylate molecules, once formed, are relatively stable under alkylation conditions and do not isomerize to any appreciable extent alkylate fractions having the same carbon number ore not equilibrated (see Table I). (3) Thermodynamic equilibrium between the butene olefins highly favors isobutene formation at alkylation temperatures. (4) Normal butenes p>roduce only small and variable amounts of normal butane, thus indicating only a small and variable amount of chain initiation from normal butenes. Yet the alkylate composition shows a high concentration of trimethylpentanes and a low concentration of dimethylhexanes. (5) A few of the octane isomers can be explai.ned only by isomerization of the eight-carbon skeletal structure this isomerization occurs while isobutene dimer is in ionic form. For example, 2,3,3- and 2,3,4-trimethylpentanes... [Pg.31]

Both titania (anatase more than rutile) and, even more, zirconia (tetragonal more than monoclinic), when sulfated or covered with tungsten oxide become very active for some hydrocarbon conversion reactions such as -butane skeletal isomerization [263]. For this reason, a discussion began on whether these materials have to be considered superacidic. Spectroscopic studies showed that the sulfate ions [264] as well as the tungstate ions [265,266] on ionic oxides in dry conditions, are tetracoordinated with one short S=0 and W=0 bond (mono-oxo structure) as shown in Scheme 9.3(11). Polymeric forms of tungstate species could also be present [267]. However, in the presence of water the situation changes very much. According to the Lewis acidity of wolframyl species, it is believed that it can react with water and be converted in a hydrated form, as shown in Scheme 9.3. Residual... [Pg.296]

These three chi indexes are not highly intercorrelated. The x index encodes size and branching information. The index encodes even more specific information about skeletal branching, x increases with the increase in skeletal branching in the hexane series the x values increase in the order hexane < 3-methylpentane, < 2-methylpentane, < 2,3-dimethylbutane, < 2,2-dimethyl-butane. The Xpc index is sensitive to specific structural aspects, especially to gem and vicinal substitution patterns. The negative sign on Xpc reflects a... [Pg.382]

Draw the expanded structural formula, condensed stractural formula, aud skeletal formula for butane. [Pg.197]


See other pages where Butane skeletal structure is mentioned: [Pg.1123]    [Pg.331]    [Pg.23]    [Pg.413]    [Pg.67]    [Pg.186]    [Pg.58]    [Pg.333]   
See also in sourсe #XX -- [ Pg.102 ]




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Butane structure

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