Carbon atoms structural properties

Although alkanes are not as reactive as other classes of organic compounds, they have many of the same structural characteristics. We will use simple alkanes as examples to study some of the properties of organic compounds, including the structure of sjf hybridized carbon atoms and properties of C—C and C—H single bonds. 

If you think that the structures represent two different substances, you are right. The structure on the left represents butane, and the structure on the right represents a branched-chain alkane, known as isobutane, a substance whose chemical and physical properhes are different from those of butane. As you see, carbon atoms can bond to one, two, three, or even four other carbon atoms. This property makes possible a variety of branched-chain alkanes. How do you name isobutane using lUPAC rules ... 

These two structures could only be interconverted through rotation of one of the —CHCl gronps by 180° abont the C=C bond axis. This wonld necessitate the breaking of the TT bond between the two carbon atoms. The properties of the two molecules are quite different. As discnssed in Section 4.2, the cis isomer has a relatively large dipole moment (1.89 D), whereas the more symmetric trans isomer has a dipole moment of zero. This difference is reflected in the boihng points, which are 333.5 K and 320.7 K for the cis and trans isomers, respectively. 

Because of the existence of numerous isomers, hydrocarbon mixtures having a large number of carbon atoms can not be easily analyzed in detail. It is common practice either to group the constituents around key components that have large concentrations and whose properties are representative, or to use the concept of petroleum fractions. It is obvious that the grouping around a component or in a fraction can only be done if their chemical natures are similar. It should be kept in mind that the accuracy will be diminished when estimating certain properties particularly sensitive to molecular structure such as octane number or crystallization point. 

This structure indicates that carbon monoxide should have donor properties, the carbon atom having a lone pair of electrons. Carbon... 

Alternatively the ion exchanger may be a synthetic polymer, for example a sulphonated polystyrene, where the negative charges are carried on the —SO3 ends, and the interlocking structure is built up by cross-linking between the carbon atoms of the chain. The important property of any such solid is that the negative charge is static—a part of the solid—whilst the positive ions can move from their positions. Suppose, for example, that the positive ions are... 

A particularly good selection of physical properties may be spectra, because they are known to depend strongly on the chemical structure. In fact, different types of spectra carry different kinds of structural information, NMR spectra characterize individual carbon atoms in their molecular environment. They therefore correspond quite closely to fragment-based descriptors, as underlined by the success of approaches to predict NMR spectra by fragment codes (see Section 10.2.3). 

Within each analogous series of hydrocarbons there exist isomers of the compounds within that series. An isomer is defined as a compound with the same molecular formula as another compound but with a different structural formula. In other words, if there is a different way in which the carbon atoms can align themselves in the molecule, a different compound with different properties will exist. 

With the five-carbon alkane, pentane, there are three ways to draw the structural formula of this compound with five carbon atoms and twelve hydrogen atoms. The isomers of normal pentane are isopentane and neopentane. The structural formulas of these compounds are illustrated in Table 2, while typical properties are given in Table 1. 

As in the alkanes, it is possible for carbon atoms to align themselves in different orders to form isomers. Not only is it possible for the carbon atoms to form branches which produce isomers, but it is also possible for the double bond to be situated between different carbon atoms in different compounds. This different position of the double bond also results in different structural formulas, which, of course, are isomers. Just as in the alkanes, isomers of the alkenes have different properties. The unsaturated hydrocarbons and their derivatives are more active chemically than the saturated hydrocarbons and their derivatives. 

Alicyclic Hydrocarbons. These refer to cyclic analogues of aliphatic hydrocarbons and are named accordingly, using the piefix cyclo-." Their properties are similar to their open-chain aliphatic counterparts. Alicyclic hydrocarbons are subdivided into monocyclic (cycloalkanes, cycloalkenes, cycloalkynes, cycloalkadienes, etc.) and polycyclic aliphatic compounds. Monocyclic aliphatic structures having more than 30 carbon atoms in the ring are known, but those containing 5 or 6 carbon atoms are more commonly found in nature [47, p. 28]. 

In these line-angle formulas it is understood that there is a carbon atom at each vertex of the hexagon hydrogen atoms are not shown. This model is consistent with many of the properties of benzene. The molecule is a planar hexagon with bond angles of 120°. The hybridization of each carbon is sp2. However, this structure is misleading in one respect Chemically, benzene does not behave as if double bonds were present... 

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