Carbon compound structural formulae

Why is potassium aluminium sulphate not soluble in benzene A compound M has the composition C = 50.0% H=12.5%o A1 = 37.5%. 0.360 g of M reacts with an excess of water to evolve 0.336 1 of gas N and leave a white gelatinous precipitate R. R dissolves in aqueous sodium hydroxide and in hydrochloric acid. 20 cm of N require 40 cm of oxygen for complete combustion, carbon dioxide and water being the only products. Identify compounds N and R, suggest a structural formula for M, and write an equation for the reaction of M with water. (All gas volumes were measured at s.t.p.)... 

This reference work differs from Beilstein in that it is baaed upon structural formulae and compounds are grouped according to the carbon skeleton rather than the functional group the latter system has the advantage that closely related compounds are grouped together. The volumes are not published in numerical order but rather on the basis of fields of current interest. They are a valuable supplement to Beilstein. The volumes which have been published to date (1955) are ... 

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. 

Note that these compounds are covalently bonded compounds containing only hydrogen and carbon. The differences in their strucmral formulas are apparent the alkanes have only single bonds in their structural formulas, while the alkenes have one (and only one) double bond in their structural formulas. There are different numbers of hydrogen atoms in the two analogous series. This difference is due to the octet rule that carbon must satisfy. Since one pair of carbon atoms shares a double bond, this fact reduces the number of electrons the carbons need (collectively) by two, so there are two fewer hydrogen atoms in the alkene than in the corresponding alkane. 

Note that there is no one-carbon alkene corresponding to methane, since hydrogen can never form more than one covalent bond, and there is no other carbon atom in the structural formula. Therefore, the first compound in the alkene series is ethene, while the corresponding two-carbon compound in the alkane series, ethane, is the second compound in the series, with methane the first. 

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. 

In the realm of chemical enumeration we note Polya s equation (4.4) which gives the generating function for stereoisomers of the alkyl radicals, or equivalently, alcohols — that is, equation (5.2) of this article. His equation (4.3) gives the corresponding result for the structural isomers of these compounds. His equations (4.2) and (4.5) correspond, respectively, to the cases of alcohols without any asymmetric carbon atoms and the number of embeddings in the plane of structural formulae for alcohols in general. The latter problem is not chemically very significant. 

We have now found all possible structural formulas for the ethanol molecule. The oxygen atom is either directly bonded to one carbon atom or to two carbon atoms. Once a choice between these two possibilities is made, the structure of the rest of the molecule can be determined from the molecular formula and the bonding rules. The two possible structures are shown in Figure 18-2. Such compounds with the same molecular formula but different structural formulas are called structural isomers. The existence of the two compounds I and 2 was known long before their structures were clarified. Hence the existence of these isomers perplexed chemists for decades. Now we recognize the crucial impor-... 

Ethylene glycol has empirical formula CH30 and molecular formula C2H602. Using the usual bonding rules (carbon is tetravalent oxygen is divalent hydrogen is monovalent), draw some of the structural formulas possible for this compound. 

By far the majority of the million or so known compounds of carbon also contain hydrogen and oxygen. There are several important types of oxygen-containing organic compounds and they can be studied as an oxidation series. For instance, the compound methanol, CH3OH, is very closely related to methane, as their structural formulas show. Methanol can be regarded as the first step in the complete oxidation of methane to carbon dioxide and water. 

If the sample consists of atoms of one element, the mass spectrum gives the isotopic distribution of the sample. The relative molar masses of the isotopes can be determined by comparison with atoms of carbon-12. If the sample is a compound, the formula and structure of the compound can be determined by studying the fragments. For example, the + 1 ions that CH4 could produce are CH4, CH3+, CH, CFI4, C+, and H4. Some of the particles that strike the detector are those that result when the molecule simply loses an electron (for example, to produce Cl I4+ from methane) ... 

Each line in a structural formula represents one pair of shared electrons, but atoms can share more than one pair of electrons. When two atoms share one pair of electrons, the bond is called a single bond, and the structural formula shows a single line. When two atoms share four electrons, the bond is called a double bond, and the structural formula shows two lines between the atoms. Similarly, when two atoms share six electrons, the bond is called a triple bond, and the stmctural formula shows three lines between the atoms. Two carbon atoms can bond to each other through any of these three kinds of bonds, as the compounds in Figure illustrate. 

The chemistry of living processes is complex, and many carbon-based molecules found in living organisms have extremely complicated stmctures. Because of this complexity, chemists have developed line structures, which are compact representations of the stmctural formulas of carbon compounds. Line structures are constructed according... 

Methane, CH4, has one carbon atom. The next two members of the alkane family are ethane, C2H6, and propane, C3H8. Molecules of these compounds contain chains of two carbon atoms and three carbon atoms, respectively. Alkanes with more than three carbon atoms have more than one isomer. There are two structural formulas for butane, C4H10, and three structural formulas for pentane, C5H12. 

The ability of a carbon atom to link to more than two other carbon atoms makes it possible for two or more compounds to have the same molecular formula but different structures. Sets of compounds related in this way are called isomers of each other. For example, there are two different compounds having the molecular formula C4HI0. Their structural formulas are as follows ... 

Figure 6. Structural formulae of S-D amphiphilic compounds and other chemicals used for S-D monolayers for comparison of photo-induced electron transfer rates between a single alkyl chain and a triple alkyl chain as the spacers of the S-D dyads with the same length of four-carbons. In these S-D dyads, a naphthalene and a ferrocene moiety are used as an S and a D moiety, respectively. S-D dyads with a rigid spacer consisting of a bicyclo[2.2.2]octane are used as dyads with a triple alkyl chain.

Compounds that have the same molecular formulas, but different structural formulas, are isomers. When dealing with hydrocarbons, this amounts to a different arrangement of the carbon atoms. Isomers such as these are structural isomers. 

Isomers are compounds that have the same molecular formulas but different structural formulas. Review the writing of the various structural isomers of alkanes. Make sure that each carbon atom has four bonds. 

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