Section 1 Simple Organic Compounds

Before I proceed with the discussion of the dediazoniation mechanism, it is necessary to spend some paragraphs considering the definition of the term crisis as used by Kuhn. As already discussed in Section 8.3 the crisis was terminated by the experiments which demonstrated that the first step in Scheme 9-2 is reversible (mechanism B), or in other words that a simple organic compound, the phenyl cation, does react with N2 molecules. 

There are millions of organic compounds many consist of highly intricate molecules, so their names can be very complicated. You could, for example, find yourself asking for ct-D-glucopyranosyl(l—>2)-(3-D-fructofuranose when all you wanted was sucrose (sugar). However, for most of this text, we will need to know only a few simple organic compounds, and this section will introduce some of them. Chapters 18 and 19 present a more complete introduction to the nomenclature of organic compounds. 

Many types of organic compounds exhibit characteristic mass spectral behaviour, a knowledge of which is useful in the interpretation of their spectra. The following section provides an introduction to the interpretation of mass spectra of simple organic compounds but readers should consult the texts listed in the references.4 Some caution is needed in the application of this information since... 

Because monosaccharides contain alcohol functional groups and aldehyde (or ketone) functional groups, the reactions of monosaccharides are an extension of what you have already learned about the reactions of alcohols, aldehydes, and ketones. For example, an aldehyde group in a monosaccharide can be oxidized or reduced and can react with nucleophiles to formimines, hemiacetals, and acetals. When you read the sections that deal with the reactions of monosaccharides, you will find cross-references to the sections in which the same reactivity for simple organic compounds is discussed. As you study, refer back to these sections they will make learning about carbohydrates a lot easier and will give you a good review of some chemistry that you have already learned about. 

Naming Inorganic Compounds Some Simple Organic Compounds (Sections 2.8 and 2.9)... 

The application of mixed melting point determinations to the identification of organic compounds has been described in Section 1,17. In order to gain experience the student should carry out the following simple experiment. 

Hydrolysis is an enzymatic process by which complex organic compounds that cannot directly be used as substrates by the bacterial biomass can be broken down into simple molecules (see Section 3.2.3). The complex hydrolyzable... 

Two patterns are possible in the activation mechanism by simple chiral Lewis base catalysts. One is through the activation of nucleophiles such as aUyltrichlorosilanes or ketene trichlorosilyl acetals via hypervalent silicate formation using organic Lewis bases such as chiral phosphoramides or A-oxides. " In this case, catalysts are pure organic compounds (see Chapter 11). The other is through the activation of nucleophiles by anionic Lewis base conjugated to metals. In this case, transmetal-lation is the key for the nucleophile activation. This type of asymmetric catalysis is the main focus of this section. 

As described in Section 4.1.2, electrophilic organic compounds are reducible at the electrode. Some reducible organic compounds are listed in Table 8.5 with the potentials of the first reduction step in dipolar aprotic solvents. As described in Ref. [47], organic compotinds undergo various complicated electrode reductions. Here, however, only simple but typical cases are considered they are reductions of the outer sphere type and the dissociative electron transfer reactions. 

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