Fr. 52.50

Stereoelectronic Effects

English · Paperback / Softback

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Zusatztext engaging critique of biography .... enjoyable and thought provoking Klappentext This series of short texts provides accessible accounts of a range of essential topics in chemistry. Written with the needs of the student in mind, the Oxford Chemistry Primers offer just the right level of detail for undergraduate study, and will be invaluable as a source of material commonly presented in lecture courses yet not adequately covered in existing texts. All the basic principles and facts in a particular area are presented in a clear and straightforward style, to produce concise yet comprehensive accounts of topics covered in both core and specialist courses. Stereoelectronic effects - interactions between electronic orbitals in three dimensions - control the way that molecules are put together and the 'rules of engagement' which operate when they meet and react. An understanding of these effects will help the student develop a 'feel' for the nature of molecules and their capabilities, which is especially useful when considering reactivity. Although there are a vast numbers of reactions known, these may be grouped into a small number of mechanistic classes, then into a still smaller set of classes of stereoelectronic interaction. Stereoelectronic effects is deliberately non-mathematical in its approach, with reactions illustrated by real examples. It should provide the student with an understanding of fundamental relationships and a powerful but simple approach to thinking about Chemistry. Zusammenfassung Describes how stereoelectronic effects control the rules of engagement that operate when molecules meet. Aimed at undergraduate students, this book gives a 'feel' or intuition for molecules and what they are capable of. The treatment is non-mathematical and the treatment shows the student building up a simple way of thinking about Chemistry. Inhaltsverzeichnis Introduction 1: The electronic basis of stereoelectronic effects 2: Effects on conformation 3: Effects on reactivity 4: Substitutions at saturated centres 5: Additions and eliminations 6: Rearrangements and fragmentations 7: Radical reactions ...

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