Abstract
Alkanes, with their strong, low polarity C—C and C—H bonds, rarely participate in ionic reactions unless some heteroatom is present. The common heteroatoms such as halogen, oxygen and nitrogen are all more electronegative than carbon. The substituted carbon atoms are therefore cationoid and susceptible to nucleophilic attack; hence the predominance of SN reactions in aliphatic chemistry.
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Bates, R. B., and Ogle, C. A. (1983). Carbanion Chemistry. Springer, Berlin
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Lowry, T. H., and Richardson, K. S. (1981). Mechanism and Theory in Organic Chemistry, 2nd edn. Harper and Row, New York
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© 1986 A. W. Parkins and R. C. Poller
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Parkins, A.W., Poller, R.C. (1986). Organometallic Compounds as Sources of Carbanions. In: An Introduction to Organometallic Chemistry. Palgrave, London. https://doi.org/10.1007/978-1-349-18198-8_4
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DOI: https://doi.org/10.1007/978-1-349-18198-8_4
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