Lecture 8 - Solvent, Leaving Group, Bridgehead Substitution, and Pentavalent Carbon

author: J. Michael McBride, Department of Chemistry, Yale University
recorded by: Yale University
published: Aug. 19, 2014,   recorded: February 2011,   views: 1386
released under terms of: Creative Commons Attribution No Derivatives (CC-BY-ND)
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The nature of nucleophiles and leaving groups has strong influence on the rate of SN2 reactions. Generally a good nucleophile or strong base is a poor leaving group, but hydrogen-bonding solvents can alter nucleophile reactivity. Although amino and hydroxyl groups are poor leaving groups, they may be converted to groups that leave easily, even from bridgehead positions. Designing the preparation of a sugar analogue containing radioactive fluorine shows how understanding the SN2 mechanism enables PET scanning for medical imaging. Quantum mechanics suggests that the pentavalent carbon species on the SN2 reaction pathway is a transition state, not a stable structure.

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