Transcription of A SN1 Reaction: Synthesis of tert-Butyl Chloride
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Supplementary information for Comprehensive organic Chemistry Experiments for the Laboratory Classroom The Royal Society of Chemistry 2017 A SN1 Reaction: Synthesis of tert-Butyl Chloride Supplementary Material Experiment Notes: This lab experiment proposes the Synthesis of an alkyl halide by reacting the corresponding alcohol with a hydrogen halide in an easy and inexpensive SN1 ,2 tert-Butanol reacts readily with HCl and forms the corresponding tert-Butyl Chloride at room temperature. SN1 mechanisms are unimolecular because its slow step is unimolecular.
nucleophile is not involved in the rate–determining step of the process a strong ... 1 K.P.C., Vollhardt, N.E. Schore, Organic Chemistry: Structure and Function, Freeman and Company, New York. 6th Ed, 2010 ... The compound is only sparingly soluble in water, but the ...
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