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Conformation,in solution,of c-4-t-butyl-1-phenyl-r-1-(N-piperidyl)cyclohexane hydrochloride. The conformational energy of t-butyl
Authors:Muthiah Manoharan  Ernest L. Eliel
Affiliation:William Kenan, Jr. Laboratories of Chemistry, University of North Carolina Chapel Hill, NC 27514 USA
Abstract:Although the hydrochloride of c-4-t-butyl-1-phenyl-c-1-(N-piperidyl)cyclohexane crystallizes in the conformation with axial t-butyl, it exists as an almost equimolar mixture of the two chair conformers in CD2 Cl2 solution. The position of equilibrium allows one to calculate ΔG°t-Bu as ?4.9 kcal/mol.
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