N.M.R. Experiments on Ketals Part I. Reaction Heat and Entropy of the Methyl Ketal Formation of Cyclohexanone, Cyclopentanone and Cyclobutanone
M. Anteunis, F. C. Alderweireldt, M. Acke
Abstract
M. Anteunis, F. C. Alderweireldt, M. Acke
Abstract
Abstract The methyl ketal formation is strongly exothermic (‐14,6 Kcal/mole) with cyclohexanone and moderately so with cyclopentanone (‐3,5 Kcal/mole) and with cyclobutanone (‐2,5 Kcal/mole). An exceptional low reaction entropy is noted for cyclohexanone (‐59 E.U.) and this is partly ascribed to the occurence of a high proportion of the twist conformation in cyclohexanone.
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Abstract The methyl ketal formation is strongly exothermic (‐14,6 Kcal/mole) with cyclohexanone and moderately so with cyclopentanone (‐3,5 Kcal/mole) and with cyclobutanone (‐2,5 Kcal/mole). An exceptional low reaction entropy is noted for cyclohexanone (‐59 E.U.) and this is partly ascribed to the occurence of a high proportion of the twist conformation in cyclohexanone.
Key concepts: Cyclopentanone, Cyclohexanone, Cyclobutanone, Chemistry, Exothermic reaction, Entropy (arrow of time), Organic chemistry, Medicinal chemistry