1963Bulletin des Sociétés Chimiques BelgesRequires access

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

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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.

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Available 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.

Key concepts: Cyclopentanone, Cyclohexanone, Cyclobutanone, Chemistry, Exothermic reaction, Entropy (arrow of time), Organic chemistry, Medicinal chemistry

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N.M.R. Experiments on Ketals Part I. Reaction Heat and Entropy of the Methyl Ketal Formation of Cyclohexanone, Cyclopentanone and Cyclobutanone — Research Paper | ScholarLens