Isomerization of Cyclohexyl Phenyl Ketoxirne in Liquid Sulfur Dioxide
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概要
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1. The syn-anti isomerization of β-cyclohexyl phenyl ketoxime is carried out in liquid sulfur dioxide.<BR>2. The isomerization is accerelated by light and retarded by hydroquinone. The degree of the dehydration of liquid sulfur dioxide has little effect on the rate of isomerization.<BR>3. The kinetic result has shown that the reaction is of the first order with respect to the concentration of the oxime and that the rate constant, <I>k</I> for <B>R</B>=<I>k</I>[β-oxime], may be expressed as:<BR><I>k</I>=6.3×10<SUP>11</SUP> exp [−19.1⁄<B>RT</B>]<BR>4. A complex between the oxime and sulfur dioxide is assumed as the intermediate step, the isomerization of the complex being the rate-determining step. The dual (radical and ionic) nature of the isomerization in liquid sulfur dioxide may well be elucidated by such an assumption.
- 社団法人 日本化学会の論文
著者
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TOKURA Niichiro
The Chemical Research Institute of Non-Aqueous Solutions
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Shiina Katsuo
The Chemical Research Institute of Non-Aqueous Solutions Tohoku University
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Tokura N.
The Chemical Research Institute of Non-Aqueous Solutions
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