Photolysis of 2-methylcyclohexanone

CC Badcock, MJ Perona, GO Pritchard…

Index: Badcock,C.C. et al. Journal of the American Chemical Society, 1969 , vol. 91, p. 543 - 546

Full Text: HTML

Citation Number: 23

Abstract

Abstract: The photolysis of 2-methylcyclohexanone at 3130 A in both the gas and liquid phase has been critically reexamined. Contrary to an earlier report, both trans-and cis-5- heptenal are obtained as major products. Separate photolysis of various mixtures of the product aldehydes established that these geometric isomers are not readily interconverted under the reaction conditions. It can therefore be concluded that the unsaturated ...

Related Articles:

THE ALIPHATIC DIOLEFINS. III. THE BEHAVIOR OF▵-1, 5-HEXADIENE AND▵-2, 4-HEXADIENE TOWARD HYDROCHLORIC ACID

[Cortese Journal of the American Chemical Society, 1930 , vol. 52, p. 1519]

More Articles...