Abstract
Defocussed metastable peaks have been used to elucidate the hitherto apparently complex fragmentation of the molecular ion of 1,2-cyclohexanediol. It was shown that the predominant mode of water loss from the molecular ion involved "scrambling" of six hydrogen atoms, those in the 4- and 5-methylene groups and the hydroxyl pair. A minor water elimination involves simple hydroxyl–hydroxyl interaction.

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