✍ Scribed by Marie-Paule Pileni
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FGsb photolysis of NaO saturated neutral aqueous solution of tyroGna phenol and ~cresnl lcads to OH adduct formation. This species subsequently undergoes either unimolecular water elimination to form the phcnoxyl radic,d or bimolecular radical-radical recombination. Alcohol addition to neutral aqueous solutions provokes the formation of hydrogen atom adduct.
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Flash photolysis of 4-diazoisochroman-3-one in aqueous solution resulted in loss of nitrogen and transient production of the a-carbonylcarbene 3-ketoisochroman-4-ylidene, the hydration of which generated a shortlived species that was identified as the enol isomer of the lactone, 4-hydroxyisochroman-
## Abstract The effects of __n__‐hexanol, __n__‐pentanol, and __n__‐butanol on the critical micelle concentration (cmc), on the micellar ionization degree (α), and on the rate of the reaction methyl 4‐nitrobenzenesulfonate + Br^−^ have been investigated in cetyltrimethylammonium bromide (CTAB) aque
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