THE POLAROGRAPHY OF THE MONOXIMES AND DIOXIMES OF BENZOQUINONE, NAPHTHOQUINONE, AND ANTHRAQUINONE
- 1 January 1956
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 34 (1), 4-13
- https://doi.org/10.1139/v56-002
Abstract
The polarographic behavior of the monoximes and dioximes of 1,4-benzoquinone, 1,4-naphthoquinone, 1,2-naphthoquinone, and 9,10-anthraquinone has been investigated in the pH range 3 to 14. All of the compounds produce well-defined polarographic reduction waves which can be used for analytical purposes. Polarographic evidence indicates that the monoximes and the dioximes exhibit tautomerism.Keywords
This publication has 7 references indexed in Scilit:
- Polarographic reduction of aromatic nitrocompoundsCollection of Czechoslovak Chemical Communications, 1949
- The Polarography of Certain Substances Related to Anthraquinone1Journal of the American Chemical Society, 1948
- Polarographic Behavior of Nitrosophenylhydroxylamine1Journal of the American Chemical Society, 1948
- Conjugated Systems in the Anthracene Series. IV. Transannular Anthranol PeroxidesJournal of the American Chemical Society, 1945
- Polarographic Investigations of Hydrogen Bonding. I. ortho- and para-Nitrophenols1Journal of the American Chemical Society, 1943
- Amperometric Titrations. V. The Titration of Cobalt with α-Nitroso-β-naphtholJournal of the American Chemical Society, 1940
- OXIDATION-REDUCTION POTENTIALS OF A SERIES OF NITROSOBENZENE-PHENYLHYDROXYLAMINE SYSTEMSThe Journal of Organic Chemistry, 1937