BAWA, RAMADAN ALI and ALZARAIDE, EBTISAM MOHAMMED (2015) THE FORMATION OF THE HYDRAZONE TAUTOMER IN HIGH RATIO DURING THE SYNTHESIS OF 4-(9-ANTHRYLAZO)-1-NAPHTHOL. Journal of Basic and Applied Research International, 4 (1). pp. 39-42.
Full text not available from this repository.Abstract
A mixture of two tautomers was found to be formed throughout the synthesis of the phenolic azo dye that is consisting of an anthracene moiety. The coupling reaction between the 9-anthryl diazonium bisulphate and the 1-naphthol yielded a 58% of a mixture of the azo phenol tautomer and its hydrazone counterpart. The spectroscopic data from the IR and NMR revealed the existence of these two tautomers. The tautomeric ratio was found to be of (1:4.5).
| Item Type: | Article |
|---|---|
| Subjects: | Archive Paper Guardians > Multidisciplinary |
| Depositing User: | Unnamed user with email support@archive.paperguardians.com |
| Date Deposited: | 12 Dec 2023 04:32 |
| Last Modified: | 12 Dec 2023 04:32 |
| URI: | http://archives.articleproms.com/id/eprint/2502 |
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