Effect of Position and Number of Hydroxyl Groups on the Oscillatory Behaviour of Isomers of Hydroxybenzoic Acid | Zendy

Masood A. Nath | Zendy; Nadeem Bashir Ganaie | Zendy; R. P. Rastogi | Zendy; Ghulam Mustafa Peerzada | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Open Access

Effect of Position and Number of Hydroxyl Groups on the Oscillatory Behaviour of Isomers of Hydroxybenzoic Acid

Author(s) -

Masood A. Nath,

Nadeem Bashir Ganaie,

R. P. Rastogi,

Ghulam Mustafa Peerzada

Publication year - 2008

Publication title -

journal of chemistry

Language(s) - English

Resource type - Journals

eISSN - 2090-9063

pISSN - 2090-9071

DOI - 10.1155/2009/321340

Subject(s) - bromate , chemistry , halogenation , catalysis , manganese , hydroxybenzoic acid , aqueous solution , ion , medicinal chemistry , stereochemistry , organic chemistry

In the present communication, the effect of isomers of hydroxybenzoic acids with respect to their oscillatory behaviour as organic substrates with inorganic bromate and manganese(II) ion as catalyst in aqueous acid medium (1.0 M H2SO4) have been studied. The number and the relative position of hydroxyl groups (-OH) in the aromatic ring is found to influence the oscillatory behaviour. Besides, the role of bromination reaction and the formation of corresponding bromoderivative is found to be an important step. The experimental findings are within the purview of Field, Koros and Noyes (FKN) mechanism

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research