Kinetics Study of the Formation of Pyrmidine Thione from the Reaction of 2,6-Dibenzylidinecyclohexanone and its Derivatives with Thiourea

Kaka, Kosrat and Dabbagh, Abdulmajeed and Hamad, Wali (2016) Kinetics Study of the Formation of Pyrmidine Thione from the Reaction of 2,6-Dibenzylidinecyclohexanone and its Derivatives with Thiourea. ARO-The Scientific Journal of Koya University, 4 (2). pp. 37-42. ISSN 2307-549X

[img] Text
ARO.10142-VOL4.No2.2016.ISSUE07-pp37-42.pdf - Published Version
Available under License Creative Commons Attribution Non-commercial Share Alike.

Download (776kB)
Official URL: http://dx.doi.org/10.14500/aro.10142

Abstract

Kinetics of the addition of thiourea to 2,6-dibenzylidenecyclohexanone and its derivatives have been studied. The reaction is found as a pseudo-first order process which includes a nucleophilic attack by thiourea at the carbonyl group of the ketone system to produce the heterocyclic pyrimidine thione "thiopyrimidine" (Claisen route mechanism). The effect of the substituents at the para position of the 2,6-dibenzylidenecyclohexanone and its derivatives on the rate of reaction, at different temperatures, is studied. Arrhenius parameters, entropies, enthalpies and free energies of activations are estimated. A suitable mechanism, which is correspondent with the results and with Claisen routes mechanism, is suggested for this reaction.

Item Type: Article
Uncontrolled Keywords: 2,6-dibenzylidenecyclohexanone and its derivatives, mechanism route, kinetics study, thiourea, thiopyrimidine.
Subjects: Q Science > QD Chemistry
Divisions: Aro-The Scientific Journal of Koya University > VOL 4, NO 2 (2016)
Depositing User: Dr Salah Ismaeel Yahya
Date Deposited: 04 Aug 2017 15:03
Last Modified: 07 Aug 2017 06:25
URI: http://eprints.koyauniversity.org/id/eprint/101

Actions (login required)

View Item View Item