Kinetics and the mechanism of oxidation of methoxy benzaldehydes by benzimidazolium fluorochromate in an aqueous acetic acid medium

被引:6
作者
Malik, V. Saleem [1 ]
Asghar, Basim H. [2 ]
Mansoor, S. Sheik [1 ]
机构
[1] C Abdul Hakeem Coll Autonomous, Dept Chem, Melvisharam 632509, Tamil Nadu, India
[2] Umm Al Qura Univ, Fac Sci Appl, Dept Chem, POB 9569, Mecca, Saudi Arabia
来源
JOURNAL OF TAIBAH UNIVERSITY FOR SCIENCE | 2016年 / 10卷 / 01期
关键词
Benzimidazolium fluorochromate; Oxidation; Kinetics; Methoxy benzaldehydes; SUBSTITUTED BENZALDEHYDES; CHLOROCHROMATE; ANILINES; ALCOHOLS; REAGENT; MILD;
D O I
10.1016/j.jtusci.2015.05.009
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The oxidation of benzaldehyde (BA) as well as 4-methoxy (4-MBA), 3-methoxy (3-MBA), 2-methoxy (2-MBA), 2,6-dimethoxy (2,6-DMBA), 2,4-dimethoxy (2,4-DMBA), 3,4-dimethoxy (3,4-DMBA), 2,4,6-trimethoxy (2,4,6-TMBA), 3,4,5-trimethoxy (3,4,5TMBA) and 2,3,4-trimethoxy (2,3,4-TMBA) benzaldehydes by benzimidazolium fluorochromate (BIFC) have been studied in a 50% acetic acid-50% water medium. The oxidation leads to the formation of the corresponding carboxylic acids. The reaction is first order with respect to [BIFC], [S] and [H+]. The reaction was catalysed by 1-1 ions. The reaction was studied at four different temperatures, and the thermodynamic parameters were calculated. The Exner plot indicated that all of the methoxy-substituted benzaldehydes were oxidized via the same mechanism. Based on the observed kinetics, a suitable mechanism has been proposed. (C) 2015 The Authors. Production and hosting by Elsevier B.V. on behalf of Taibah University. This is an open access article under the CC BY-NC-ND license (http:/creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:131 / 138
页数:8
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