Electron Transfer Reaction of Theobromine and Permanganate Ion in Aqueous Acidic Media

F. Jones, I. Anweting, I. E. Okon
{"title":"Electron Transfer Reaction of Theobromine and Permanganate Ion in Aqueous Acidic Media","authors":"F. Jones, I. Anweting, I. E. Okon","doi":"10.9734/ajacr/2023/v13i2242","DOIUrl":null,"url":null,"abstract":"Electron transfer reaction of theobromine (hereafter referred to as TB) and permanganate ion has been studied using spectrophotometric technique under pseudo first-order conditions at T = 24, [H+] = 3.2 × 10–1 mol dm–3and I = 1.0 mol dm–3 (Na2SO4). Stoichiometric study depicted that two moles of TB were consumed by one mole of permanganate ion. The rate of the reaction is first order in both [TB] and [MnO4-] and second order overall. It was observed that, [H+] and ionic strength respectively enhanced the rate of the reaction in the range studied. Michaelis-Mentens analysis showed no evidence of intermediate complex formation. Added anions and cations were observed to catalyze the reaction rate. The reaction conforms to the rate law as shown below: \n \n -d [MnO4-]/dt = (a+b [H+]) [TB] [MnO4-]                                                                                   \n where a = 0.041 dm3mol–1 s–1 and   b= 0.028 dm3mol–1 s–1.\nThe reaction thus occurs by an outer-sphere pathway and plausible mechanism is proposed for the reaction.","PeriodicalId":8480,"journal":{"name":"Asian Journal of Applied Chemistry Research","volume":"130 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Applied Chemistry Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/ajacr/2023/v13i2242","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Electron transfer reaction of theobromine (hereafter referred to as TB) and permanganate ion has been studied using spectrophotometric technique under pseudo first-order conditions at T = 24, [H+] = 3.2 × 10–1 mol dm–3and I = 1.0 mol dm–3 (Na2SO4). Stoichiometric study depicted that two moles of TB were consumed by one mole of permanganate ion. The rate of the reaction is first order in both [TB] and [MnO4-] and second order overall. It was observed that, [H+] and ionic strength respectively enhanced the rate of the reaction in the range studied. Michaelis-Mentens analysis showed no evidence of intermediate complex formation. Added anions and cations were observed to catalyze the reaction rate. The reaction conforms to the rate law as shown below:     -d [MnO4-]/dt = (a+b [H+]) [TB] [MnO4-]                                                                                     where a = 0.041 dm3mol–1 s–1 and   b= 0.028 dm3mol–1 s–1. The reaction thus occurs by an outer-sphere pathway and plausible mechanism is proposed for the reaction.
可可碱与高锰酸盐离子在酸性水溶液中的电子转移反应
采用分光光度法研究了可可碱(以下简称TB)与高锰酸盐离子在T = 24, [H+] = 3.2 × 10-1 mol dm-3, I = 1.0 mol dm-3 (Na2SO4)的准一级条件下的电子转移反应。化学计量学研究表明,1摩尔高锰酸盐离子能消耗2摩尔TB。[TB]和[MnO4-]的反应速率都是一级反应,总的反应速率是二级反应。在研究范围内,[H+]和离子强度分别提高了反应速率。Michaelis-Mentens分析显示没有中间复杂地层的证据。观察了添加阴离子和阳离子对反应速率的催化作用。反应符合率法如下所示:- d (MnO4 -) / dt = (a + b (H +)) (MnO4(结核病) -]                                                                                     一个= 0.041 dm3mol-1 s - 1和b = 0.028 dm3mol-1 s - 1。因此,该反应是通过外球途径发生的,并提出了合理的反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信