The oxidation of 3,3′-dimethoxy benzidine with potassium bromate in acidic solutions
The kinetics and mechanism of the oxidation of 3,3′‐dimethoxybenzidine (oda, o‐dianisidine) by potassium bromate in aqueous acidic medium were studied by monitoring the formation rate of the reaction product, 3,3′‐dimethoxy 4,4′‐diphenoquinone at 447 nm. The reaction is, first order with respect to...
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Veröffentlicht in: | International journal of chemical kinetics 1991-02, Vol.23 (2), p.113-125 |
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container_title | International journal of chemical kinetics |
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creator | Jonnalagadda, S. B. Munkombwe, N. M. Hensman, P. Mushinga, T. |
description | The kinetics and mechanism of the oxidation of 3,3′‐dimethoxybenzidine (oda, o‐dianisidine) by potassium bromate in aqueous acidic medium were studied by monitoring the formation rate of the reaction product, 3,3′‐dimethoxy 4,4′‐diphenoquinone at 447 nm. The reaction is, first order with respect to both the substrate and oxidant, and second order with respect to H+. The oda: bromate stoichiometric ratio is 1:1. Plausible mechanism and rate laws are proposed accounting the experimental findings. Computer simulations were done using the proposed mechanism. |
doi_str_mv | 10.1002/kin.550230203 |
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B. ; Munkombwe, N. M. ; Hensman, P. ; Mushinga, T.</creator><creatorcontrib>Jonnalagadda, S. B. ; Munkombwe, N. M. ; Hensman, P. ; Mushinga, T.</creatorcontrib><description>The kinetics and mechanism of the oxidation of 3,3′‐dimethoxybenzidine (oda, o‐dianisidine) by potassium bromate in aqueous acidic medium were studied by monitoring the formation rate of the reaction product, 3,3′‐dimethoxy 4,4′‐diphenoquinone at 447 nm. The reaction is, first order with respect to both the substrate and oxidant, and second order with respect to H+. The oda: bromate stoichiometric ratio is 1:1. Plausible mechanism and rate laws are proposed accounting the experimental findings. Computer simulations were done using the proposed mechanism.</description><identifier>ISSN: 0538-8066</identifier><identifier>EISSN: 1097-4601</identifier><identifier>DOI: 10.1002/kin.550230203</identifier><identifier>CODEN: IJCKBO</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Chemistry ; Exact sciences and technology ; Kinetics and mechanisms ; Organic chemistry ; Reactivity and mechanisms</subject><ispartof>International journal of chemical kinetics, 1991-02, Vol.23 (2), p.113-125</ispartof><rights>Copyright © 1991 John Wiley & Sons, Inc.</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3513-c07f7a00c4e7b8fd961cfb85b9f914926527783a0f57310b00c702b5bf3365f63</citedby><cites>FETCH-LOGICAL-c3513-c07f7a00c4e7b8fd961cfb85b9f914926527783a0f57310b00c702b5bf3365f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fkin.550230203$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fkin.550230203$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19398710$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jonnalagadda, S. B.</creatorcontrib><creatorcontrib>Munkombwe, N. M.</creatorcontrib><creatorcontrib>Hensman, P.</creatorcontrib><creatorcontrib>Mushinga, T.</creatorcontrib><title>The oxidation of 3,3′-dimethoxy benzidine with potassium bromate in acidic solutions</title><title>International journal of chemical kinetics</title><addtitle>Int. J. Chem. Kinet</addtitle><description>The kinetics and mechanism of the oxidation of 3,3′‐dimethoxybenzidine (oda, o‐dianisidine) by potassium bromate in aqueous acidic medium were studied by monitoring the formation rate of the reaction product, 3,3′‐dimethoxy 4,4′‐diphenoquinone at 447 nm. The reaction is, first order with respect to both the substrate and oxidant, and second order with respect to H+. The oda: bromate stoichiometric ratio is 1:1. Plausible mechanism and rate laws are proposed accounting the experimental findings. Computer simulations were done using the proposed mechanism.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Kinetics and mechanisms</subject><subject>Organic chemistry</subject><subject>Reactivity and mechanisms</subject><issn>0538-8066</issn><issn>1097-4601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNp9kMFOAjEURRujiYgu3XfjzsHXKW2nS0MUUIIsUJZNp9OGCsyQ6RDAld_kJ_klDoGgK1dvc-65LxehawItAhDfzXzeYgxiCjHQE9QgIEXU5kBOUQMYTaIEOD9HFyG8A4CUhDXQ23hqcbHxma58kePCYXpLvz-_oswvbDUtNluc2vzDZz63eO2rKV4WlQ7BrxY4LYuFriz2OdamJgwOxXy184RLdOb0PNirw22i18eHcacXDV66_c79IDKUERoZEE5oANO2Ik1cJjkxLk1YKp0kbRlzFguRUA2OCUogrUkBccpSRylnjtMmivZeUxYhlNapZekXutwqAmo3iqpHUcdRav5mzy91MHruSp0bH35DkspEEKg5sefWfm63_0vVc3_4t-HwkQ-V3RyTupwpLqhgajLs1tlRb8KfpBrRH120ghY</recordid><startdate>199102</startdate><enddate>199102</enddate><creator>Jonnalagadda, S. 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M. ; Hensman, P. ; Mushinga, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3513-c07f7a00c4e7b8fd961cfb85b9f914926527783a0f57310b00c702b5bf3365f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Kinetics and mechanisms</topic><topic>Organic chemistry</topic><topic>Reactivity and mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jonnalagadda, S. B.</creatorcontrib><creatorcontrib>Munkombwe, N. M.</creatorcontrib><creatorcontrib>Hensman, P.</creatorcontrib><creatorcontrib>Mushinga, T.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>International journal of chemical kinetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jonnalagadda, S. B.</au><au>Munkombwe, N. M.</au><au>Hensman, P.</au><au>Mushinga, T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The oxidation of 3,3′-dimethoxy benzidine with potassium bromate in acidic solutions</atitle><jtitle>International journal of chemical kinetics</jtitle><addtitle>Int. J. Chem. Kinet</addtitle><date>1991-02</date><risdate>1991</risdate><volume>23</volume><issue>2</issue><spage>113</spage><epage>125</epage><pages>113-125</pages><issn>0538-8066</issn><eissn>1097-4601</eissn><coden>IJCKBO</coden><abstract>The kinetics and mechanism of the oxidation of 3,3′‐dimethoxybenzidine (oda, o‐dianisidine) by potassium bromate in aqueous acidic medium were studied by monitoring the formation rate of the reaction product, 3,3′‐dimethoxy 4,4′‐diphenoquinone at 447 nm. The reaction is, first order with respect to both the substrate and oxidant, and second order with respect to H+. The oda: bromate stoichiometric ratio is 1:1. Plausible mechanism and rate laws are proposed accounting the experimental findings. Computer simulations were done using the proposed mechanism.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/kin.550230203</doi><tpages>13</tpages></addata></record> |
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subjects | Chemistry Exact sciences and technology Kinetics and mechanisms Organic chemistry Reactivity and mechanisms |
title | The oxidation of 3,3′-dimethoxy benzidine with potassium bromate in acidic solutions |
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