<?xml version="1.0"?>
<records>
  <record>
    <language>eng</language>
    <publisher>Ansari Education and Research Society</publisher>
    <journalTitle>Journal of Ultra Chemistry</journalTitle>
    <issn>0973-3450</issn>
    <eissn>2319-8036</eissn>
    <publicationDate>June 2006</publicationDate>
    <volume>2</volume>
    <issue>2</issue>
    <startPage>91</startPage>
    <endPage>98</endPage>
    <doi>juc</doi>
    <publisherRecordId>811</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Kinetics and mechanism of Ru(III) catalysed oxidation of m-hydroxy benzoic acid by sodium N-bromobenzenesulphonamide in perchloric acid medium</title>
    <authors>
      <author>
        <name>R.A. Singh (rsinghtdc@rediffmail.com)</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Jyoti Verma</name>
        <affiliationId>2</affiliationId>
      </author>
      <author>
        <name>V.K. Srivastava</name>
        <affiliationId>2</affiliationId>
      </author>
      <author>
        <name> V.K. Shukla</name>
        <affiliationId>2</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Chemistry, T.D. College, Jaunpur (U.P.) INDIA</affiliationName>
      <affiliationName affiliationId="2">Department of Chemistry, T.D.P.G., College, Jaunpur, (V.B.S.) Purvachal Universtiy, Jaunpur (U.P.) 222002 (INDIA)</affiliationName>
    </affiliationsList>
    <abstract language="eng">&lt;p&gt;&lt;br /&gt;&#xD;
Kinetic studies of the oxidation of m-hydroxy benzoic acid(m-HBA) by sodium N-bromobenzenesulphonamide (Bromamine-B or BAB) has heen carried out in aqueous HC1O4&amp;nbsp;medium at (308&amp;plusmn;0.1K). The reaction shows first order dependence each on [BAB], [m-HBA] and catalyst [Ru(III)]. During the reaction, it is observed that there is an inverse first order with respect to [H+]. The rate remained unchanged with the variation in the ionic strength of the medium for [m-HBA]. The addition of benzene sulphonamide [BSA], which is one of the reaction products, had no significant effect on the reaction rate. Thermodynamic parameters were computed by studying the reaction at different temperatures (303&amp;plusmn;318K). The rate laws derived are in excellent agreement with the experimental results. A suitable mechanism has been proposed.&lt;br /&gt;&#xD;
&lt;em&gt;Key words :&lt;/em&gt; m-hydroxy benzoic acid, N-Bromobenzene sulphonamide, Ru(IIl), Perchloric acid, Kinetics and Mechanism.&lt;/p&gt;&#xD;
</abstract>
    <fullTextUrl format="html">https://journalofchemistry.org/paper/811/</fullTextUrl>
    <keywords>
      <keyword language="eng">Kinetics and Mechanism</keyword>
    </keywords>
    <keywords>
      <keyword language="eng">Perchloric acid</keyword>
    </keywords>
  </record>
</records>
