The kinetics of oxidation of ketones by thallium (III) has been studied in acid perchlorate medium. The reaction does not indicate enolization to be the rate controlling step in the reaction mechanism. The kinetic rate law (1) has been observed. -d[TlIII] / dt= k1Kh [Tl(III)Ketone] / ([H+] + Kh) Where Kh is the hydrolysis constant of the oxidant. A plausible reaction mechanism is suggested conforming to the rate law (1). Activation parameters were evaluated.
Published in | American Journal of Physical Chemistry (Volume 2, Issue 5) |
DOI | 10.11648/j.ajpc.20130205.11 |
Page(s) | 73-79 |
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Kinetics, Mechanism, Oxidation, Butanone, Cyclohexanone, Thallium (III)
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APA Style
Shalini Hemkar, Riya Sailani, Chandra Lata Khandelwal, Prem Dutt Sharma. (2013). Kinetics and Mechanism of Electron-Transfer Reactions: Oxidation of Butanone and Cyclohexanone by Thallium (III) in Acid Perchlorate Medium- An Appraisal of Keto Form Reactivity. American Journal of Physical Chemistry, 2(5), 73-79. https://doi.org/10.11648/j.ajpc.20130205.11
ACS Style
Shalini Hemkar; Riya Sailani; Chandra Lata Khandelwal; Prem Dutt Sharma. Kinetics and Mechanism of Electron-Transfer Reactions: Oxidation of Butanone and Cyclohexanone by Thallium (III) in Acid Perchlorate Medium- An Appraisal of Keto Form Reactivity. Am. J. Phys. Chem. 2013, 2(5), 73-79. doi: 10.11648/j.ajpc.20130205.11
AMA Style
Shalini Hemkar, Riya Sailani, Chandra Lata Khandelwal, Prem Dutt Sharma. Kinetics and Mechanism of Electron-Transfer Reactions: Oxidation of Butanone and Cyclohexanone by Thallium (III) in Acid Perchlorate Medium- An Appraisal of Keto Form Reactivity. Am J Phys Chem. 2013;2(5):73-79. doi: 10.11648/j.ajpc.20130205.11
@article{10.11648/j.ajpc.20130205.11, author = {Shalini Hemkar and Riya Sailani and Chandra Lata Khandelwal and Prem Dutt Sharma}, title = {Kinetics and Mechanism of Electron-Transfer Reactions: Oxidation of Butanone and Cyclohexanone by Thallium (III) in Acid Perchlorate Medium- An Appraisal of Keto Form Reactivity}, journal = {American Journal of Physical Chemistry}, volume = {2}, number = {5}, pages = {73-79}, doi = {10.11648/j.ajpc.20130205.11}, url = {https://doi.org/10.11648/j.ajpc.20130205.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajpc.20130205.11}, abstract = {The kinetics of oxidation of ketones by thallium (III) has been studied in acid perchlorate medium. The reaction does not indicate enolization to be the rate controlling step in the reaction mechanism. The kinetic rate law (1) has been observed. -d[TlIII] / dt= k1Kh [Tl(III)Ketone] / ([H+] + Kh) Where Kh is the hydrolysis constant of the oxidant. A plausible reaction mechanism is suggested conforming to the rate law (1). Activation parameters were evaluated.}, year = {2013} }
TY - JOUR T1 - Kinetics and Mechanism of Electron-Transfer Reactions: Oxidation of Butanone and Cyclohexanone by Thallium (III) in Acid Perchlorate Medium- An Appraisal of Keto Form Reactivity AU - Shalini Hemkar AU - Riya Sailani AU - Chandra Lata Khandelwal AU - Prem Dutt Sharma Y1 - 2013/09/10 PY - 2013 N1 - https://doi.org/10.11648/j.ajpc.20130205.11 DO - 10.11648/j.ajpc.20130205.11 T2 - American Journal of Physical Chemistry JF - American Journal of Physical Chemistry JO - American Journal of Physical Chemistry SP - 73 EP - 79 PB - Science Publishing Group SN - 2327-2449 UR - https://doi.org/10.11648/j.ajpc.20130205.11 AB - The kinetics of oxidation of ketones by thallium (III) has been studied in acid perchlorate medium. The reaction does not indicate enolization to be the rate controlling step in the reaction mechanism. The kinetic rate law (1) has been observed. -d[TlIII] / dt= k1Kh [Tl(III)Ketone] / ([H+] + Kh) Where Kh is the hydrolysis constant of the oxidant. A plausible reaction mechanism is suggested conforming to the rate law (1). Activation parameters were evaluated. VL - 2 IS - 5 ER -