Sugars containing either aldehyde (aldose), ketone (ketose) or hemiacetal groups can be oxidized and are classified as reducing sugars. As oxidation of carbohydrates is widely studied under the field of organic chemistry, the present work deals with the study of the redox reactions between peroxodisulphate and xylose underuncatalyzed and catalyzed conditions. The kinetic study of the above reactions showed that these reactions followed first order with respect to peroxodisulphate and the silver nitrate ion catalyst and a fractional order of (0.2) with respect to xylose. Ag catalyst was used to increase the rate of reaction in case of xylose where reactions proceed very slowly with respect to time as compared to other sugars used. The oxidation showed that configuration of sugars has some bearing on rate of oxidation. At lower concentration of oxidants, the linear dependence of reaction rate tends towards new order at their higher concentration. The rate of reaction was affected at elevated temperature where thermodynamic activation parameters like activation energy (Ea), enthalpy change of activation (∆H#), free energy change of activation (∆G#) and entropy change of activation (∆S#) were determined by Arrhenius and Erying equations. The analysis of the reaction products using IR revealed the presence of formaldehyde and formic acid. A mechanism of the reactions was proposed to explain the experimentally observed rate law and the products.
Published in | American Journal of Quantum Chemistry and Molecular Spectroscopy (Volume 4, Issue 1) |
DOI | 10.11648/j.ajqcms.20200401.11 |
Page(s) | 1-6 |
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Oxidation, Kinetic, Xylose, Peroxodisulphate
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APA Style
Mawia Hassan Elsaim, Jubrallah Elhaj, Ibrahim Mukhtar. (2020). Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate. American Journal of Quantum Chemistry and Molecular Spectroscopy, 4(1), 1-6. https://doi.org/10.11648/j.ajqcms.20200401.11
ACS Style
Mawia Hassan Elsaim; Jubrallah Elhaj; Ibrahim Mukhtar. Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate. Am. J. Quantum Chem. Mol. Spectrosc. 2020, 4(1), 1-6. doi: 10.11648/j.ajqcms.20200401.11
@article{10.11648/j.ajqcms.20200401.11, author = {Mawia Hassan Elsaim and Jubrallah Elhaj and Ibrahim Mukhtar}, title = {Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate}, journal = {American Journal of Quantum Chemistry and Molecular Spectroscopy}, volume = {4}, number = {1}, pages = {1-6}, doi = {10.11648/j.ajqcms.20200401.11}, url = {https://doi.org/10.11648/j.ajqcms.20200401.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajqcms.20200401.11}, abstract = {Sugars containing either aldehyde (aldose), ketone (ketose) or hemiacetal groups can be oxidized and are classified as reducing sugars. As oxidation of carbohydrates is widely studied under the field of organic chemistry, the present work deals with the study of the redox reactions between peroxodisulphate and xylose underuncatalyzed and catalyzed conditions. The kinetic study of the above reactions showed that these reactions followed first order with respect to peroxodisulphate and the silver nitrate ion catalyst and a fractional order of (0.2) with respect to xylose. Ag catalyst was used to increase the rate of reaction in case of xylose where reactions proceed very slowly with respect to time as compared to other sugars used. The oxidation showed that configuration of sugars has some bearing on rate of oxidation. At lower concentration of oxidants, the linear dependence of reaction rate tends towards new order at their higher concentration. The rate of reaction was affected at elevated temperature where thermodynamic activation parameters like activation energy (Ea), enthalpy change of activation (∆H#), free energy change of activation (∆G#) and entropy change of activation (∆S#) were determined by Arrhenius and Erying equations. The analysis of the reaction products using IR revealed the presence of formaldehyde and formic acid. A mechanism of the reactions was proposed to explain the experimentally observed rate law and the products.}, year = {2020} }
TY - JOUR T1 - Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate AU - Mawia Hassan Elsaim AU - Jubrallah Elhaj AU - Ibrahim Mukhtar Y1 - 2020/07/06 PY - 2020 N1 - https://doi.org/10.11648/j.ajqcms.20200401.11 DO - 10.11648/j.ajqcms.20200401.11 T2 - American Journal of Quantum Chemistry and Molecular Spectroscopy JF - American Journal of Quantum Chemistry and Molecular Spectroscopy JO - American Journal of Quantum Chemistry and Molecular Spectroscopy SP - 1 EP - 6 PB - Science Publishing Group SN - 2994-7308 UR - https://doi.org/10.11648/j.ajqcms.20200401.11 AB - Sugars containing either aldehyde (aldose), ketone (ketose) or hemiacetal groups can be oxidized and are classified as reducing sugars. As oxidation of carbohydrates is widely studied under the field of organic chemistry, the present work deals with the study of the redox reactions between peroxodisulphate and xylose underuncatalyzed and catalyzed conditions. The kinetic study of the above reactions showed that these reactions followed first order with respect to peroxodisulphate and the silver nitrate ion catalyst and a fractional order of (0.2) with respect to xylose. Ag catalyst was used to increase the rate of reaction in case of xylose where reactions proceed very slowly with respect to time as compared to other sugars used. The oxidation showed that configuration of sugars has some bearing on rate of oxidation. At lower concentration of oxidants, the linear dependence of reaction rate tends towards new order at their higher concentration. The rate of reaction was affected at elevated temperature where thermodynamic activation parameters like activation energy (Ea), enthalpy change of activation (∆H#), free energy change of activation (∆G#) and entropy change of activation (∆S#) were determined by Arrhenius and Erying equations. The analysis of the reaction products using IR revealed the presence of formaldehyde and formic acid. A mechanism of the reactions was proposed to explain the experimentally observed rate law and the products. VL - 4 IS - 1 ER -