Identyfikatory
Warianty tytułu
Języki publikacji
Abstrakty
The kinetics of oxidation of amino acids namely, alanine, glycine, leucine, phenyl alanine and valine by N-chloropyrazinamide (NCPZA) in aqueous acetic acid medium in the presence of hydrochloric acid have been investigated. The observed rate of oxidation is first order in [NCPZA], [H+] and [Clˉ]. The order with respect to [amino acid] is zero. The rate of oxidation increases with increase in the percentage of acetic acid. The reaction rate increases slightly with increase in ionic strength, while retards with addition of pyrazinamide. Arrhenius and thermodynamic activation parameters have been evaluated from Arrhenius plot by studying the reaction at different temperatures. A most probable reaction mechanism has been proposed and an appropriate rate law is deduced to account for the observed kinetic data.
Słowa kluczowe
Rocznik
Tom
Strony
1--8
Opis fizyczny
Bibliogr. 26 poz., tab., rys.
Twórcy
autor
- M. A. M. College of Engineering and Technology, Siruganur, Tiruchirappalli - 621 105, Tamil Nadu, India.
autor
- Jayaram College of Engineering and Technology, Karattampatti - Pagalavadi, Thuraiyur (Tk), Tiruchirappalli - 621 014, Tamil Nadu, India.
Bibliografia
- [1] Amauri F. Patrocino, Paulo J. S. Moran, J. Organomet. Chem. 603 (2000) 220-224.
- [2] Sameer P. Dhuru, Nikhil U. Mohe, Manikrao M. Salunkhe, Synth. Commun. 31(23) (2001) 3653-3657.
- [3] V. Canibano, J. F. Rodriguez, M. Santose, M. A. Sanz-Tejedor, M. C. Carreno, G. Gonzalez, J. L. Garcia-Ruano, Synthesis 14 (2001) 2175-2179.
- [4] B. P. Bandgar, L. S. Uppalla, V. S. Sadavarte, Syn. Lett. 11 (2001) 1715-1718.
- [5] Duraisamy Thenraja, Perumal Subramaniam, Chockalingam Srinivasan, J. Chem. Soc. Perkin Trans. 2 (2002) 2125-2129.
- [6] Teruaki Mukaiyama, Jun-ichi Matsuo, Daisuke Lida, Hideo Kitagawa, Chem. Lett. 8 (2001) 846-847.
- [7] N. M. I. Alhaji, S. Sofiya Lawrence Mary, E-J Chem. 8(4) (2011) 1728.
- [8] Ashok Kumar Singh, Rajesh Kumar Singh, Jaya Srivastava, Shahla Rahmani, Sarita Yadav, Indian J. Chem. 51A (2012) 681-689.
- [9] Hemmige S. Yathirajan, Chapuradoddi R. Raju, Kikkeri N. Mohana, Sheena Shashikanth, Padmarajaiah Nagaraja, Turk. J. Chem. 27 (2003) 571-580.
- [10] N. M. I. Alhaji, S. Sofiya Lawrence Mary, E-J Chem. 8(4) (2011) 1472-1477.
- [11] L. Pushpalatha, K. Vivekanandan, J. Indian Chem. Soc. 86(5) (2009) 475-480.
- [12] L. Pushpalatha, K. Vivekanandan, J. Indian Chem. Soc. 85 (2008) 1027-1031
- [13] N. A. Mohamed Farook, R. Prabaharan, S. Rahini, R. Senthil Kumar, G. Rajamahendran, B. Gopala Krishnan, E-J Chem. 1(2), (2004) 127-131.
- [14] Puttaswamy, Nirmala Vaz, Proc. Indian Acad. Sci. (Chem. Sci.) 113(4) (2001) 325-332.
- [15] D. S. Mahadevappa, M. Sayeed Ahamed, N. M. Made Gowda, B. Thimme Gowda, Int. J. Chem. Kinet. 15(8) (1983) 775-793.
- [16] D. S. Mahadevappa, K. S. Rangappa, N. M. Made Gowda, B. Thimme Gowda, Int. J. Chem. Kinet. 14(11) (1982) 1183-1197.
- [17] Y. R. Katre, S. K. Solanki, Sangeeta Patil, Ghanat K. Joshi, Asian J. Chem. 17(1) (2005) 423-428.
- [18] D. S. Mahadevappa, Puttaswamy, N. M. Made Gowda, Proc. Indian Acad. Sci. (Chem. Sci.) 100(4) (1988) 261-274.
- [19] M. Puttaswamy, N. Nirmala Vaz, J. Indian Chem. Soc. 81(6) (2004) 479-483.
- [20] Mangi Lal Bishnoi, Kalyan K. Banerji, Tetrahedron. 41(24) (1985) 6047-6050.
- [21] N. A. Mohamed Farook, G. A. Seyed Dameem, A. Murugesan, M. Kanagaraj, E-J Chem. 1(2) (2004) 132-136.
- [22] A. K. Singh, B. Jain, R. Negi, Y. Katre, S. P. Singh, V. K. Sharma, Synth. React. Inorg. Metal-Org Nano-Metal Chem. 40(2) (2010) 71-77.
- [23] S. Parimala Vaijayanthi, N. Mathiyalagan, Int. J. Res. Org. Chem. 2(3) (2012) 13-15.
- [24] Anjali Lal, M. C. Agrawal, Indian J. Chem. 23A (1984) 411-412.
- [25] K. Vivekanandan, K. Nambi, J. Indian Chem. Soc. 76 (1999) 198-201.
- [26] Musa E. Mohamed, Abdelhafeez M. A. Mohammed, International Letters of Chemistry, Physics and Astronomy 10(1) (2013) 1-17.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-865996fa-cd3c-490b-8e4e-c8adac166f14