The reaction of 2-methylindole with hexacyanoferrate(III) in alkaline media to produce the corresponding 2-methylindolin-3-one has been studied at constant temperature and ionic strength. The reaction followed first order kinetics with respect to [2-methylindole], [OH-] and [Fe(CN)63-]. The effects of added electrolytes, potassium hexacyanoferrate(II), relative permitivity and temperature have also been studied. On the basis of experimental observations, a probable reaction mechanism has been proposed.
Amer, I. (2021). Kinetics and Mechanism of The Oxidation of 2-Methylindole by Alkaline Potassium Hexacyanoferrate(III). Egyptian Journal of Chemistry, 64(3), 1441-1446. doi: 10.21608/ejchem.2020.22459.2338
MLA
Iqab Adel Amer. "Kinetics and Mechanism of The Oxidation of 2-Methylindole by Alkaline Potassium Hexacyanoferrate(III)". Egyptian Journal of Chemistry, 64, 3, 2021, 1441-1446. doi: 10.21608/ejchem.2020.22459.2338
HARVARD
Amer, I. (2021). 'Kinetics and Mechanism of The Oxidation of 2-Methylindole by Alkaline Potassium Hexacyanoferrate(III)', Egyptian Journal of Chemistry, 64(3), pp. 1441-1446. doi: 10.21608/ejchem.2020.22459.2338
VANCOUVER
Amer, I. Kinetics and Mechanism of The Oxidation of 2-Methylindole by Alkaline Potassium Hexacyanoferrate(III). Egyptian Journal of Chemistry, 2021; 64(3): 1441-1446. doi: 10.21608/ejchem.2020.22459.2338
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