Mechanism of oxidations in partially aqueous media: Kinetics of oxidation of thiosemicarbazide and thiosemicarbazone by chloramine-T and dichloramine-T in aqueous methanol

1989 ◽  
Vol 21 (1) ◽  
pp. 31-50 ◽  
Author(s):  
B. Thimme Gowda ◽  
B. S. Sherigara
Author(s):  
M. Shanmugam Ramachandran ◽  
T. Subburamiyer Vivekanandam ◽  
Rajarathinam Nithyanandhan

1990 ◽  
Vol 55 (6) ◽  
pp. 1535-1540 ◽  
Author(s):  
Prerepa Manikyamba

Kinetics of oxidation of 1- and 2-acetylnaphthalenes by iodate in the presence of sulphuric acid in aqueous methanol has been studied. The reaction is first order with respect to both [iodate] and [acetylnaphthalene]. Solvent effect indicates a cation-dipole type of interaction in the rate limiting step. A mechanism is proposed with a slow attack of IO2+ on enol form of acetylnaphthalene forming an intermediate carbonium ion, which ultimately gives corresponding ω-hydroxyacetylnaphthalene. The higher reactivity of 2-acetyl isomer is attributed to the greater stability of the corresponding carbonium ion than that of 1-acetyl isomer.


2006 ◽  
Vol 59 (10) ◽  
pp. 1157-1165 ◽  
Author(s):  
Ritam Mukherjee ◽  
Basab Bijayi Dhar ◽  
Rupendranath Banerjee ◽  
Subrata Mukhopadhyay

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