The kinetics and mechanism of cyclization of the anionic sigma complex obtained from the reaction of 1,3,5-trinitrobenzene (TNB) and 1-benzyl-1-(ethoxycarbonyl)-2-propanone (BEP) in the presence of triethylamine (NEt 3 ) have been studied in CH 3 CN-CH 3 OH (50% v/v). The order of the reaction has been found to be zero in TNB and BEP, unity in NEt 3 , and negative and nonintegral in triethylammonium chloride. The rate has been observed to increase slightly
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