A Mechanistic Study on Alkaline Hydrolysis of Y-Substituted Phenyl Benzenesulfonates

Bulletin of the Korean chemical society

Li Ra Im¹  Ik Hwan Um¹  Youn Min Park¹ 

关键词: Alkaline hydrolysis;    Rate-determining step;    Concerted mechanism;    Transition state;    Yukawa-Tsuno equation;   

DOI  :  

学科分类：化学（综合）

来源: Korean Chemical Society

【 摘 要 】

Second-order rate constants (k_OH-) have been measured spectrophotometrically for reactions of Y-substituted phenyl benzenesulfonates (1a-h) with OH? in H2O containing 20 mol % DMSO at 25.0 �? 0.1 oC. The Br┆nstedtype plot is linear with �?_lg = ?0.55 including the points for the reactions of 2,4-dinitrophenyl benzenesulfonate (1a) and 4-chloro-2-nitrophenyl benzenesulfonate (1c), indicating that the ortho-nitro group on the leaving aryloxide does not exert steric hindrance in the current reactions. The Hammett plot correlated with ヲo constants exhibits highly scattered points, while the Hammett correlation with �?? constants results in a slightly better correlation but still many points deviate from the linearity. In contrast, the Yukawa-Tsuno plot shows an excellent linear correlation with r = 0.52, implying that leaving-group departure occurs at the RDS either in a stepwise mechanism or in a concerted pathway. However, the stepwise mechanism in which the leaving group departs in the RDS is excluded since the incoming OH? is much more basic and a poorer nucleofuge than the leaving aryloxide. Thus, the alkaline hydrolysis of 1a-h has been concluded to proceed through a concerted mechanism.

【 授权许可】

Unknown