Kinetic Studies on Nucleophilic Substitution Reactions ofO-Aryl Thionobenzoates with Azide, Cyanide, and Hydroxide: Contrasting Reactivity and Mechanism

2009 ◽  
Vol 74 (3) ◽  
pp. 1212-1217 ◽  
Author(s):  
Ik-Hwan Um ◽  
Eun-Hee Kim ◽  
Ji-Youn Lee
1982 ◽  
Vol 60 (19) ◽  
pp. 2500-2520 ◽  
Author(s):  
Kenneth Charles Westaway ◽  
Zbigniew Waszczylo

Kinetic studies, secondary α-deuterium kinetic isotope effects, primary chlorine kinetic isotope effects (1), Hammett ρ values determined by changing the substituent in the nucleophile, and activation parameters have been used to determine the detailed (relative) structures of the transition states for the SN2 reactions between para-substituted benzyl chlorides and thiophenoxide ion. A rationale for the U-shaped Hammett ρ plots observed when para-substituted benzyl compounds react with negatively charged nucleophiles is also presented.


2021 ◽  
Vol 50 (7) ◽  
pp. 2671-2688
Author(s):  
Marina Yu. Stogniy ◽  
Sergey A. Anufriev ◽  
Akim V. Shmal'ko ◽  
Sergey M. Antropov ◽  
Aleksei A. Anisimov ◽  
...  

An unusual reactivity of 9-iodo-nido-carborane [9-I-7,8-C2B9H11]− towards nucleophiles under strong basic conditions was revealed.


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