Page 1 of 1

R-sec-butyl chloride was subjected to potassium cyanide in acetonitrile solution. As expected, one product resulted, S-2

Posted: Mon Jul 11, 2022 1:20 pm
by answerhappygod
R Sec Butyl Chloride Was Subjected To Potassium Cyanide In Acetonitrile Solution As Expected One Product Resulted S 2 1
R Sec Butyl Chloride Was Subjected To Potassium Cyanide In Acetonitrile Solution As Expected One Product Resulted S 2 1 (26.3 KiB) Viewed 42 times
R Sec Butyl Chloride Was Subjected To Potassium Cyanide In Acetonitrile Solution As Expected One Product Resulted S 2 2
R Sec Butyl Chloride Was Subjected To Potassium Cyanide In Acetonitrile Solution As Expected One Product Resulted S 2 2 (24.04 KiB) Viewed 42 times
R-sec-butyl chloride was subjected to potassium cyanide in acetonitrile solution. As expected, one product resulted, S-2-methylbutanenitrile. The SN2 mechanism is very much the case here. Which one of the following is a part of the mechanism of the reaction below? KCN CH3CN CN
O O 6₂ NC: (+) EN: :CEN: