Using orbitals, draw the transition state of the SN2 reaction between sodium cyanide and bromomethane. Which orbitals are interacting with which? Why is the bond breaking? Why is the orientation important? Is there another angle besides backside attack that could theoretically work based on orbital geometry? Why doesn’t this happen?
Using orbitals, draw the transition state of the SN2 reaction between sodium cyanide and bromomethane. Which...
1) State which of the electrophiles given below will react preferentially by i) SN1, ii) by SN2, or iii) capable of reacting by either of the two mechanisms depending on the given conditions. How can you affect those conditions to favour SN1 or SN2? Reason your predictions based on the structures of the compounds. Br-CH3, Br-CH2CH3, Br-CH(CH3)2, Br-C(CH3)3, Br-CH2-C5H6; C5H6 = phenyl 6) Using orbitals, draw the transition state of the SN2 reaction between sodium cyanide and bromomethane. Which orbitals...
1. Which reaction below occurs faster through an SN2 mechanism and why? Draw the transition states of each reaction to explain your answer. OH to bomto Br OH b) OH 2. The reaction of 9.0 g of 1-butanol (MW = 76g/mol) with 13.0 g of sodium bromide (MW = 103 g/mol) with excess acid produces 8.5 g of 1-bromobutane (MW 137 g/mol). a. What is the purpose of the acid? b. What is the % yield for the reaction? Show...