Question

In each reaction box, place the best reagent and conditions from the list below.

Answer 1

This is a two step step reaction as shown below,

Step 1:
           Epoxidation of Alkene:
                                              In first step Cyclohexene is treated with peroxybenzoic acid in the presence of Dichloromethane which results in the formation of epoxide moiety.

Step 2:
           Nucleophillic Substitution Reaction:
                                                                  In second step the epoxide formed is treated with Sodium Methoxide which acts as a nucleophile and attacks the less hindered carbon of epoxide resulting in the formation of final product as shown below.