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