Complete the curved arrow mechanism of the following double elimination reaction when 1,2-dibromopropane is treated with two equivalents of sodium amide and heated with mineral oil.
Solution :-
In the starting reactant molecule only 3 carbons are present.
Both the Br from the starting are eliminated by using the strong base which results in the formation of the triple bond.
following image shows the correct structure of the product. Rest of the mechanism part is correct.
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