Draw the structure of the organic product formed when the following compounds undergo the…
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Question “Draw the structure of the organic product formed when the following compounds undergo the…”
Draw the structure of the organic product formed when the following compounds undergo the three-step reaction sequence indicated.
Answer
Ethyl Acetoacetate reacts with 1-bromocyclohexane. The product must be given. The base will remove a proton form ethyl Acetoacetate. The base will then attack the alkyl-halide, and in the next step eliminate carbon dioxide.
Due to the presence $math_tag_0 electron-removing groups, the methylene moiety in ethyl Acetoacetate is extremely acidic.
The sodium salt is then formed by reacting with haloalkanes, forming the alkyl derivatives.
Reaction of alkyl derivatives and sodium hydroxide results in a sodium salt derivative. The final product is obtained by heating it in acidic media to release carbon dioxide.
Here is the sodium salt equivalent to ethyl Acetoacetate:
This is the monoalkyl derivative:
This is the final product:
Ans:
The result of the above reaction is:
Conclusion
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