Answered

Welcome to Westonci.ca, where finding answers to your questions is made simple by our community of experts. Get precise and detailed answers to your questions from a knowledgeable community of experts on our Q&A platform. Get precise and detailed answers to your questions from a knowledgeable community of experts on our Q&A platform.

When Ethyl Acetoacetate is treated with 1,3-Dibromopropane and 2 moles of Sodium Ethoxide in Ethanol, a compound is produced that has the formula C9H14O3. This compound has an infrared spectrum that shows only one carbonyl adsorption and no OH bond stretch. Suggest a structure for this compound, and provide a mechanism for its formation.

Sagot :

Answer:

The reaction of ethyl acetoacetate with 1,3-Dibromopropane and 2 moles of Sodium Ethoxide in Ethanol.

Explanation:

The structure of ethyl acetoacetate is shown below:

The structure of 1,3-dibromopropane is shown below:

Ethyl acetoacetate on reaction with sodium ethoxide in ethanol forms a carbanion intermediate and the formation of carbanion takes place twice and form a cyclic ring.

The entire reaction is shown below:

The structure of C9H14O3 is shown in the chemical reaction that is shown below:

View image almatheia
View image almatheia
View image almatheia
We hope this information was helpful. Feel free to return anytime for more answers to your questions and concerns. Thank you for visiting. Our goal is to provide the most accurate answers for all your informational needs. Come back soon. Get the answers you need at Westonci.ca. Stay informed by returning for our latest expert advice.