Answered

Welcome to Westonci.ca, where you can find answers to all your questions from a community of experienced professionals. Get quick and reliable solutions to your questions from a community of experienced professionals on our platform. Connect with a community of professionals ready to help you find accurate solutions to your questions quickly and efficiently.

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 appreciate your visit. Hopefully, the answers you found were beneficial. Don't hesitate to come back for more information. Thank you for your visit. We're committed to providing you with the best information available. Return anytime for more. Stay curious and keep coming back to Westonci.ca for answers to all your burning questions.