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Compounds X has the formala CyH15CI: Y is CH15Br. X undergoes base-promoted E2 elimination to give a single alkene product Z. Y likewise reacts under similar conditions to give a single alkene product that is isomerie with Z Catalytic hydrogenation of Z affords 3-ethylpeatane. X readily reacts in S2 fashion with sodium iodide in acetone. Y does not undergo a similar Sy2 reaction. Propose structures for X and Y.

Compounds X has the formala CyH15CI: Y is CH15Br. X undergoes base-promoted E2 elimination to give a single alkene product Z. Y likewise reacts under similar conditions to give a single alkene product that is isomerie with Z Catalytic hydrogenation of Z affords 3-ethylpeatane. X readily reacts in S2 fashion with sodium iodide in acetone. Y does not undergo a similar Sy2 reaction. Propose structures for X and Y.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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o chem - please break down as much as possible, I have no idea how to even begin to figure this out

Compounds X has the formmla C;H13CI: Y is C;H13B1. X undergoes base-promoted E2 elimination to give a single alkene product Z. Y likewise reacts under similar conditions to give a single alkene product that is isomeric with Z Catalytic hydrogenation of Z affords 3-ethylpentane. X readily reacts in Sy2 fashion with sodium iodide in acetone. Y does not undergo a similar Sy2 reaction. Propose structures for X and Y. • Do not use stereobonds in your answer. • In cases where there is more than one possible structure for each molecule, just give one for each. • Draw one structure per sketcher. Add additional sketehers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down mentu.
Transcribed Image Text:Compounds X has the formmla C;H13CI: Y is C;H13B1. X undergoes base-promoted E2 elimination to give a single alkene product Z. Y likewise reacts under similar conditions to give a single alkene product that is isomeric with Z Catalytic hydrogenation of Z affords 3-ethylpentane. X readily reacts in Sy2 fashion with sodium iodide in acetone. Y does not undergo a similar Sy2 reaction. Propose structures for X and Y. • Do not use stereobonds in your answer. • In cases where there is more than one possible structure for each molecule, just give one for each. • Draw one structure per sketcher. Add additional sketehers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down mentu.
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