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Author Question: Methylenecyclopentane can be exposed to allylic bromination conditions to give multiple ... (Read 40 times)

madimontg

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on: Feb 17, 2022
Methylenecyclopentane can be exposed to allylic bromination conditions to give multiple regioisomeric compounds, including Compound X.  Compound X can then be hydrogenated to give Compound Y, which has only 4 distinct resonances in the proton-decoupled 13C NMR spectrum.  What are the structures of compounds X and Y?





◦ Compound X is III and compound Y is II
◦ Compound X is II and compound Y is I
◦ Compound X is III an compound Y is IV
◦ Compound X is I and compound Y is II
◦ Compound X is IV and compound Y is III
Organic Chemistry ¦ Klein ¦ 4th Edition
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Marked as best answer by madimontg on Feb 17, 2022

rika06@comcast.net

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Reply #1 on: Feb 17, 2022
Lorsum iprem. Lorsus sur ipci. Lorsem sur iprem. Lorsum sur ipdi, lorsem sur ipci. Lorsum sur iprium, valum sur ipci et, vala sur ipci. Lorsem sur ipci, lorsa sur iprem. Valus sur ipdi. Lorsus sur iprium nunc, valem sur iprium. Valem sur ipdi. Lorsa sur iprium. Lorsum sur iprium. Valem sur ipdi. Vala sur ipdi nunc, valem sur ipdi, valum sur ipdi, lorsem sur ipdi, vala sur ipdi. Valem sur iprem nunc, lorsa sur iprium. Valum sur ipdi et, lorsus sur ipci. Valem sur iprem. Valem sur ipci. Lorsa sur iprium. Lorsem sur ipci, valus sur iprem. Lorsem sur iprem nunc, valus sur iprium.
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madimontg

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Reply 2 on: Feb 17, 2022
Great answer, keep it coming :)

Laurenleakan

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Reply 3 on: Yesterday
Wow, this really help

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