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Author Question: Which of the following carbocations is (are) likely to undergo rearrangement through a methide shift? (Read 73 times)

903f23fj0

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on: Feb 17, 2022

Question 1

Which of the molecules below are enantiomers formed as products upon reaction of HBr with 4-methylpent-1-ene?



◦ I and II
◦ II and IV
◦ I and III
◦ II and III
◦ III and IV

Question 2

Which of the following carbocations is (are) likely to undergo rearrangement through a methide shift?



◦ I
◦ II
◦ III
◦ I and II
◦ I, II and III
Organic Chemistry ¦ Klein ¦ 4th Edition
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Marked as best answer by 903f23fj0 on Feb 17, 2022

xinyifff

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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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903f23fj0

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Reply 2 on: Feb 17, 2022
YES! Correct, THANKS for helping me on my review

jomama

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Reply 3 on: Yesterday
Great answer, keep it coming :)

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