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Author Question: How could you change the reaction conditions given to most strongly favor an E1 mechanism? (Read 412 times)

majortom123

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on: Feb 17, 2022

Question 1

How could you change the reaction conditions given to most strongly favor an E2 mechanism?



◦ Increase the concentration of the reactant
◦ Add a stronger nucleophile
◦ Use a tertiary alkyl halide
◦ Use a higher concentration of water
◦ Use a stronger base

Question 2

How could you change the reaction conditions given to most strongly favor an E1 mechanism?



◦ Use a weaker base
◦ Increase the concentration of the reactant
◦ Use a primary alkyl halide
◦ Use a higher concentration of water
◦ Use a stronger nucleophile
Organic Chemistry ¦ Klein ¦ 4th Edition
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Marked as best answer by majortom123 on Feb 17, 2022

studyforce.com

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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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majortom123

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

mjenn52

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Reply 3 on: Yesterday
:D TYSM

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