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Author Question: We can promote SN2 over SN1 reactions if we: I) use a substrate that gives a primary carbocation and ... (Read 29 times)

Jramos095

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on: Jul 8, 2021

Question 1

The rate of E2 reaction between an alkyl halide RX and a base B is given by the following expression (k is a rate constant):
◦ k[RX]
◦ k[B]
◦ k[RX][B]
◦ k[RX]2
◦ k[RX]2[B]

Question 2

We can promote SN2 over SN1 reactions if we:
I)  use a substrate that gives a primary carbocation and not tertiary carbocation
II)  use a sterically hindered substrate
III)  use a polar protic solvent
◦ I)
◦ II)
◦ III)
◦ I) and III)
◦ II) and III)
General Chemistry: Principles and Modern Applications ¦ Petrucci, Herring, Madura, Bissonnette ¦ 11th Edition
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Marked as best answer by Jramos095 on Jul 8, 2021

voltaire123

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Reply #1 on: Jul 8, 2021
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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Jramos095

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Reply 2 on: Jul 8, 2021
:D TYSM

miss.ashley

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Reply 3 on: Yesterday
Excellent

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