OHNaOHHalobenzenes that do not have electron-withdrawing groups can still undergo substitution under conditions of high terpressure. The reaction proceeds via a triple-bond intermediate called benzyne, Normal triple bonds arise from the overp orbitals to form two pi bonds. In benzyne, the first pi bond is formed normally, but the second is formed via weak oorbitals.Draw curved arrows to show the movement of electrons in this step of the mechanism.

The above-given reaction is SN2 Substitution reaction taking place on the benzene. The reaction…

CI NaOH Halobenzenes that do not have electron-withdrawing groups can still undergo substitution under conditions of high pressure. The reaction proceeds via a triple-bond intermediate called benzyne. Normal triple bonds arise from the ov p orbitals to form two pi bonds. In benzyne, the first pi bond is formed normally, but the second is formed via weak orbitals Draw curved arrows to showw the movement of electrons in this step of the mechanism.

CI NaOH Halobenzenes that do not have electron-withdrawing groups can still undergo substitution under conditions of high pressure. The reaction proceeds via a triple-bond intermediate called benzyne. Normal triple bonds arise from the ov p orbitals to form two pi bonds. In benzyne, the first pi bond is formed normally, but the second is formed via weak orbitals Draw curved arrows to showw the movement of electrons in this step of the mechanism.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section19.9: Crossed Enolate Reactions Using Lda

Problem JQ

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