occurs. Select the correct statements about the mechanism in Figure 11. The alkene is formed by an E2 mechanism. H₂O is a stronger base than the bromide ion. The reaction proceeds through a relatively stable 3° carbocation. The first elementary step should take place faster than the second elementary step. The proposed mechanism plausible when considering the reagent and reaction conditions. Figure 11 →ör: CH3-C-CH₂-CH3 CH₂ Ö-H H H ON CH₂-C CH-CH₂ CH3 CH₂ CH₂ H-ÖⓇH H C=CH-CH₂

occurs. Select the correct statements about the mechanism in Figure 11. The alkene is formed by an E2 mechanism. H₂O is a stronger base than the bromide ion. The reaction proceeds through a relatively stable 3° carbocation. The first elementary step should take place faster than the second elementary step. The proposed mechanism plausible when considering the reagent and reaction conditions. Figure 11 →ör: CH3-C-CH₂-CH3 CH₂ Ö-H H H ON CH₂-C CH-CH₂ CH3 CH₂ CH₂ H-ÖⓇH H C=CH-CH₂

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter15: Radical Reactions

Section: Chapter Questions

Problem 12E

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