**Question:**Identify the base which is most likely to give Hofmann elimination to the less substituted alkene.**Diagram Explanation:**The diagram presents three different chemical structures labeled I, II, and III, representing potential bases for a Hofmann elimination reaction.- **Structure I:** Sodium ethoxide (Na⁺ C₂H₅O⁻)- **Structure II:** Sodium amide (Na⁺ HN⁻CH₃)- **Structure III:** 1,5-Diazabicyclo[4.3.0]non-5-ene (DBN), a bicyclic amidineThese structures are presented in a box format to indicate they are options for a multiple-choice question.**Answer Choices:**A) I B) II C) III The base that typically leads to Hofmann elimination, favoring the formation of the less substituted alkene, is usually a sterically hindered strong base. Therefore, you would consider factors such as size and basicity when selecting the appropriate base for the reaction.

(I) and (II) both are smaller stronger base so that it's abstract H+ ion from most Sterically…

Answered: Identify the base which is most likely…

Identify the base which is most likely to give Hofmann elimination to the less substituted alkene. II CH3 Na HN Na A) I II .N. B) I| C) II

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter15: Carboxylic Acids And Esters

Section: Chapter Questions

Problem 15.53E: Complete the following reactions: a. b.

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