Answer the following questions. N N-H Compound 1 Compound 2 Identify which compound is expected to have a lower pkg. Compound 1 O Compound 2 Choose the correct explanation for the above observation. O Compound 1 is not aromatic, but when compound 1 is deprotonated, the resulting conjugate base is aromatic. Therefore, deprotonation of compound 1 results in the formation of aromaticity, which renders compound 1 much more acidic than compound 2 (compound 2 is already aromatic even without being deprotonated). O Compound 1 has more hydrogen atoms and hence it is more acidic than compound 2. O Compound 1 is a five membered ring and hence it is more acidic than compound 2. O Compound 1 has two N-H bonds, so it is more acidic than compound 2, which has only one N-H bond.

Answer the following questions. N N-H Compound 1 Compound 2 Identify which compound is expected to have a lower pkg. Compound 1 O Compound 2 Choose the correct explanation for the above observation. O Compound 1 is not aromatic, but when compound 1 is deprotonated, the resulting conjugate base is aromatic. Therefore, deprotonation of compound 1 results in the formation of aromaticity, which renders compound 1 much more acidic than compound 2 (compound 2 is already aromatic even without being deprotonated). O Compound 1 has more hydrogen atoms and hence it is more acidic than compound 2. O Compound 1 is a five membered ring and hence it is more acidic than compound 2. O Compound 1 has two N-H bonds, so it is more acidic than compound 2, which has only one N-H bond.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 21E

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