Consider the para-substituted aromatic ketones, NO2C6H4COCH3 (p-nitroacetophenone) and CH3OC6H4COCH3 (p-methoxyacetophenone).a. Which carbonyl compound is more stable?b. Which compound forms the higher percentage of hydrate at equilibrium?c. Which compound exhibits a carbonyl absorption at higher wavenumber in its IR spectrum? Explain your reasoning ineach part.
Consider the para-substituted aromatic ketones, NO2C6H4COCH3 (p-nitroacetophenone) and CH3OC6H4COCH3 (p-methoxyacetophenone).a. Which carbonyl compound is more stable?b. Which compound forms the higher percentage of hydrate at equilibrium?c. Which compound exhibits a carbonyl absorption at higher wavenumber in its IR spectrum? Explain your reasoning ineach part.
Chapter19: Reactivities Of Some Alkyl Halides
Section: Chapter Questions
Problem 5Q
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Consider the para-substituted
a. Which carbonyl compound is more stable?
b. Which compound forms the higher percentage of hydrate at equilibrium?
c. Which compound exhibits a carbonyl absorption at higher wavenumber in its IR spectrum? Explain your reasoning in
each part.
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