Would the following reaction form the product as shown? (CH3CH₂)2NH H A) Yes, it is easier to form the diketone enolate due to the very acidic nature of the methylene hydrogens in between the two carbonyl groups. B) Yes, it is easier to form the aldehyde enolate than the diketone enolate due to the very acidic alpha hydrogens of the aldehyde. C) NO, it is difficult to form the diketone enolate by abstracting the methylene hydrogens due to steric hindrance from the two carbonyl groups. D) NO, it is difficult to form the aldehyde enolate since the alpha hydrogens of the aldehyde are not that acidic. FO O
Would the following reaction form the product as shown? (CH3CH₂)2NH H A) Yes, it is easier to form the diketone enolate due to the very acidic nature of the methylene hydrogens in between the two carbonyl groups. B) Yes, it is easier to form the aldehyde enolate than the diketone enolate due to the very acidic alpha hydrogens of the aldehyde. C) NO, it is difficult to form the diketone enolate by abstracting the methylene hydrogens due to steric hindrance from the two carbonyl groups. D) NO, it is difficult to form the aldehyde enolate since the alpha hydrogens of the aldehyde are not that acidic. FO O
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
Chapter18: Functional Derivatives Of Carboxylic Acids
Section: Chapter Questions
Problem 18.68P: Minoxidil is a molecule that causes hair growth in some people. It was originally synthesized as a...
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