What effect would the nonreversible decomposition of acetoacetic acid have on the equilibrium between 3-hydroxybutyric acid and acetoacetic acid? (i.e. which way would if shift?)
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What effect would the nonreversible decomposition of acetoacetic acid have on the equilibrium between 3-hydroxybutyric acid and acetoacetic acid? (i.e. which way would if shift?)
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- Using ChemDraw Draw a mechanism of a reversible reaction of acetophenone and strong acid (H-A) to form a protonated acetophenone and a weak base. Draw all the electron pairs of the molecules and the arrows.5) Imidazole is more basic than pyridine, but more acidic than pyrrole, why? N.Can you please answer what the missing compound A and B are?
- When trichloroacetaldehyde is dissolved in water, almost all of it is converted to the hydrate. Chloral hydrate, the product of the reaction, is a sedative that can be lethal. A cocktail laced with it is known—in detective novels,at least—as a “Mickey Finn.” Explain why an aqueous solution of trichloroacetaldehyde is almost all hydrate.When trichloroacetaldehyde is dissolved in water, almost all of it is converted to the hydrate. Chloral hydrate, the product of the reaction, is a sedative that can be lethal. A cocktail laced with it is known—in detective novels, at least—as a “Mickey Finn.” Explain why an aqueous solution of trichloroacetaldehyde is almost all hydrate.Rank the compounds from most to least acidic
- Why is the N-H bond of an imide especially acidic? A) The conjugate acid is stabilized by resonance. B) The conjugate base is stabilized by resonance. The conjugate base is stabilized by (c) intramolecular hydrogen bonding. The conjugate base is stabilized by electron- (D donating inductive effect.Arrange the molecules and ions in set in order of increasing acidity (from least acidic to most acidic).Explain why using one or two equivalents of NaH results in different products in the following reactions.