which of following alcohols can be oxidized to be a carboxylic acid. Name the carboxylic acid produced. Those that cannot be oxidized to a carboxylic acid name the final product
A. ethanol
b. 2-propanol
c. 1-propanol
d. 3-pentanol
2 answers
A and C can be oxidized to form carboxylic acids, and the rest of them will form ketones.
Why are we deprotonating the carboxylic acid that is initially dissolved in the dichloromethane?
By deprotonating the carboxylic acid, it becomes soluble in the aqueous HCl extracting layer.
By deprotonating the carboxylic acid, it becomes soluble in the aqueous NaOH extracting layer.
There is no deprotonation taking place. The carboxylic acid is simply more soluble in the extracting HCl layer.
There is no deprotonation taking place. The carboxylic acid is simply more soluble in the extracting NaOH layer.
By deprotonating the carboxylic acid, it becomes soluble in the aqueous HCl extracting layer.
By deprotonating the carboxylic acid, it becomes soluble in the aqueous NaOH extracting layer.
There is no deprotonation taking place. The carboxylic acid is simply more soluble in the extracting HCl layer.
There is no deprotonation taking place. The carboxylic acid is simply more soluble in the extracting NaOH layer.
1 answer