The release of the H+ ion or (the proton) is much easier in the carboxylic acid as the Phenoxide ion is more electron dense than the Carboxy ion. this is because of to the lone pairs of electrons on the oxygen atom delocalising into the benzene pi ring activating the ring and making the phenoxide ion more electron dense make in it harder for it to donate a proton. on the coboxy ion the negative charge is Shared between the two oxygen's making it less electron dense. Making it easier for the carboxylic acid to donate a proton making it a stronger acid.
Both of these are acidic, add ethanol to the solution of both with small amount of sulphuric acid, carboxylic acid forms ester while phenol does not, now add ammonia to solution ester remains liquid while solid salt of phenol precipitated out.
pehol is standard and phenolic is the new agent being tested
Phenol is a much weaker in acidic strength than carboxylic acid with a pKa of 10.00 compared to 4.76 in carboxylic acid.
carboxylic acid is more stable then phenol due to the negative charge is on the more electronegative atom then compound will more stable and acidic
The reaction between Ammonia and a Carboxylic Acid result, counter intuitively, in the production of an Ammonium Carboxylate and not an Amide. This reaction is there for an acid-base neutralization reaction.
Formic acid is methanoic acid. A carboxylic acid.
Picric acid is acidic, as it has a fairly acidic phenolic proton. However, picric acid is not a carboxylic acid. Nevertheless, it is still called 'acid' because of its acidic proton, just as phenol was once called 'carbolic acid'.
A fatty acid salt is a kind of carboxylic acid salt. But not all carboxylic acid salts are fatty acid salts.
what is the reaction between sulphamic acid and phenol
Phenol is converted to aspirin by adding carboxylic acid and esterifying the alcohol.
The difference between a hydrocarbon and a fatty acid is that a fatty acid is a hydrocarbon chain with a carboxylic acid head.
This is actually quite simple: the pKa of the carboxylic acid group is only about 3, but the pKa of the phenolic group is 13.4.
Carboxylic acid.
Esters and amides are derivatives of carboxylic acids. Amines are alkylated derivatives of ammonia: carboxylic acid= R-COOH ester= R-COOR amide=R-CONH2 amine= R-NHR
An alcohol and a carboxylic acid salt (carboxylic acid if protonated at end of reaction).
The reaction between Ammonia and a Carboxylic Acid result, counter intuitively, in the production of an Ammonium Carboxylate and not an Amide. This reaction is there for an acid-base neutralization reaction.
Formic acid is methanoic acid. A carboxylic acid.
Picric acid is acidic, as it has a fairly acidic phenolic proton. However, picric acid is not a carboxylic acid. Nevertheless, it is still called 'acid' because of its acidic proton, just as phenol was once called 'carbolic acid'.
A fatty acid salt is a kind of carboxylic acid salt. But not all carboxylic acid salts are fatty acid salts.
Vinegar is ethanoic acid CH3COOH, so yes it is a carboxylic acid.
what is the reaction between sulphamic acid and phenol