Aspirin is part of the Mickey Mouse club house in Venezuela. But, a carboxylic acid is part of the Minnie Mouse club house in Brazil.
Neither. Aspirin, acetyl salicylic acid, is a structure containing benzene, carboxylic acid, and ester functional groups, but it does not contain nitrogen at all, let alone eitehr an amine or amide.
Phenol is converted to aspirin by adding carboxylic acid and esterifying the alcohol.
Do not be confused with alcohols nor ketones when seeing the -OH and the =O bonded. They each are really parts of either:- the carboxylic acid group (-COOH)- the ester link (from neighbour carbon along the ring)Likewise, double-bonds you see constitute the benzene (aromatic) ring:- a functional group in itself- they are not the normal alkene double bonds- would actually best be represented by a circle inside the ring,- not double lines for each of 3 double bonds, as resonance occurs in benzene rings.Therefore, aspirin (or acetylsalicylic acid) contains:- aromatic ring- carboxylic acid group- ester groupand can be regarded as an acid (i.e. acetylsalicylic acid)or the acetate ester of salicylic acid :-)so aspirin is (if choosing from your options):- not an alkene, nor a ketone, nor an alcohol.- we are left with a carboxylic acidBUT we usually only regard aspirin as an acetate ester, or a derivative of salicylic acid,so you wouldn't generally hear one calling aspirin a carboxylic acid :-)I hope I cleared things up a bit :-)Cheers.
The carboxylic acid group or -COOH group makes it acidic
The products of a reaction between an ester and water are an alcohol and a carboxylic acid. This reaction is known as hydrolysis and involves the breaking of the ester bond, which results in the formation of the alcohol and carboxylic acid molecules.
Aspirin is acetylsalicylic acid and an acetate ester of salicylic acid.
Salicylic acid is a precursor to aspirin, which is a derivative of salicylic acid. When salicylic acid is acetylated, it becomes aspirin. Aspirin is a common medication used for pain relief and reducing inflammation.
Ester, a carboxylic acid.
Neither. Aspirin, acetyl salicylic acid, is a structure containing benzene, carboxylic acid, and ester functional groups, but it does not contain nitrogen at all, let alone eitehr an amine or amide.
Phenol is converted to aspirin by adding carboxylic acid and esterifying the alcohol.
Do not be confused with alcohols nor ketones when seeing the -OH and the =O bonded. They each are really parts of either:- the carboxylic acid group (-COOH)- the ester link (from neighbour carbon along the ring)Likewise, double-bonds you see constitute the benzene (aromatic) ring:- a functional group in itself- they are not the normal alkene double bonds- would actually best be represented by a circle inside the ring,- not double lines for each of 3 double bonds, as resonance occurs in benzene rings.Therefore, aspirin (or acetylsalicylic acid) contains:- aromatic ring- carboxylic acid group- ester groupand can be regarded as an acid (i.e. acetylsalicylic acid)or the acetate ester of salicylic acid :-)so aspirin is (if choosing from your options):- not an alkene, nor a ketone, nor an alcohol.- we are left with a carboxylic acidBUT we usually only regard aspirin as an acetate ester, or a derivative of salicylic acid,so you wouldn't generally hear one calling aspirin a carboxylic acid :-)I hope I cleared things up a bit :-)Cheers.
The carboxylic acid group or -COOH group makes it acidic
Some examples of drugs that contain carboxylic acids include aspirin (acetylsalicylic acid), ibuprofen, and naproxen. Carboxylic acids are commonly found in medications due to their anti-inflammatory and pain-relieving properties.
No, ch3ch2co2h (also known as ethanoic acid or acetic acid) is not an ester. It is a carboxylic acid. Ester molecules are formed by the reaction between a carboxylic acid and an alcohol.
The reaction between the salt of a carboxylic acid and HCl results in the formation of the carboxylic acid itself and the salt of hydrochloric acid. The general equation for this reaction is: Salt of carboxylic acid + HCl → Carboxylic acid + Salt of hydrochloric acid
The products of a reaction between an ester and water are an alcohol and a carboxylic acid. This reaction is known as hydrolysis and involves the breaking of the ester bond, which results in the formation of the alcohol and carboxylic acid molecules.
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.