has a pH of 2
This reaction will not proceed, as the equilibrium is far to the left. In order to synthesize acetylsalicylic acid, one must use acetic anhydrate, and the reaction forms acetic acid instead of water.
The balanced equation for the reaction between salicylic acid and acetic anhydride to form aspirin (acetylsalicylic acid) is: salicylic acid + acetic anhydride → aspirin + acetic acid.
Salicylic acid dissociates in water to form a carboxylic acid group, making it more acidic compared to acetylsalicylic acid which has an ester group that is less acidic. The presence of the -OH group in salicylic acid contributes to its higher acidity compared to the -OR group in acetylsalicylic acid.
The reaction of salicylic acid with acetyl chloride and pyridine results in the formation of acetylsalicylic acid (aspirin). The general equation for this reaction is: salicylic acid + acetyl chloride → acetylsalicylic acid + hydrogen chloride
Salicylic acid acetyl is made by reacting salicylic acid with acetic anhydride in the presence of an acid catalyst, such as sulfuric acid, to form acetylsalicylic acid. This reaction causes the hydroxyl group (-OH) of salicylic acid to be acetylated, resulting in acetylsalicylic acid, commonly known as aspirin.
This reaction will not proceed, as the equilibrium is far to the left. In order to synthesize acetylsalicylic acid, one must use acetic anhydrate, and the reaction forms acetic acid instead of water.
The balanced equation for the reaction between salicylic acid and acetic anhydride to form aspirin (acetylsalicylic acid) is: salicylic acid + acetic anhydride → aspirin + acetic acid.
Salicylic acid dissociates in water to form a carboxylic acid group, making it more acidic compared to acetylsalicylic acid which has an ester group that is less acidic. The presence of the -OH group in salicylic acid contributes to its higher acidity compared to the -OR group in acetylsalicylic acid.
The reaction of salicylic acid with acetyl chloride and pyridine results in the formation of acetylsalicylic acid (aspirin). The general equation for this reaction is: salicylic acid + acetyl chloride → acetylsalicylic acid + hydrogen chloride
Salicylic acid acetyl is made by reacting salicylic acid with acetic anhydride in the presence of an acid catalyst, such as sulfuric acid, to form acetylsalicylic acid. This reaction causes the hydroxyl group (-OH) of salicylic acid to be acetylated, resulting in acetylsalicylic acid, commonly known as aspirin.
The chemical reaction between acetic anhydride and salicylic acid is called esterification. This reaction forms acetylsalicylic acid, which is commonly known as aspirin.
Salicylic acid has a pKa of 1.96 and acetylsalicylic acid (Aspirin) has a pKa of 3.48. Therefore salicylic acid is the stronger acid.
Aspirin is acetylsalicylic acid and an acetate ester of salicylic acid.
ASA (acetylsalicylic acid) or Aspirin is synthesised by reacting Salicylic Acid with Acetic Anhydride. During this esterification, the dehydration occurs on the hydroxyl group attached to the benzene ring. As a result, the product no longer possesses the Phenol functional group.
Aspirin derives its name from its chemical formula, acetylsalicylic acid. The compound is formed from salicylic acid, which is derived from bark from a willow tree. The process was discovered to take away the intense stomach pains associated with salicylic acid.Interesting note: The same mechanism that makes salicylic acid into acetylsalicylic acid also turns morphene into heroin.
With 1,5 g of salicylic acid you can obtain theoretically 1,96 g aspirin (acetylsalicylic acid); but in the laboratory (or industry) I remember that the true yield of reaction is a little more than 90 %.
Salicylic acid is a precursor to aspirin, which is a derivative of salicylic acid. Aspirin is acetylsalicylic acid. They differ in their chemical composition as aspirin has an acetyl group attached to the salicylic acid molecule. In terms of medicinal properties, aspirin is commonly used as a pain reliever, anti-inflammatory, and fever reducer, while salicylic acid is often used in skincare products for its exfoliating properties.