what would be seen if you analyzed salicylic acid in FeCl3?
This is a commonly used test to detect the presence of phenolic hydroxyl groups in organic compounds. The reaction between salicylic acid and FeCl3 forms a complex with a purple color, indicating the presence of phenolic groups in the compound.
Salicylic acid, like any other acid, would be dissolved in water.
Salicylic acid is a solid at room temperature.
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.
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 is a commonly used test to detect the presence of phenolic hydroxyl groups in organic compounds. The reaction between salicylic acid and FeCl3 forms a complex with a purple color, indicating the presence of phenolic groups in the compound.
Salicylic acid, like any other acid, would be dissolved in water.
Salicylic acid is a solid at room temperature.
To prepare a 1% salicylic acid ointment that is 15 g in size, you would need 0.15 g of salicylic acid. This is calculated by multiplying 15 g by 0.01 (1%). Therefore, 0.15 g of salicylic acid would be required for the preparation.
My mixture came out light brownish, due to the fact that my aspirin was still moist with water. When it mixes w/ salicylic acid, it's purplish/to black.
You can find Salicylic Acid in a lot of Acne medications.
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.
Salicylic acid is more polar than aspirin because it has a higher solubility in water due to the presence of a hydroxyl group that enhances its polarity. Aspirin, on the other hand, has an ester functional group, which reduces its overall polarity compared to salicylic acid.
When this salicylate dianion is mixed with an acidic solution of FeCl3(aq), iron(III) chloride, a highly colored (VIOLET) iron (III)-salicylate complex is produced. The maximum absorption of the complex is at about 535 nm.
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.
No, salicylic acid is not soluble in citrate solutions. Salicylic acid is an organic compound that is generally insoluble in water-based solutions like citrate.
Salicylic acid is also known as 2-Hydroxybenzoic acid. The literature Ka value is 2x10 to the negative 14th power. Which makes salicylic acid a somewhat strong acid.