Ah, the solubility of salicylic acid in water is quite interesting. You see, salicylic acid is moderately soluble in water, meaning it can dissolve to some extent but not completely. It's like a delicate dance between the water molecules and the salicylic acid particles, finding a balance where they can coexist harmoniously. Just remember, even if it's not completely soluble, a little patience and gentle stirring can help them come together beautifully.
The addition of hydrochloric acid protonates the salicylic acid molecules, converting them into their water-soluble salt form. This increases the solubility of salicylic acid in water as the salt form has greater aqueous solubility due to its ionic nature.
Yes, salicylic acid is slightly soluble in ethanol. However, its solubility in ethanol is much lower compared to its solubility in water.
Salicylic acid does not dissolves very easily in hot and cold water. This acid is widely used in acne medicine. It is derived from the bark of the willow tree.
Salicylic acid is soluble in NaOH and insoluble in NaHCO3 and HCl. In NaOH, salicylic acid can form a salt through neutralization. In NaHCO3 and HCl, salicylic acid remains as a solid due to its low solubility in these solutions.
The precipitate of salicylic acid dissolves in excess sulphuric acid due to the formation of a complex between salicylic acid and sulphuric acid, which increases the solubility of the precipitate. This reaction results in the formation of a colorless solution, as the salicylic acid is converted into its conjugate base form.
The addition of hydrochloric acid protonates the salicylic acid molecules, converting them into their water-soluble salt form. This increases the solubility of salicylic acid in water as the salt form has greater aqueous solubility due to its ionic nature.
Yes, salicylic acid is slightly soluble in ethanol. However, its solubility in ethanol is much lower compared to its solubility in water.
Salicylic acid does not dissolves very easily in hot and cold water. This acid is widely used in acne medicine. It is derived from the bark of the willow tree.
Salicylic acid is a benzene ring with two neighboring functional groups. One is a carboxylic acid (COOH) the other is a hydroxl (OH) When Bicarbonate(HCO3) is added to water with salicylic acid, the -HCO3 pulls the proton off of the hydroxyl making it a salicylate ion. Salicylate ion has a greater solubility than salicylic acid. I think. That's what 1 semester of Ochem will do for you.
I assume you mean in water. Salicylate is a salt of salicylic acid. An organic salt is (pretty much) always more soluble in water than its non-salt counterpart. Water is polar, like dissolves like, etc.
Salicylic acid is soluble in NaOH and insoluble in NaHCO3 and HCl. In NaOH, salicylic acid can form a salt through neutralization. In NaHCO3 and HCl, salicylic acid remains as a solid due to its low solubility in these solutions.
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.
The precipitate of salicylic acid dissolves in excess sulphuric acid due to the formation of a complex between salicylic acid and sulphuric acid, which increases the solubility of the precipitate. This reaction results in the formation of a colorless solution, as the salicylic acid is converted into its conjugate base form.
Salicylic acid, like any other acid, would be dissolved in water.
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.
Sodium hydroxide in a pure form is a solid, so you cannot dissolve anything in it. Normally, NaOH is used as an aqueous solution. But salicylic acid dissolves in water, so the presence of NaOH in the water is irrelevant to the solubility of salicylic acid. It is the water, not the NaOH, that dissolves the salicylic acid.
2,4,6-tribromophenol is formed by the loss of CO2 (decarbonylation).