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 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.
Benzoic acid is more soluble than camphor in ethanol. The solution can be filtrated.
Soluble in acetone, dimethyl formamide, DMSO, dichloromethane, 100% ethanol or methanol; sparingly soluble in water.
yes it will because carbon tetracholride has more dence than sulfuric acid
It depends upon solvent with respect to water, alkenes are not soluble. Carboxylic Acid are soluble but they become less soluble as the chain length increases due to the longer non-polar hydrocarbon chain which can't form hydrogen bonds with water.
salicylic acid (an acid) is more polar than methyl salicylate (an ester)
Salicylic acid, like any other acid, would be dissolved 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 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.
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.
Salicylic acid has a hydroxyl group (-OH) attached to the benzene ring, while benzoic acid has a carboxylic acid group (-COOH) attached to the benzene ring. This difference results in salicylic acid being a phenol derivative and having different chemical properties compared to benzoic acid.
Aspirin is considered more effective than salicylic acid because it is a modified form of salicylic acid that is easier for the body to absorb and has fewer side effects. This modification allows aspirin to be more targeted in its pain-relieving and anti-inflammatory effects, making it a preferred medication for many conditions.
To prepare a 2 molar salicylic acid solution, you would need to dissolve 17.5 grams of salicylic acid in enough water to make 1 liter of solution. First, measure out the salicylic acid using a balance, then add it to a beaker or flask with some water and stir until dissolved. Finally, add more water to bring the volume up to 1 liter, and mix well to ensure uniform concentration.
Using a Vernier Conductivity Probe the Salcylic Acid dissolved in water gave a value of 1172 microS/cm (this value may change depending on the concentration of Salicylic Acid in the solution). The conductance of distilled water is 6 microS/cm. So it does increase the conductance but not as much as ionic substances such as table salt which would give 3760 microS/cm.
,,,plants have small amount of salicylic acid,,,but the willow tree have more salicylic to be used in making an aspirin,,,researchers said that willow tree is the only tree having more salicylic acid
In salicylic acid the hydrogen atom in OH group have a tendency to form hydrogen bonding with oxygen atom in the COO - group thus leaving the H+ ion freely available. In case of ortho methoxy benzoic acid, the possibility of hydrogen bonding is avoided by the presence of strong -CH3 group. Hence salicylic acid is stronger than ortho methoxy benzoic acid.
Yes, ethanoic acid (acetic acid) is more soluble in water than hexanoic acid. This is because ethanoic acid is a smaller molecule with a polar carbonyl group, allowing it to form hydrogen bonds with water molecules more easily compared to hexanoic acid.