Benzoic acid is a carboxylic acid that is typically solid at room temperature and has a characteristic acidic smell. Methyl benzoate is an ester that is usually a liquid at room temperature and has a sweet, fruity odor. A chemical test like adding a base to benzoic acid to form a salt or reacting methyl benzoate with an alcohol to get back the carboxylic acid can help distinguish between the two.
One way to distinguish between benzoic acid and phenyl is by performing a sodium bicarbonate test. When sodium bicarbonate is added to benzoic acid, it will effervesce and produce bubbles due to the release of carbon dioxide gas. However, no such effervescence occurs when sodium bicarbonate is added to phenyl. This difference in bubbling can be observed as an obvious physical change to distinguish between the two compounds.
One way to distinguish between benzaldehyde and benzoic acid is by performing a solubility test. Benzaldehyde is soluble in organic solvents, while benzoic acid is soluble in water. Another test is to add aqueous sodium bicarbonate: benzoic acid will effervesce as carbon dioxide gas is produced, whereas benzaldehyde will not show any reaction. Additionally, benzoic acid will give a characteristic white precipitate when treated with acidified potassium permanganate solution, while benzaldehyde will not react with this reagent.
Solubility of benzoic acid in acetone is 1.350 M
To extract benzoic acid from chloroform, first dissolve the benzoic acid in water. Then, add chloroform to the mixture and shake well to allow for the benzoic acid to transfer to the chloroform phase. Finally, separate the two phases and evaporate the chloroform to obtain the benzoic acid.
The trade name for benzoic acid is E210.
Benzoic acid will give brisk effervescence on reacting with sodium bicarbonate.
One way to distinguish between benzoic acid and phenyl is by performing a sodium bicarbonate test. When sodium bicarbonate is added to benzoic acid, it will effervesce and produce bubbles due to the release of carbon dioxide gas. However, no such effervescence occurs when sodium bicarbonate is added to phenyl. This difference in bubbling can be observed as an obvious physical change to distinguish between the two compounds.
One way to distinguish between benzaldehyde and benzoic acid is by performing a solubility test. Benzaldehyde is soluble in organic solvents, while benzoic acid is soluble in water. Another test is to add aqueous sodium bicarbonate: benzoic acid will effervesce as carbon dioxide gas is produced, whereas benzaldehyde will not show any reaction. Additionally, benzoic acid will give a characteristic white precipitate when treated with acidified potassium permanganate solution, while benzaldehyde will not react with this reagent.
the chemical structure of the two are analogous
Benzoic acid is soluble in kerosene.
Solubility of benzoic acid in acetone is 1.350 M
To extract benzoic acid from chloroform, first dissolve the benzoic acid in water. Then, add chloroform to the mixture and shake well to allow for the benzoic acid to transfer to the chloroform phase. Finally, separate the two phases and evaporate the chloroform to obtain the benzoic acid.
Neither. Benzoic acid is... benzoic acid. Intensive and extensive are properties are characteristics of elements and compounds such as color, density, odor, conductivity, etc. To say benzoic acid is extensive or benzoic acid is intensive doesn't make sense.
O-hydroxy benzoic acid or 2-hydroxy benzoic acid.
The trade name for benzoic acid is E210.
Benzoic acid
depends on how much benzoic acid you use. if you have 0.5g of benzoic acid , you need 30ml of water as a solvent.