Saponification is a term used where soaps are formed as from fats and oils (triglycerides), methyl benzoate is a simple ester so here we may use the term hydrolysis, the reaction is performed in presence of NaOH so initial products are in ionic or salt form, sodium benzoate and sodium methoxide so are soluble in water.
Saponification is performed with NaOH so products are Methanol and Sodium benzoate both of these are soluble in water.
Methyl benzoate, an organic compound, is an ester. It is a colorless liquid that is not soluble in water and has a fruity smells. Some uses for methyl benzoate are as a solvent and a pesticide.
Soaps make soluble in water fats an oils, forming specific micelles.
All , Because the reaction between oil and alkali takes place only at interface and thus rate of the reaction is very slow . But when oil is dissolved in ethanol the saponification progresses well.
Yes,it can
There is no such thing as carbon trioxide. There is the carbonate ion (CO32-). Most carbonates are insoluble in water. There is also carbon dioxide (CO2) which is somewhat soluble in water.
Methyl benzoate, an organic compound, is an ester. It is a colorless liquid that is not soluble in water and has a fruity smells. Some uses for methyl benzoate are as a solvent and a pesticide.
The solubility of sodium benzoate in water is 62.69 grams per 100 mL. Generally acids are not very soluble in water.
Yes, Benzoic acid is a weak acid (pKa ~ 4.2) that will dissolve in weak base such as sodium bicarbonate (pKa ~ 6.4)
sodium bicarbonate, citric acid,sodium benzoate and water soluble flavour
Soaps make soluble in water fats an oils, forming specific micelles.
Because sodium benzoate is a salt and is soluble in water while benzoic acid is insoluble.
All the products which dissolve in water completely are soluble products like sugar, salt etc while the products which didn't dissolve in water completely are non soluble products like sand, chalk dust etc.
You're starting with something like sodium benzoate (depends on what base you used for the extraction step), which contains sodium ions (Na+) and benzoate ions (C6H5COO-). Ionic compounds like that tend to be soluble in water. When you add H+, you protonate the benzoate ion to make benzoic acid (C6H5COOH), which is a neutral molecule, and hardly soluble in water at all... so it precipitates.
HCl(aq) + C6H5COONa(aq) --> C6H5COOH(s) + NaCl(aq)
One gram of the salt is soluble in 2 ml of water, in 75 ml of ethyl alcohol, and in 50 ml of 90 % ethyl alcohol. The salt is insoluble in ethyl ether. Source is is a pdf from http://www.emeraldmaterials.com The complete link to the pdf file is found to the left of this answer under Web Links. It also includes the solubility in water a variety of temperatures.
Soluble or not soluble, salts are the products of reactions between acids and bases.
Steroids and fat-soluble vitamins are classified as derived lipid since they can be inactivated by saponification reaction, the structure therefore is not ester type but it is an alcohol type.