The reaction between acid(benzoic acid) and base(propan-2-ol) gives salt and water. The water being produced means it is a condensation reaction. This reaction is reversible.
Forward reaction= Condensation
Backward reaction= Hydrolysis
Word equation:
Benzoic acid + Propan-2-ol = 1-methylethyl benzoate + water
Chemical Equation:
C6H5COOH + CH3(CHOH)CH3 = C6H5COOCH(CH3)2 + H2O
HCl + NaOH = H2O + NaCl Or, water and table salt--which will dissolve in water. Benzoic acid, C6H5COOH, will not be formed; neither of the two starting chemicals contains carbon, and benzoic acid contains a lot of it. - - - - - Benzoic acid and sodium chloride
The derivative of benzoic acid is sodium benzoate, which is often used as a preservative in food and beverages due to its antimicrobial properties. Sodium benzoate is the sodium salt of benzoic acid and is more soluble in water than benzoic acid itself.
In regular Mello Yello there is no benzoic acid. There may be in diet or other variations of the brand. In order to find out how much is in it you will need to contact Coca-Cola. There should be a contact number on the product.
When Benzoic acid is heated beyond its boiling point, it starts precipitating snow like solids.
Ammonium benzoate is an organic salt of benzoic acid. This salt may be formed by reacting benzoic acid with liquid ammonia, C6H5-COOH + NH3 = C6H5-COO-(NH4+) Benzoic acid and benzoates are sometimes used in foods or beverages as preservatives.
The product formed when benzoic acid reacts with ethanol is ethyl benzoate, along with water. This reaction is an esterification process, where the -OH group of the benzoic acid reacts with the -OH group of ethanol to form the ester and water as a byproduct.
When benzoic acid reacts with sodium bicarbonate, it results in the formation of sodium benzoate, carbon dioxide gas, and water. This reaction is an example of an acid-base reaction where the benzoic acid (acid) reacts with sodium bicarbonate (base) to form sodium benzoate (salt) and carbon dioxide gas.
benzoic acid + Sodium Hydroxide ==> water + sodium benzoate
Yes, benzoic acid is soluble in NaOH because when it reacts with NaOH, it forms the water-soluble salt sodium benzoate.
When benzoic acid reacts with neutral ferric chloride, the resulting reaction forms a complex between the ferric chloride and benzoic acid. This complex is a purple-colored compound known as ferric benzoate, signifying the coordination of the iron ion with the carboxylic group of benzoic acid.
C6H5COOH + NaOH + I2 -----------> C6H5COOI + NaI + H2O
When ethanol and benzoic acid combine, the products depend on the reaction conditions. Under acidic conditions, esterification can occur producing ethyl benzoate and water. Under basic conditions, the sodium salt of benzoic acid may form.
Toluene reacts with acidic permanganate on heating and forms the Benzoic acid.
HCl + NaOH = H2O + NaCl Or, water and table salt--which will dissolve in water. Benzoic acid, C6H5COOH, will not be formed; neither of the two starting chemicals contains carbon, and benzoic acid contains a lot of it. - - - - - Benzoic acid and sodium chloride
The product formed would be benzoic acid. Ethyl benzoate reacts with water in the presence of hydrochloric acid and heat to undergo hydrolysis, breaking the ester bond. This results in the formation of benzoic acid and ethanol.
Benzoic acid is soluble in kerosene.
Benzoic acid has a chemical formula of PhCOOH. It does not react with water so much as it dissociates in it, forming a free hydrogen ion. The reaction for the dissociation is PhCOOH(aq) --> PhCOO-(aq) + H+ (aq).