Saponification is the hydrolysis of fat in presence of caustic soda (NaOH), the products are Soap and Glycerin
CH2-CO-R1 CH2-OH R1-COONa
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CH-CO-R2 + 3NaOH --------> CH-OH + R2-COONa
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CH2-CO-R3 CH2-OH R3-COONa
(Fat) (Glycerin) (Soap)
In organic chemistry, NaOH (sodium hydroxide) can undergo key reactions such as nucleophilic substitution, elimination, and saponification. Nucleophilic substitution involves the replacement of a leaving group by the hydroxide ion from NaOH. Elimination reactions involve the removal of a proton and a leaving group to form a double bond. Saponification is a reaction where NaOH reacts with esters to form soap and alcohol.
When an ester is reacted with NaOH, it undergoes hydrolysis to form the corresponding carboxylate salt and alcohol. The reaction is typically called saponification and is often used in the production of soap.
Tripalmitin is a 16 carbon saturated fatty acid. Saponification is a reaction involving a strong base (ex: NaOH) and a fatty acid. The reaction yields a glycerol and 3 fatty acid salts. Therefore the reaction products are: glycerol: CH2(OH)--CH(OH)--CH2(OH) + 3 fatty acid salts: CH3--(CH2)14--COO(-) Na(+) + 3H2O Above is actually a summary of what is in reality a 2-step reaction: the fatty acid reacts with H2O first to yield a glycerol and 3 fatty acids; the fatty acids subsequently reacts with the alkaline (base) (NaOH) to yield 3 fatty acid salts and H2O
Base hydrolysis of an ester is known as saponification, where the ester is hydrolyzed in the presence of a strong base (e.g. NaOH) to form a carboxylate salt and an alcohol. This reaction is commonly used in soap-making processes.
Yes, oleic acid is soluble in dilute NaOH due to the formation of soap through saponification reaction. Oleic acid reacts with NaOH to form the sodium salt of oleic acid, which is a soap that is water-soluble.
what happen when fatti acid react with the NaOH
The initial products of saponification of methyl benzoate are the sodium salt of benzoic acid and methanol. The sodium salt of benzoic acid is soluble in water because it forms ionic bonds with water molecules. Methanol is also soluble in water due to its polar nature, allowing it to hydrogen bond with water molecules.
In organic chemistry, NaOH (sodium hydroxide) can undergo key reactions such as nucleophilic substitution, elimination, and saponification. Nucleophilic substitution involves the replacement of a leaving group by the hydroxide ion from NaOH. Elimination reactions involve the removal of a proton and a leaving group to form a double bond. Saponification is a reaction where NaOH reacts with esters to form soap and alcohol.
When an ester is reacted with NaOH, it undergoes hydrolysis to form the corresponding carboxylate salt and alcohol. The reaction is typically called saponification and is often used in the production of soap.
2
Ethyl Alcohol + Ethanoic Acid
The catalyst needed for saponification is typically an alkali, such as sodium hydroxide (NaOH) or potassium hydroxide (KOH). These alkalis help to hydrolyze ester bonds in fats or oils, leading to the formation of soap.
Tripalmitin is a 16 carbon saturated fatty acid. Saponification is a reaction involving a strong base (ex: NaOH) and a fatty acid. The reaction yields a glycerol and 3 fatty acid salts. Therefore the reaction products are: glycerol: CH2(OH)--CH(OH)--CH2(OH) + 3 fatty acid salts: CH3--(CH2)14--COO(-) Na(+) + 3H2O Above is actually a summary of what is in reality a 2-step reaction: the fatty acid reacts with H2O first to yield a glycerol and 3 fatty acids; the fatty acids subsequently reacts with the alkaline (base) (NaOH) to yield 3 fatty acid salts and H2O
Base hydrolysis of an ester is known as saponification, where the ester is hydrolyzed in the presence of a strong base (e.g. NaOH) to form a carboxylate salt and an alcohol. This reaction is commonly used in soap-making processes.
Yes, oleic acid is soluble in dilute NaOH due to the formation of soap through saponification reaction. Oleic acid reacts with NaOH to form the sodium salt of oleic acid, which is a soap that is water-soluble.
When a fatty acid is reacted with NaOH, a process called saponification occurs. This reaction results in the formation of soap, which is a salt of the fatty acid alongside glycerol. This reaction is commonly used in soap-making processes.
Insoluble soaps are not likely to exist, they won't work when not IN water. For more you can trust on this: his process is called saponification: fat + sodium hydroxide -> Sodium salts of fatty acid (Soap) + glycerol