Benzaldehyde is the simplest aromatic aldehyde. The oxidizing agent used in Fehling's solution is not strong enough to oxidize the aromatic ring. Therefore Benzaldehyde doesn't show Fehling's test. I hope it helped :)
Fehling test is only suitable for reducing sugars, that means, monosaccharides in its open form with an aldehyd available. Polysacchardes have the aldehydes in a acetal form and they can not react
Fehling's test is used to differentiate between aldehyde and ketones group. An aldehyde group will react with Fehling's reagent to give cuprous oxide resulting in a red precipitate. A Ketone group will not react with Fehling's reagent.
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.
Cu2O gives red ppt when heated with fehlings soln
Benzaldehyde has a benzene ring where formaldehyde has a hydrogen atom. (C6H5CHO as opposed to HCHO). Formaldehyde is used as a biocide and a disinfectant. It is a nasty substance and may be a carcinogen. Benzaldehyde on the other hand is used as a food additive to give an almond flavour.
Formalin gives a positive Fehling's solution test.
Aromatic aldehydes, such as benzaldehyde, typically do not give a positive Fehling's test due to the lack of alpha-hydrogens required for oxidation. Aromatic aldehydes are not easily oxidized in the Fehling's test compared to aliphatic aldehydes.
Fehling test is only suitable for reducing sugars, that means, monosaccharides in its open form with an aldehyd available. Polysacchardes have the aldehydes in a acetal form and they can not react
Fehling's test is used to differentiate between aldehyde and ketones group. An aldehyde group will react with Fehling's reagent to give cuprous oxide resulting in a red precipitate. A Ketone group will not react with Fehling's reagent.
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.
Cu2O gives red ppt when heated with fehlings soln
The reduction of D-glucose with Fehling's solution involves two separate reactions. Firstly, glucose is oxidized by Cu²⁺ ions in Fehling's A solution to form a carboxylic acid and Cu₂O. This reaction can be represented by: C₆H₁₂O₆ + 2Cu²⁺ → 2Cu₂O + 2H⁺ + 2CH₂O₂. The Cu₂O formed then reacts with the hydroxide ions in Fehling's B solution to give a red precipitate of copper(I) oxide, Cu₂O, in the final equation: Cu₂O + 2OH⁻ → 2Cu₂O + H₂O.
Starch does not give a positive result in the Fehling test because starch is a polysaccharide made up of glucose units linked together in a way that does not allow the formation of free aldehyde or ketone groups required for the Fehling test to detect reducing sugars. Since starch is a larger molecule, it does not react with the Fehling reagent designed to detect the presence of smaller reducing sugars like glucose and fructose.
Aldehydes give a positive result in Fehling's test because they can be oxidized to carboxylic acids, reducing the Cu^2+ ions in the Fehling's solution to insoluble Cu2O, which forms a brick-red precipitate. In contrast, ketones are generally resistant to oxidation under the mild conditions of the test and do not undergo a similar reduction, leading to a negative result. This difference in reactivity is primarily due to the structure of aldehydes, which have a hydrogen atom attached to the carbonyl carbon, making them more susceptible to oxidation.
Due to absence of free hemiacetal group
Benzaldehyde has a benzene ring where formaldehyde has a hydrogen atom. (C6H5CHO as opposed to HCHO). Formaldehyde is used as a biocide and a disinfectant. It is a nasty substance and may be a carcinogen. Benzaldehyde on the other hand is used as a food additive to give an almond flavour.
Because it is a polymer of formaldehyde with no free aldehydic group.