Aldehydes and ketones are two types of organic molecules in the carbonyl group. RCH(=O) is the structure of an aldehyde, whereas R2C(=O) is the structure of a ketone. R can represent any of the following groups: alkyl, alkenyl, alkynyl, or aryl. Many different tests help to distinguish between chemical compounds. Applying the same test to all cases is not a suitable approach. Therefore, it is important to know how to choose the most appropriate test. Only then can the difference between the compounds become clear.
Definition
Aldehydes are compounds with a double bond between carbon and oxygen atoms, represented by the formula (R-(C=O)-H), where ‘R’ represents the alkyl group and ‘H’ represents the hydrogen atom.
Ketones are chemical molecules with the carbonyl group C=0 and alkyl groups on both sides. Because they lack hydrogen atoms, they are less reactive than aldehydes. Their chemical formula is R-(C=0)-R’, where R and R’ are alkyl groups on the left and right sides of the molecule, respectively.
Chemical tests to distinguish between aldehydes and ketones
Tollen’s Test: Compounds with an aldehydic group often pass Tollen’s test (aldehydes, alpha-hydroxy ketones and formic acid- it’s COOH- behaves like an aldehydic group). Although significant progress has been made in understanding single monomer polymerization, studies on copolymerization remain limited. On the other hand, nothing is noticed in the case of ketones
Fehling’s test: Fehling’s test can distinguish between reducing and non-reducing carbohydrates. This test can also distinguish between carbohydrates with the ketone functional group and carbohydrates that are water-soluble. When treated with Fehling’s solution, aliphatic aldehydes generate a reddish-brown precipitate (positive result), whereas aromatic aldehydes and ketones do not
Benedict’s Test: This test is utilized to test the presence of reducing sugars in a substance and simple carbohydrates with a free ketone or aldehyde functional group. Reagent used is a complicated mixture of sodium citrate, sodium carbonate, and copper(II) sulphate pentahydrate. This reagent is also called Benedicts reagent
Potassium Dichromate Oxidation: Acidified potassium dichromate solution oxidises aldehydes, turning the orange solution green. Ketones are observed to have no impact
Propanal And Propanone
Propanal is an aldehyde with three carbons. It is also known as propionaldehyde and its chemical formula is CH3CH2CHO.
Propanone is an organic molecule also known as acetone. Its chemical formula is (CH3)2CO. It is the simplest and tiniest in the ketone family.
Chemical tests to distinguish between propanal and propanone
Tollen’s Test: Propanal is classified as an aldehyde. As a result, Tollen’s reagent is reduced. However, the fact that propanone is a ketone has no bearing on Tollen’s reagent.
CH3CH2CHO + 2[Ag(NH3) 2 ] + + 3OH− → CH3CH2COO − + Ag ⏐↓ +4NH3 + 2H2O
Fehling’s Test:
CH3CH2CHO + 2Cu 2+ + 5OH − → CH3CH2COO − + CH3CH2COO − + Cu2O
Iodoform Test: The iodoform test reacts with aldehydes and ketones that have at least one methyl group attached to the carbonyl carbon atom. Iodoforms are formed when sodium hypoiodite (NaOI) oxidises them. Propanone responds to this test since it is a methyl ketone, but propanal does not.
CH3COCH3 + 3NaOI → CH3COONa + CHI3 + 2NaOH
Benzaldehyde And Acetophenone
The aromatic aldehyde benzaldehyde, with the chemical formula, C6H5CHO, is an aromatic aldehyde. A phenyl group is linked to an aldehyde functional group in this compound.
Acetophenone is an organic molecule with the chemical formula, C8H8O. It is a ketone and it is the simplest among aromatic ketones.
Test To Distinguish Between Benzaldehyde And Acetophenone
Tollen’s Test: Acetophenone is an aromatic ketone molecule, while benzaldehyde is an aromatic aldehyde. Since the aldehyde functional group can produce a precipitate with Tollen’s reagent, it is the easiest approach to distinguish between benzaldehyde and acetophenone. Tollen’s reagent can be reduced by benzaldehyde, resulting in a red-brown Cu2O precipitate, whereas acetophenone does not react with Tollen’s reagent.
Tollen’s test causes aldehydes to react. Because benzaldehyde is an aldehyde, it reduces Tollen’s reagent to produce a red-brown Cu2O precipitate, whereas acetophenone is a ketone and does not.
C6H5CHO + 2[Ag(NH3)2 ] +OH − → C6H5COO NH4 + 2Ag ↓ +3NH3 + H2O
Iodoform Test: As a methyl ketone, acetophenone is oxidised by sodium hypoiodite (NaOI) to produce a yellow precipitate of iodoform. Benzaldehyde, on the other hand, does not respond to this test.
C6H5COCH3 + 3NaOI → C6H5COONa + CHI3 + 2NaOH
Benzaldehyde And Benzophenone
Benzaldehyde is an aromatic aldehyde. Its chemical formula is C6H5CHO. A phenyl group is linked to an aldehyde functional group in this compound. It is also the most basic aromatic aldehyde. It comes in the form of a colourless liquid with an almond-like odour.
Benzophenone is an aromatic ketone. Its chemical formula is C13H10O. It is an aromatic ketone with two benzene rings connected to the carbonyl group’s identical carbon atom. It can be abbreviated as Ph2O, with Ph standing for “phenol” (another name for benzene ring).
Benzaldehyde is an aromatic aldehyde with the formula C6H5CHO, whereas benzophenone is an aromatic ketone with the formula, C13H10O. The main distinction between benzaldehyde and benzophenone is that the former is an aldehyde, while the latter is a ketone. In addition, benzaldehyde has an almond-like odour while benzophenone has a geranium-like odour.
The main distinction between benzaldehyde and benzophenone is that the former is an aldehyde, while the latter is a ketone. However, because it is an aldehyde, benzaldehyde contains one phenyl group linked to the carbonyl group because the other side of the carbonyl carbon possesses a hydrogen atom. To Distinguish Between Benzaldehyde And Benzophenone, one can perform any one of the above tests that differentiate between Aldehyde and Ketones.
Conclusion
Thus, it can be concluded that many tests are used to distinguish between aldehydes and ketones. These include Tollen’s test, Fehling’s test, potassium dichromate oxidation and iodoform test. However, the same tests can yield different results for different compounds. This can be seen while testing Therefore, it is important to know how each compound reacts in different tests. Only then can the differences become clear.
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