Aldehydes and ketones have a similar structure. Both possess a carbonyl group, which is a carbon double bonded to an oxygen. An aldehyde has at least one hydrogen connected to the carbonyl carbon. The second group is either a hydrogen or a carbon-based group. In contrast, a ketone has two carbon-based groups connected to the carbonyl carbon. Certain reactions undergone by aldehydes and ketones can be used to distinguish them or identify their functional groups based on visible differences in the reaction's outcome.
One such reaction is the DNPH test, which is used to determine whether an aldehyde or ketone is aromatic. In this reaction, 2,4-dinitrophenylhydrazine, or DNPH, attacks the carbonyl of an aldehyde or ketone in an aqueous acidic solution. This condensation reaction produces a hydrazone, which precipitates from the aqueous solution.
When a non-aromatic ketone or aldehyde reacts with DNPH, the precipitate is yellow. However, aromatic ketones and aldehydes give a red-orange precipitate. DNPH can also be used to distinguish alcohols and esters from aldehydes and ketones since DNPH does not react with alcohols or esters. We call this lack of reaction a negative result.
Another useful reaction is used as the iodoform test for methyl ketones, which are ketones that have at least one methyl as a functional group. When a methyl ketone is mixed with iodine under aqueous alkaline conditions, iodine replaces each methyl hydrogen, making an excellent leaving group. Substitution, followed by proton transfer, converts the leaving group into iodoform, which precipitates from the solution as a pale yellow solid.
This reaction also works for acetaldehyde, which is an aldehyde with methyl as its R group. The reaction relies on the unique reactivity of the hydrogens in an alpha-methyl group, so mixing any other ketone or aldehyde with iodine will not make solid yellow iodoform.
Finally, we can distinguish between ketones and aldehydes using the Tollens test. Diamminesilver(1+), or Tollens' reagent, oxidizes aldehydes to carboxylic acids. Tollens' reagent is reduced to elemental silver in the process, which either coats the inner wall of the test tube or forms a black precipitate. Most ketones, however, are not oxidized by Tollens' reagent, so no solid silver will form.
In this lab, you will identify several unknown aldehydes and ketones by performing the DNPH test, the Tollens test, and the iodoform test.
At the end of this lab, students should know...
A ketone is a carbonyl with two alkyl (or aryl) groups attached. An aldehyde has the same structure as a ketone, except one of the side groups is a hydrogen.
Since the carbonyl carbon is an electrophile, the typical reaction undergone by an aldehyde or ketone is a nucleophilic addition.
The DNPH test is used to indicate the presence of an aldehyde or ketone. Additionally, the DNPH test can distinguish aldehydes and ketones from alcohols or esters, as the latter compounds will not react with DNPH.
Under basic conditions, a methyl ketone reacts with excess halogen. The three methyl hydrogens are substituted by the halogen, which then leave the molecule and form a precipitate. The test gives a negative result for any other ketone or aldehyde, as it requires three hydrogens in the neighboring carbon to proceed.
The Tollens’ test distinguishes between aldehydes and ketones. Tollens’ reagent oxidizes an aldehyde to a carboxylic acid. The silver ion in the Tollens’ reagent is then reduced to solid silver, which coats the walls of the test tube. Ketones do not react with Tollens’ reagent.
Source: Lara Al Hariri at the University of Massachusetts Amherst, MA, USA
Here, we show the laboratory preparation for 10 students working in pairs, with some excess. Please adjust quantities as needed.
| 1Lab stand |
| 1Small 3-prong clamp |
| 1Hotplate |
| 1Vacuum line |
| 1Test tube rack |
| 1Test tube tongs |
| 1600-mL beaker |
| 4250-mL beakers |
| 1150-mL beaker |
| 550-mL beakers |
| 310-mL graduated cylinders |
| 55-mL graduated cylinders |
| 1250-mL filter flask |
| 1Büchner funnel |
| 1Filter adapter |
| 4Small watch glasses |
| 1Glass stirring rod |
| 1Thermometer with beaker clip |
| 3Pipette bulbs |
| 1Package of pH paper |
| 1Roll of lab tape and marking pen |
| 1250-mL bottle of DI water |
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