Testing for Carbonyl Compounds (OCR A Level Chemistry A): Revision Note
Using 2,4-Dinitrophenylhydrazine
2,4-dinitrophenylhydrazine (also known as 2,4-DNPH) is a reagent which detects the presence of carbonyl compounds (compounds with -C=O group)
The carbonyl group of aldehydes and ketones undergoes a condensation reaction with 2,4-dinitrophenylhydrazine
A condensation reaction is a reaction in which two molecules join together and a small molecule (such as H2O or HCl) is eliminated
The product formed when 2,4-DNPH is added to a solution that contains an aldehyde or ketone is a deep-orange precipitate which can be purified by recrystallisation
The melting point of the formed precipitate can then be measured and compared to literature values to find out which specific aldehyde or ketone had reacted with 2,4-DNPH
Ketones and aldehydes react with 2,4-DNPH in a condensation reaction
![Carbonyl Compounds Positive-Negative Test, downloadable AS & A Level Chemistry revision notes](https://cdn.savemyexams.com/cdn-cgi/image/f=auto,width=3840/https://cdn.savemyexams.com/uploads/2020/12/3.5-Carbonyl-Compounds-Positive-Negative-Test.png)
The test tube on the left shows a negative 2,4-DNPH test and the tube on the right shows a positive test
Examiner Tips and Tricks
The 2,4-DNPH test is especially useful as other carbonyl compounds such as carboxylic acids and esters do not give a positive result
Using Tollens' Reagent
Tollens' reagent contains the silver(I) complex ion [Ag(NH3)2]+
This is formed when aqueous ammonia is added to a solution of silver nitrate
Tollens' reagent is also known as ammoniacal silver nitrate
If gently warmed with Tollens' reagent, an aldehyde will become oxidised
The silver(I) complex ion solution, [Ag(NH3)2]+, is colourless
As the aldehyde is oxidised, it causes the [Ag(NH3)2]+ ions to become reduced to solid metallic silver, Ag
This is why a positive test result is called a "silver mirror"
Positive Test Result:
When Tollens' reagent is gently warmed with an aldehyde, the silver mirror is formed
This is the positive test result
When Tollens' reagent is gently warmed with a ketone, no silver mirror will be seen, as the ketone cannot be oxidised by Tollens' reagent, so no reaction takes place
This is a negative test result
![3-5-4-tollens-reagent-new](https://cdn.savemyexams.com/cdn-cgi/image/f=auto,width=3840/https://cdn.savemyexams.com/uploads/2023/04/3-5-4-tollens-reagent-new.png)
The Ag+ ions in Tollens’ reagent are oxidising agents, oxidising the aldehyde to a carboxylic acid and getting reduced themselves to silver atoms
Examiner Tips and Tricks
Use 2,4-DNP to identify if the compound is a carbonyl
Then to differentiate an aldehyde from a ketone use Tollens' reagent.
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