Testing for Carbonyl Compounds (OCR A Level Chemistry A): Revision Note

Exam code: H432

Stewart Hird

Written by: Stewart Hird

Reviewed by: Caroline Carroll

Updated on

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

    Carbonyl Compounds 2,4-DNPH, downloadable AS & A Level Chemistry revision notes

Ketones and aldehydes react with 2,4-DNPH in a condensation reaction

Carbonyl Compounds Positive-Negative Test, downloadable AS & A Level Chemistry revision notes

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

The Agions 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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Stewart Hird

Author: Stewart Hird

Expertise: Chemistry Content Creator

Stewart has been an enthusiastic GCSE, IGCSE, A Level and IB teacher for more than 30 years in the UK as well as overseas, and has also been an examiner for IB and A Level. As a long-standing Head of Science, Stewart brings a wealth of experience to creating Topic Questions and revision materials for Save My Exams. Stewart specialises in Chemistry, but has also taught Physics and Environmental Systems and Societies.

Caroline Carroll

Reviewer: Caroline Carroll

Expertise: Head of Content Delivery

Caroline graduated from the University of Nottingham with a degree in Chemistry and Molecular Physics. She spent several years working as an Industrial Chemist in the automotive industry before retraining to teach. Caroline has over 12 years of experience teaching GCSE and A-level chemistry and physics. She is passionate about delivering high-quality resources to help students achieve their full potential.