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Testing for Carbonyl Compounds (CIE AS Chemistry)

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Philippa

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Testing for Carbonyls: 2,4-DNPH

  • 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

Example reaction of a ketone 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

 

Results of chemical tests using 2,4-DNPH

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

Exam Tip

The 2,4-DNPH is especially useful as other carbonyl compounds such as carboxylic acids and esters do not give a positive test

Identifying Carbonyls: Fehling's Solution & Tollens' Reagent

  • The presence of an aldehyde group (-CHO) in an unknown compound can be determined by the oxidising agents Fehling’s and Tollens’ reagents

Fehling’s solution

  • Fehling’s solution is an alkaline solution containing copper(II) ions which act as the oxidising agent
  • When warmed with an aldehyde, the aldehyde is oxidised to a carboxylic acid and the Cu2+ ions are reduced to Cu+ ions 
    • In the alkaline conditions, the carboxylic acid formed will be neutralised to a carboxylate ion (the -COOH will lose a proton to become -COO- )
    • The carboxylate ion (-COO-) will form a salt with a positively charged metal ion such as sodium (-COO-Na+)

  • The clear blue solution turns opaque due to the formation of a red precipitate, copper(I) oxide
  • Ketones cannot be oxidised and therefore give a negative test when warmed with Fehling’s solution

Colour change using Fehling's solution

Carbonyl Compounds Fehlings Solution, downloadable AS & A Level Chemistry revision notes

The copper(II) ions in Fehling’s solution are oxidising agents. They can oxidise an aldehyde to a carboxylic acid and are themselves reduced to copper(I) ions in the Cu2O precipitate

Tollens’ reagent

  • Tollens' reagent is an aqueous alkaline solution of silver nitrate in excess ammonia solution
    • Tollens' reagent is also called ammoniacal silver nitrate solution

  • When warmed with an aldehyde, the aldehyde is oxidised to a carboxylic acid and the Ag+ ions are reduced to Ag atoms
    • In the alkaline conditions, the carboxylic acid will become a carboxylate ion and form a salt

  • The Ag atoms form a silver ‘mirror’ on the inside of the tube
  • Ketones cannot be oxidised and therefore give a negative test when warmed with Tollens’ reagent

Colour change using Tollens' reagent

3-5-4-tollens-reagent-new

The Ag+ ions in Tollens’ reagent are oxidising agents. They can oxidise an aldehyde to a carboxylic acid and are themselves reduced to silver atoms

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Philippa

Author: Philippa

Philippa has worked as a GCSE and A level chemistry teacher and tutor for over thirteen years. She studied chemistry and sport science at Loughborough University graduating in 2007 having also completed her PGCE in science. Throughout her time as a teacher she was incharge of a boarding house for five years and coached many teams in a variety of sports. When not producing resources with the chemistry team, Philippa enjoys being active outside with her young family and is a very keen gardener.