Match each chemical reaction or test involving carbonyl compounds in Column A with its corresponding characteristic visual outcome in Column B.
- Warming ethanal with Fehling's solutionFormation of a brick-red precipitate
- Warming propanone with Tollen's reagentNo visible reaction occurs
- Warming propanal with acidified potassium tetraoxomanganate(VII) solutionDecolorization of the purple solution
- Warming propanone with iodine in sodium hydroxide solutionFormation of a pale yellow precipitate
Answer
Warming ethanal with Fehling's solution yields a brick-red precipitate; warming propanone with Tollen's reagent yields no visible reaction; warming propanal with acidified causes decolorization of the purple solution; and warming propanone with iodine in sodium hydroxide solution produces a pale yellow precipitate.
Alkanals (ethanal and propanal) are reducing agents due to the carbonyl hydrogen atom; thus, ethanal reduces Fehling's solution to a brick-red copper(I) oxide precipitate, and propanal reduces purple acidified to a colorless solution. Alkanones (propanone) lack this hydrogen atom, so propanone shows no reaction with Tollen's reagent. However, because propanone has a group, it responds to the triiodomethane test by forming a pale yellow precipitate.
Step-by-Step Solution
Key Concept
Distinction tests and oxidation properties of alkanals and alkanones
Estimated Time:1m 0s