Chemistry - Carbonyl compounds Question with Solution | TestHub

ChemistryCarbonyl compoundsOxidation of Aldhyde (Tollens, Fehling solution, Baeyer villiger etc. Test)Medium2 minQB
ChemistryMediumsingle choice

Compound 'A' (molecular formula C₃H₈O) is treated with acidified potassium dichromate to form a product 'B' (molecular formula C₃H₆O).

'B' forms a shining silver mirror on warming with ammoniacal silver nitrate.

'B' when treated with an aqueous solution of H₂NCONHNH₂·HCl and sodium acetate gives a product 'C'. Identify the structure of 'C'.

Options:

Answer:
A
Solution:

Solution:

Compound 'A' (C₃H₈O) is a primary alcohol, propan-1-ol. Oxidation with acidified potassium dichromate yields 'B' (C₃H₆O), which is propanal. Propanal gives a silver mirror with Tollens' reagent, confirming it's an aldehyde. Treating propanal with semicarbazide hydrochloride and sodium acetate forms 'C', propanal semicarbazone.

 

The structure of 'C' is:

 

 

Stream:JEESubject:ChemistryTopic:Carbonyl compoundsSubtopic:Oxidation of Aldhyde (Tollens, Fehling solution, Baeyer villiger etc. Test)
2mℹ️ Source: QB

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