Chemistry - Carbonyl compounds Question with Solution | TestHub
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'.
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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: