Carbonyl CompoundHard
Question
Compound A (molecular formula C2H8O) is treated with acidified potassium dichromate to form a product B (molecular formula C2H6O). B forms a shining silver mirror on warming with an aqueous solution of H2NCONHMH2 and sodium acetate gives a product C. Identify the structure of C.
Options
A.CH3CH2CH = N.NHCOH2
B.
C.
D.CH3CH2CH = N.CONHNH2
Solution
A is p-alcohol because its oxidation gives an aldehyde ′B′. B gives shining mirror with ammonical silver nitrate (Tollen′s reagent)
Thus structure of compound A is CH3Ch2CH2OH(M.F. = C3H8O)
Thus structure of compound A is CH3Ch2CH2OH(M.F. = C3H8O)
Create a free account to view solution
View Solution FreeMore Carbonyl Compound Questions
Of the following, which is the product formed when cyclohexanone undergoes aldol condensation followed by heating ?:-...The best method for the conversion of ethanol to ethanal is-...Structutre of ′A′ would be...Consider the following sequence of reactions.Ketone A BC The ketone (A) is...When propyne reacts with 20% H2SO4 & 1% HgSO4 , we get-...