An alcohol A (C4H10O) on oxidation with acidified potassium dichromate gives carboxylic acid B (C4H8O2). Compound A when dehydrated with conc.H2SO4 at 443K gives compound C. Treatment of C with aqueous H2SO4 gives compound D (C4H10O) which is an isomer of A. Compound D is resistant to oxidation but compound A can be easily oxidized. Identify the compounds and write their structures.
Please write the reactions urself. I m just identifying A, B, C and D. So, A is 2-methyl propan-1-ol. B is 2-methyl propanoic acid. C is 2-methyl prop-1-ene. D is 2-methyl propan-2-ol which is resistant to oxidation.
