An organic compound A `(C_3H_6O)` is resistant to oxidation but forms compound B `(C_3H_8O)` on reduction. 'B' reacts with HBr to form the compound 'C'. C with Mg forms Grignard reagent 'D' which reacts with 'A' to forms a product which on hydrolysis gives. E. Identify A to E

A compound X(C_2H_4O) on oxidation gives Y(C_2H_4O_2) . 'X' undergoes haloform reaction. On treatment with HCN, 'X' forms a product 'Z' which on hydrolysis given 2-Hydroxypropanoic acid.

An aromatic compound (A) on treatment wth aqueous ammonia and heating forms a compound (B) which on heating with Br_2 and KOH froms a compound (c) of molecular formula C_6H_7N . Write the structures and IUPAC names of compounds.

Which of the transition metal forms green compound in its +3 oxidation state and yellow to orange compound in +6 oxidation state?

An organic compound X(C_2H_4O) , on oxi-dation, gives Y(C_2H_4O_2) . Compound (X) undergoes haloform reaction. On treatment with HCN, compound (X) produces Z which on hydrolysis, gives 2-Hydroxypropanoic acid. Write the equation for the reactions involved. What happens when X is treated with dilute NaOH?

An organic compound A on treatment with ethanol yields a carboxylic acid B and a neutral compound C.On hydrolysis, C produces B and another compound D. D on oxidation produces B, which on heating with Ca (OH)_2 gives E (C_3H_6O) E form 2,4 Dinitrophenyl hydrazone derivatives but does not show Fehling test.

A Ketone 'A' Which undergoes haloform reac-tion gives compound B on reduction. B oheatign with H_2SO_4 gives compound C, which forms mono-ozonide D. D on hydroly-sis in presence of Zn dust gives only acetaldehyde. Identify A, B and C. Write down the reactions involved.

An organic compound contains A(C_7H_5N) on hydrolysis with strong aqueous acid gives another compound B which is a monobasic aromatic carboxylic acid. The compound B on treatment with ammonia gives a salt which on heating gives C. The compound C undergoes Hofmann's bromamide reaction to yield aniline. Name A, B and C and write the chemical reactions involved.

An organic compound 'A' having molecular formula C_6H_6O gives a characteristic colour with aqeuous FeCI_3 solution. When 'A' is treated with CO_2 and NaOH at 400K under pressure 'B' is obtained. The compound B on acidification gives compound C which react with acetyl chloride to form D which is a popular pain killer. Deduce the structure of A, B, C and D.

A sweet smelling organic compound 'A' is slowly oxidised by air in presence of light to a higly posionous gas. On warming compound A with silver powder, it forms a gaseous substance 'B' which is also produced by the action of calcium carbide on water. identify 'A' and 'B' and write the chemical reactions involved.

An organic compound has the molecular formula C_5H_(10)O . The compound does not reduce Tollen's reagent but reacts with Brady's re-agent to give orange precipitate. On vigorous Oxidation, the molecule produces ethanoic acid and propanoic acid. The com-pound also gives iodoform test. Identify the compound and write equations for chemical reactions involved.