An unknown aldehyde 'A' on reacting with alkali gives a `beta` hydroxy aldehyde, which losses water to form an unsaturated aldehyde, but-2-enal. Another aldehyde 'B' undergoes disproportionation reaction in the presence of conc alkali to form products 'C' and 'D'. 'C' is an aryl alcohol with formula `C_7H_8O`: Identify A and B.

An unknown aldehyde 'A' on reacting with alkali gives a beta hydroxy aldehyde, which losses water to form an unsaturated aldehyde, but-2-enal. Another aldehyde 'B' undergoes disproportionation reaction in the presence of conc alkali to form products 'C' and 'D'. 'C' is an aryl alcohol with formula C_7H_8O : Name the product, when 'B' reacts with zinc amalgam and hydrochloric acid.

An unknown aldehyde 'A' on reacting with alkali gives a beta hydroxy aldehyde, which losses water to form an unsaturated aldehyde, but-2-enal. Another aldehyde 'B' undergoes disproportionation reaction in the presence of conc alkali to form products 'C' and 'D'. 'C' is an aryl alcohol with formula C_7H_8O : Write the sequence of reactions involved

A blackish brown coloured solid 'A' when fused with alkali metal hydroxides in presence of air, produces a dark green coloured compound 'B' which on electrolytic oxidation in alkaline medium gives a dark purple coloured compound 'C' Identify A, B and C and write the reactions involved.

Two moles of organic compound 'A' on teratment with a strong base give two compounds 'B' and 'C'. Compound 'B' on dehydrogenation with Cu gives 'A' while acidification of 'C' yield carboxylic acid 'D' with molecular formula of CH_2O_2 . Identify the compounds A, B, C and D. Write all chemical reactions involved.

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 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.

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.

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.

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