An aromatic organic compound 'A' with formula `C_8H_8O` gives positive DNP and iodofrom tests. It neither reduces Tollens' reagent nor does it decolourise bromine water. Write the structure of 'A'. 1

An organic compound A with molecular formula C_8H_8O gives positive DNP and iodoform tests. It does not reduce Tollen’s or Fehling’s reagent and does not decolourise bromine water also. On oxidation with chromic acid (H_2CrO_4) , it gives a carboxy acid (B) with molecular formula C_7H_6O_2 . Deduce the structure of A and B.

An organic compound A with molecular formula C_(9)H_(10)O gives positive DNP and iodoform tests. It does not reduce. Tollen's reagent or Fehling reagent and does not decolourless bromine water or Bayer's reagent. On drastic oxidation with chronic acid, compound A gives a carboxylic acid having molecular formula C_(7)H_(6)O_(2) . Deduce the structur eof organic compound A and write all the chemical reactions involved.

An organic compound (X) with molecular formula C_8H_8O forms an orange red precipitate with 2, 4 - DNP regent and resonds iodoform test. It neither decolourises Baeyer's reagent or bromine water and also it neither reduces Tollen's reagent or Fehling's reagent. Compound (X) gives a carboxylic acid (Y) with molecular formula C_7H_6O_2 on drastic oxidation with chromic acid . Give the equations.

An organic compound containing (x) with molecular formula C_(8)H_(8)O forms an oragne-red precipitate with 2,- -DNP reagent and gives yellow precipitate on heating with ioxdine in the presence of sodium hydroxide. It neither reduces Tollen's Fehlling's reagent, nor does it decolouries bromine water or Baeyer's reagent. On drastic oxidation with chromic acid, it gives a carboxylic acid (Y) having molcular formula C_(7)H_(6)O_(2) . Identify the compounds X and Y.

An organic compound (A) with molecular formula C_(8)H_(8)O forms an orange-red precipitate with 2,4-DNP reagent and gives yellow precipitate on heating with iodine in the presence of sodium hydroxide. It neither reduces Tollens’ or Fehlings’ reagent, nor does it decolourise bromine water or Baeyer’s reagent. On drastic oxidation with chromic acid, it gives a carboxylic acid (B) having molecular formula C_(7)H_(6)O_(2) . Identify the compounds (A) and (B) and explain the reactions involved.

An organic compound (A) with molecular formula C_(8)H_(8)O forms an orange-red precipitate with 2,4-DNP reagent and gives yellow precipitate on heating with iodine in the presence of sodium hydroxide. It neither reduces Tollens or Fehlings reagent, nor does it decolourise bromine water or Baeyerâs reagent. On drastic oxidation with chromic acid, it gives a carboxylic acid (B) having molecular formula C_(7)H_(6)O_(2) . Identify the compounds (A) and (B) and explain the reactions involved.

An organic compound 'X' C_(8)H_(8)O forms an orange-red precipitate of 2, 4-DNP and gives yellow precipitate with iodine and aqueous sodium carbonate on heating. It neither reduces Tollens or Fehlings reagent, nor does it decolourise bromine water or Baeyers reagent. On drastic oxidation wtih chromic acid, it gives a carboxylic acid 'Y' (C_(7)H_(6)O_(2)) . Compounds X and Y are