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 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 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 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_(9)H_(10)O forms an arage-red precipitate [B] with 2,4 DNP reagent. Compound [A] gives yellow precipiatate [C] on heating wihth iodine in the presence of soedium hydroxide along with a colourless compound [D]. The compound [A] does not reduce Tollen's reagent or Fehling's solution nor does it decolourise bromine water or Baeyer's reagent. On drastic oxidation with chromic acid, compound [A] gives a crboxylic acid [E] having molecular formula C_(7)H_(6)O_(2) . Deduce the strcutres of the organic compounds [A] to [E].

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 (A) with molecular formula C_8H_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 Tollen's reagent or Fehling's solution , nor does it decolourise bromine water or Baeyer's reagent. On drastic oxidation with chromic acid, it gives a carboxylic acid (B) having molecular formulae C_7H_6O_2 . Identify the compound (A) and (B) and explain the reactions involved .

An organic compound (A) with molecular formula C_8H_8O forms an orange precipitate with 2, 4 dinitrophenyl hydrazine and gives yellow precipitate on heating with iodine in presence of sodium hydroxide. It neither reduces Tollen's reagent nor Fehling solution and it also does not decolourise bromine water or Baeyer's reagent. On drastic oxidation with chromic acid it gives a carboxylic acid (B) having molecular formula C_7H_6O_2 . Identify the compound (A) and (B) and explain in detail the reactions involved