[" An aromatic organic compound 'A' with molecular formula "C_(8)H_(8)O" gives positive DNP and iodoform "],[" tests.It neither reduces Tollens' reagent nor does it decolourise bromine water.Write the structure "],[" of "A" ."]

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_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.

A organic compound with the molecular formula C_(3)H_(6)O does not respond positively to the silver mirror test with Tollens reagent but produces on oxmime. The compound is

A compound (A) with molecular formula C_4H_8O shows bromine water test. Compound (A) is :

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.