Home
Class 12
CHEMISTRY
An organic compound (P) having molecular...

An organic compound (P) having molecular formula `C_(9)H_(10)O` form an orange precipitate (Q) with 2,4-DNP reagent. Compound (P) gives a yellow precipitate (R ) when heated in the presence of iodine and NaOH along with a colourless compound (S). (P) neither reduce Tollen's reagent or Fehling's solution nor it decolourises bromine water.
On drastic oxidation of (P) with chromic acid, a carboxylic acid (T) having molecular formula `C_(7)H_(6)O_(2)` is obtained. Deduce the structures of the compounds (P) to (T).

Promotional Banner

Topper's Solved these Questions

  • CARBOXYLIC ACIDS

    ARIHANT PUBLICATION|Exercise CHAPTER PRACTICE (SHORT ANSWER TYPE II QUESTIONS)|6 Videos
  • ARYL DIAZONIUM SALTS

    ARIHANT PUBLICATION|Exercise CHAPTER PRACTICE (LONG ANSWER TYPE QUESTIONS) 7 MARKS |2 Videos
  • CHEMICAL KINETICS

    ARIHANT PUBLICATION|Exercise CHAPTER PRACTICE (Long Answer Type Questions)|8 Videos

Similar Questions

Explore conceptually related problems

The compound having molecular formula C_4H_10O can show:

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

An alcohol having molecular formula, C_(4)H_(9)Br is optically active. What is its structure?