An Organic Compound (A) Having Molecular Formula C9H10O Forms ...

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SolveGuidesJoin / LoginUse appLogin0You visited us 0 times! Enjoying our articles? Unlock Full Access!Standard XIIChemistryChemical Reactions of Aldehydes and KetonesQuestionAn organic compound $$(A)$$ having molecular formula $$C_{9}H_{10}O$$ forms an orange reed precipitate $$(B)$$ with $$2, 4-DNP$$ reagent. Compound $$(A)$$ gives a yellow precipitate $$(C)$$ when heated in the presence of iodine and $$NaOH$$ along with a colourless compound $$(D)$$. $$(A)$$ does not reduce Tollens reagent of Fehling's solution nor does it decolourise bromine water. On drastic oxidation of $$(A)$$ with chromic acid, a carboxylic acid $$(E)$$ of molecular formula $$C_{7}H_{6}O_{2}$$ is formed.Deduce the structures of the organic compounds $$(A)$$ to $$(E)$$.Open in AppSolutionVerified by TopprWas this answer helpful?16Similar QuestionsQ1An organic compound $$(A)$$ having molecular formula $$C_{9}H_{10}O$$ forms an orange reed precipitate $$(B)$$ with $$2, 4-DNP$$ reagent. Compound $$(A)$$ gives a yellow precipitate $$(C)$$ when heated in the presence of iodine and $$NaOH$$ along with a colourless compound $$(D)$$. $$(A)$$ does not reduce Tollens reagent of Fehling's solution nor does it decolourise bromine water. On drastic oxidation of $$(A)$$ with chromic acid, a carboxylic acid $$(E)$$ of molecular formula $$C_{7}H_{6}O_{2}$$ is formed.Deduce the structures of the organic compounds $$(A)$$ to $$(E)$$.View SolutionQ24.An organic compound( A )having molecular formula C9H10O forms an organic red precipitate (B) with 2;4 DNP reagent . compound( A )gives yellow precipitate (C) when heated in the presence of iodine and NaOH along With colourless compound (D) .A does not reduce tollen's reagent or Fehling 's solution nor does it decolorizes bromine water . On drastic oxidation of (A )with chromic acid ,a carboxylic acid (E)of molecular Formula C7H6O2 is formed Deduce the structure of the organic compounds (A) to( E )View SolutionQ3An organic compound (A) with molecular formula C8H8O 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 Fehling's 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 C7H6O2. Identify the compounds (A) and (B) and explain the reactions involved. View SolutionQ4An organic compound (A) having molecular formula C9H10O forms orange-red ppt (B) with the 2,4-DNP reagent. Compound (A) gives yellow ppt (C) when heated in the presence of iodine and NaOH along with a colorless compound (D). (A) does not reduce Tollen's reagent or Fehling's solution nor does it decolorize the Br2 water. On drastic oxidation of (A) with chromic acid, carboxylic acid (E) of molecular formula C7H6O2 is formed. Identify A to EView SolutionQ5an organic compound (a) with molecular formula C8H80 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 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 C7H6O2. identify the compounds (a) and (b) and explain the reactions involved.View Solution

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