An organic compound 'X' with the molecular formula C₅H₁₀O forms 2,4-DNP derivative, does not reduce Tollens' reagent but gives positive iodoform test on heating with I₂ in the presence of NaOH. Compound 'X' gives ethanoic acid and propanoic acid on vigorous oxidation. Write the (i) Structure of the compound 'X'. (ii) Structure of the product obtained when compound 'X' reacts with 2,4-DNP reagent. (iii) Structures of the products obtained when compound 'X' is heated with I₂ in the presence of NaOH.

Addition of Ammonia Derivatives to Carbonyl Compounds, Oxidation of Aldehydes and Ketones, Tests for Aldehydes and Ketones | PadhAiPro

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TextAddition of Ammonia Derivatives to Carbonyl CompoundsOxidation of Aldehydes and KetonesTests for Aldehydes and KetonesCBSE PYQ

Oxidation of propanal is easier than propanone. Why ?

How can you distinguish between Acetophenone and Benzophenone ?

TextAddition of Ammonia Derivatives to Carbonyl CompoundsOxidation of Aldehydes and KetonesTests for Aldehydes and Ketones

Draw the structure of the following derivative : 2,4-Dinitrophenylhydrazone of Propanone

Which acid of the following pair would you expect to be stronger ? F-CH₂-COOH or CH₃-COOH

Arrange the following compounds in increasing order of their boiling points : CH₃CH₂OH, CH₃-CHO, CH₃-COOH

Give simple chemical test to distinguish between Benzaldehyde and Acetophenone.