An organic compound [A] having molecular formula C4H10O forms a compound [B] with molecular formula C4H8O on oxidation. Compound [B] gives a positive iodoform test. The reaction of compound [B] with CH3MgBr followed by hydrolysis gives compound [C] with molecular formula C5H12O. Identify the compounds [A], [B] and [C]. Write the reaction for the conversion of compound [A] to compound [B].

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Preparation of Ketones by Oxidation of Alcohols, Addition of Grignard Reagents to Carbonyl Compounds, Tests for Aldehydes and Ketones | PadhAiPro

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TextPreparation of Ketones by Oxidation of AlcoholsAddition of Grignard Reagents to Carbonyl CompoundsTests for Aldehydes and Ketones

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

What happens when

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