A ketone A (C4H8O) which undergoes Iodoform reaction gives compound B on reduction. B on heating with conc.H2SO4 at 443 K gives a compound C which forms ozonide D. D on hydrolysis with Zn dust gives only E. Identify the compounds A to E. Write the Iodoform reaction with compound A.

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Dehydration of Alcohols, Reduction of Aldehydes and Ketones, Tests for Aldehydes and Ketones | PadhAiPro

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TextDehydration of AlcoholsReduction of Aldehydes and KetonesTests 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

Write the main product in the following reactions :

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