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Although aldehydes are easily oxidisable...

Although aldehydes are easily oxidisable, propanal can conveniently be prepared by oxidation of propanol by acidified potassium dichromate. Why ?

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The aldehydes can be conveniently oxidised to their respective acids only if they are not removed from the reaction mixture during preparation. As the boiling point of propanal is low (323K), it is conveniently distilled out during the reaction. This avoids its further oxidation.
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Carbonyl compounds give different oxidation products with different reagents .Several oxidising agents can be used to oxidise carbonyy compounds .Ammonical silver nitate (tollens reagent ) oxidises aliphatic as well as aromatic aldehydes . R-CHO overset("Tollens reagents ") to R-COOh +Ag (silver mirror ) strong oxidatising agents like KMnO_4 //H^+ ,HNO_3 ,K_2 Cr_2 O_7 //H^+ oxidise Aldehydes as well as ketons . open chain ketons in oxidation give mixture of two carbonylic acids . oxidation as well as ketons of unsymmetrical ketons takes place according to popoff's rule .According to this rule alpha - carbon whose bond breaks in oxidation always belongs to the alkyl group which has more number of carbons the reagent which oxidise only aliphatic ketone is :

Carbonyl compounds give different oxidation products with different reagents .Several oxidising agents can be used to oxidise carbonyy compounds .Ammonical silver nitate (tollens reagent ) oxidises aliphatic as well as aromatic aldehydes . R-CHO overset("Tollens reagents ") to R-COOh +Ag (silver mirror ) strong oxidatising agents like KMnO_4 //H^+ ,HNO_3 ,K_2 Cr_2 O_7 //H^+ oxidise Aldehydes as well as ketons . open chain ketons in oxidation give mixture of two carbonylic acids . oxidation as well as ketons of unsymmetrical ketons takes place according to popoff's rule .According to this rule alpha - carbon whose bond breaks in oxidation always belongs to the alkyl group which has more number of carbons which of the following is most reactive towards oxidation ?

Carbonyl compounds give different oxidation products with different reagents .Several oxidising agents can be used to oxidise carbonyy compounds .Ammonical silver nitate (tollens reagent ) oxidises aliphatic as well as aromatic aldehydes . R-CHO overset("Tollens reagents ") to R-COOh +Ag (silver mirror ) strong oxidatising agents like KMnO_4 //H^+ ,HNO_3 ,K_2 Cr_2 O_7 //H^+ oxidise Aldehydes as well as ketons . open chain ketons in oxidation give mixture of two carbonylic acids . oxidation as well as ketons of unsymmetrical ketons takes place according to popoff's rule .According to this rule alpha - carbon whose bond breaks in oxidation always belongs to the alkyl group which has more number of carbons 2 methyl cyclohexanone in oxidation wil give

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