323672
An organic compound of molecular formula \(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\) did not give a silver mirror with Tollens' reagent, but gave an oxime with hydroxylamine, it may be
(1) Organic compound gave an oxime with hydroxylamine, therefore, it must be an aldehyde or ketone. (2) Organic compound did not give silver mirror with Tollens' reagent, therefore, it cannot be an aldehyde. Therefore, compound is ketone and its molecular formula will be \(\mathrm{CH}_{3} \mathrm{COCH}_{3}\).
When aldehydes are treated with Tollen's reagent (ammoniacal solution of silver nitrate), these are oxidised to carboxylate ion while Tollen's reagent reduces to metallic silver which gives a shiny appearence of silver mirror.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323674
Tollen's reagent can be obtained by mixing aqueous \(\mathrm{AgNO}_{3}\) with aqueous \(\mathrm{NH}_{3}\) solution. The reagent mainly contains
323672
An organic compound of molecular formula \(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\) did not give a silver mirror with Tollens' reagent, but gave an oxime with hydroxylamine, it may be
(1) Organic compound gave an oxime with hydroxylamine, therefore, it must be an aldehyde or ketone. (2) Organic compound did not give silver mirror with Tollens' reagent, therefore, it cannot be an aldehyde. Therefore, compound is ketone and its molecular formula will be \(\mathrm{CH}_{3} \mathrm{COCH}_{3}\).
When aldehydes are treated with Tollen's reagent (ammoniacal solution of silver nitrate), these are oxidised to carboxylate ion while Tollen's reagent reduces to metallic silver which gives a shiny appearence of silver mirror.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323674
Tollen's reagent can be obtained by mixing aqueous \(\mathrm{AgNO}_{3}\) with aqueous \(\mathrm{NH}_{3}\) solution. The reagent mainly contains
323672
An organic compound of molecular formula \(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\) did not give a silver mirror with Tollens' reagent, but gave an oxime with hydroxylamine, it may be
(1) Organic compound gave an oxime with hydroxylamine, therefore, it must be an aldehyde or ketone. (2) Organic compound did not give silver mirror with Tollens' reagent, therefore, it cannot be an aldehyde. Therefore, compound is ketone and its molecular formula will be \(\mathrm{CH}_{3} \mathrm{COCH}_{3}\).
When aldehydes are treated with Tollen's reagent (ammoniacal solution of silver nitrate), these are oxidised to carboxylate ion while Tollen's reagent reduces to metallic silver which gives a shiny appearence of silver mirror.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323674
Tollen's reagent can be obtained by mixing aqueous \(\mathrm{AgNO}_{3}\) with aqueous \(\mathrm{NH}_{3}\) solution. The reagent mainly contains
323672
An organic compound of molecular formula \(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\) did not give a silver mirror with Tollens' reagent, but gave an oxime with hydroxylamine, it may be
(1) Organic compound gave an oxime with hydroxylamine, therefore, it must be an aldehyde or ketone. (2) Organic compound did not give silver mirror with Tollens' reagent, therefore, it cannot be an aldehyde. Therefore, compound is ketone and its molecular formula will be \(\mathrm{CH}_{3} \mathrm{COCH}_{3}\).
When aldehydes are treated with Tollen's reagent (ammoniacal solution of silver nitrate), these are oxidised to carboxylate ion while Tollen's reagent reduces to metallic silver which gives a shiny appearence of silver mirror.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323674
Tollen's reagent can be obtained by mixing aqueous \(\mathrm{AgNO}_{3}\) with aqueous \(\mathrm{NH}_{3}\) solution. The reagent mainly contains
323672
An organic compound of molecular formula \(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\) did not give a silver mirror with Tollens' reagent, but gave an oxime with hydroxylamine, it may be
(1) Organic compound gave an oxime with hydroxylamine, therefore, it must be an aldehyde or ketone. (2) Organic compound did not give silver mirror with Tollens' reagent, therefore, it cannot be an aldehyde. Therefore, compound is ketone and its molecular formula will be \(\mathrm{CH}_{3} \mathrm{COCH}_{3}\).
When aldehydes are treated with Tollen's reagent (ammoniacal solution of silver nitrate), these are oxidised to carboxylate ion while Tollen's reagent reduces to metallic silver which gives a shiny appearence of silver mirror.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS
323674
Tollen's reagent can be obtained by mixing aqueous \(\mathrm{AgNO}_{3}\) with aqueous \(\mathrm{NH}_{3}\) solution. The reagent mainly contains
