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How are (1) butanone (2) Pentan-3-one obtained using (i) alcohol and (ii) geminal dihalide? |
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Answer» Solution :(1) Using alcohol: (1) Butan-2-ol on CONTROLLED oxidation with `K_(2)Cr_(2)O_(7)` and dillute `H_(2)SO_(4)` forms butanone. `CH_(3)-UNDERSET("Butan-2-ol") overset(OH)overset(|)(CH)-CH_(2)-CH_(3)+[O]underset("dil". H_(2)SO_(4))overset(K_(2)Cr_(2)O_(7))(to CH_(3)- underset("Butanone")overset(O)overset(||)(CO-CH_(2)-CH_(3)+H_(2)O` (2) Pentan-3-ol on oxidation with `K_(2)Cr_(2)O_(7)` and dilute `H_(2)SO_(4)` forms Pentan-3-one. (2) Using geminal dihalide: (1) When 2, 2-Dichlorobutane is hydrolysed by boiling with aqueous KOH, Butanone is OBTAINED. `CH_(3) - CH_(2)- underset("Butanone")overset(O)overset(||)(C)-CH_(3)+H_(2)O` (2) When 3,3-dichloropentane is hydrolysed by boiling with aqeous `KOH`, Pentan-3-one is obtained. `implies CH_(3)-CH_(2)-underset("Pentan-3-one")overset(O) overset(||)(C-CH_(2))-CH_(3)+H_(2)O` |
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