Formation of oximes and hydrazones | Aldehydes and ketones | Organic chemistry | Khan Academy

[@pawinnful]

Thank you very much for updating this vdo clip

[@janetundekelleher1321]

Could someone please explain why Brady's reagent + cyclohexanone would not also form an enamine product where the central, secondary amine attacks the alpha carbon. My two guesses would be sterics and/or E withdrawing effects of the ring, but is there another reason? thank you!

[@sheoransavoy4676]

Improve sound quality please and vedio is very nice

[@prasadkelam7302]

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