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Date: 28-6-2016
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Date: 15-10-2019
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Date: 28-5-2017
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The previous reactions have all involved reagents of the type: Y–NH2, i.e. reactions with a 1º-amino group. Most aldehydes and ketones also react with 2º-amines to give products known as enamines. Two examples of these reactions are presented in the following diagram. It should be noted that, like acetal formation, these are acid-catalyzed reversible reactions in which water is lost. Consequently, enamines are easily converted back to their carbonyl precursors by acid-catalyzed hydrolysis. A mechanism for enamine formation may be seen by pressing the "Show Mechanism" button.
Mechanisim
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"إنقاص الوزن".. مشروب تقليدي قد يتفوق على حقن "أوزيمبيك"
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الصين تحقق اختراقا بطائرة مسيرة مزودة بالذكاء الاصطناعي
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مكتب السيد السيستاني يعزي أهالي الأحساء بوفاة العلامة الشيخ جواد الدندن
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