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Date: 24-1-2020
849
Date: 2-12-2019
898
Date: 29-7-2018
2192
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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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هل يمكن للدماغ البشري التنبؤ بالمستقبل أثناء النوم؟
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علماء: طول الأيام على الأرض يزداد بسبب النواة الداخلية
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المجمع العلمي يشرك طلبة الدورات الصيفية بمحفلٍ قرآني في محافظة بابل
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