Question

1. The synthesis of N-benzyl-2-azanorbornene is done through a [4+2] Diels-Alder reaction. NH3C1 CH20 DNH H2O Ph

provide the mechanisme of this reaction!
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Answer #1

diene reacts with dienophile and forms the cyclic adduct - diels alder reaction , here first generate dienophile and then predict the product as follows
Mechance fut It Hall - par atkel I-CI of Hadh pha NH2 | HP protonation 1 Nucleophilic Attack Hach Ha H- C -0 H2 <H20 Hoe oh H

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provide the mechanisme of this reaction! thanks 1. The synthesis of N-benzyl-2-azanorbornene is done through a [...
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