Question

Discussion TF cle4 was prepared via treatment of molecule 3 with hydroxyl amine and catalytic acetic acid. Provide and B as your base. (Hint: The last step is similar to an El elimination) BUID: d arrow mechanism for the most straightforward conversion of 3 to 4. You may use HB' your Discussion section: cat 5) Chemists tried to synthesize the amine below via a SN2 mechanism. Explain what would be the actual product they would obtain and why they would obtain it. (Hint: Nucleophilicity of amines: tetriary secondary primary> NH3.) How could they make the desired amine through chemistry you have just learned? Br NH2 desired amine NH3

Answer 1

ADH он 4) echanisn US он о 0越 チH+ 丹 4t βγ Th.hreauti Bw İg, onat dappen beca u-se the Produd is formed it wid att auk an-dthe any ame tent mine