How do i answer these retrosynthesis question, showing the synthons, etc. I understand that $1)$ can be performed using Gabriel Amine synthesis $($which i was taught$),$ but how do i show it$?$ What about $2)$ show mechanisms for $1)$ and $2)$ so i can understand the logic of the reactions

Transcribed Image Text:

1) Proposed a synthesis of 2) Proposed a synthesis of NH NH starting from starting from 1) Proposed a synthesis of 2) Proposed a synthesis of NH NH starting from starting from

Answer rating: 100% (QA)

In retrosynthetic analysis you work backwards from the target molecule to simpler precursors This process involves identifying strategic bonds to disconnect in order to propose a viable synthetic path... View the full answer