Question

the What is write it's mechanism of the below reaction ? Also final product. сиз Et -NH₂ NaOH И.0, Д By

Answer 1

​​​​​​Mechanism proceed through E2 and is shown in the reaction above.

E CH₂ Nach Alkene Mi By 429, A A Naoll → strong bone 20 polar brotic There que favorable conditions fol Elimination re theionyl /E 2 mechanism The B-hydrogen As lemoned using bare followed subsequent lemoval of halogen produces Alkene and the leaction is called as ß-elimination veaction, for B-Elimination rx, thacryle E2 mechanising Anti-periplancuity is ette needed olientation, Coverleppry of - obitals is good in Anti-peveplanar arrangement]. Rotatate at HNACH₃ Cl3 H EM this colon NH₂ 4N CH₂ H H rotalt B > at this carbon Вх CLH n.84 → Rotated for prosenting Boe on i plane & showing anti-periplanavity for better understanding, -> Rotating all the thosce bonds does not alter thu Confiplasthani Ans: Z-dikene NH Н Zalkene. * PLZ RATE TMS to

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