Question

Provide a detailed forward synthesis for the following molecules.

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Answer 1

Anas ose molende Sunthesis poz @ O HNOZA Mayo 4 Nitahon B02 Brucene AB12 2 Br. Nitrobrazor Toyhaumo altro benzor Bestrup Tractor with glitois arid of Suphiae arrd to gives ni nobesuere then seart homine to give in- brumo sito broarne NO) is deactivatus ( meta directing) No2 T . Sn/HCl, H 2 CH32 NHL They reduced by sn/Hel to give amine. amines are highly active so then converted into whakly deathed bactivator by using arelyl chloride NHL Lan honen Noz NHL weakly activatos so nitrason al para position second molewe take place In this case stashing material two functional group kenne & ester ketone ) more reactive than ester that way first they are posterted by using methanol meon HO Popmeout Shoe meor, het meoy me one. ome on ome for goigsrodt regeot mo - ame ome First Form ketal then react with griqaod reagent to forget molerwe.