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Draw the product obtained when trans-2-butene is treated first with br2 in ch2cl2, second with nanh2 in nh3, and then finally with h2/lindlar's catalyst.

Respuesta :

shinmin

In order to do this, you have change the alkene into an alkyne. That is the aim of Br2/CH2Cl2 trailed by NaNH2. The Br2 with form a vic dihalide (3,4-dibromo octane). Adding of NaNH2 will execute two E2 reactions. -NH2 will eliminate an H from carbons 3 and 4. This double elimination will make the alkyne. Then handling the alkyne with H2/Lindlar will form the cis alkene. The final product will be CIS-3-octene.