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- Draw all products formed by treatment of each dibromide (A and B) with one equivalent of NaNH2Rank the species in each group in order of increasing nucleophilicity.a. CH3CH2S-, CH3CH2O-, CH3CO2- in CH3OHb. CH3NH2, CH3SH, CH3OH in acetonec. -OH, F-, Cl- in acetoned. HS-, F-, Cl- in CH3OHWhich compound reacts fastest in an E1 rxn. The correct answer is C but explain why it is correct and why the other options are incorrect. thanks :)
- Using chair confirmations, draw the final product of each molecule. Pls explain how are you arrived at the answerthank you!If H+ is eliminated from the compound below, three different products can be formed. Draw the three products.Draw the products formed when each dihalide is treated with excess NaNH2.