For the following reaction predict the major product and draw the complete mechanism including the mechanism for the electrophile formation. CF3 H₂SO4 HNO3
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- Draw the favored product(s) of the following reactions (organic chemistry)Identify the major product of the following reaction sequence. 1) [H*], H₂NNH2, (-H₂O) 2) KOH/H₂O, heat HO₂C HO₂C HO CO,H OH OH There is no reaction under these conditions or the correct product is not listed here.Predict the major product of the reaction and draw it in the space provided. + HN. NPh NaBH3CN MeOH/ACOH
- Draw the mechanism for the following reaction and identify the major reaction product. (1) NaBH4 (2) H3O+Which of the following reactions would result in the correct product?Br Brz CH3 CH3 H3C CH2CI2 H3C Br Electrophilic addition of bromine, Br2; to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH,Cl). In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br: :Br: .CH3 H3C H3C CH3 Br:
- Complete the following reaction with mechanism and a major product: O₂N- -CHCO₂Et CO₂Et PhCH₂Cl K₂CO3In the presence of light or heat, diazomethane (CH,N2) creates a carbene, which then adds to an alkene to make a cyclopropane. In the boxes below. draw the mechanism arrows for the reaction. H INEN: INE N:Consider the following reaction scheme (note that the reagent shown above the arrow is DBN"). Draw in the expected major product AND indicate what mechanism the reaction will follow. Product: Mechanism: