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- Please don't provide hand written solution....2- Write step-by-step mechanism for the following reaction: Cul R1 но .*...... ....... ........Bu Br ML. से 1) 1.05 nBuLi 2) A) -78 30 min MeOH B-78 to RT for 1h; MeOH e Bu H what would be the mechanism/interaction between the n-Butyllithium and the starting material to get to the product? Please explain step by step.
- (Please step by step solutions) Can you do the mechanism?! ( plz ans with proper explanation , aslo give mechanism. For the following reaction: Br to Na -OH + ? a. identify the type of alkyl halide: b. identify the type of nucleophile/base: c. predict the anticipated mechanism(s): d. predict the major organic product by drawing the appropriate mechanism: . For the following reaction: Br -OH ? a. identify the type of alkyl halide: b. identify the type of nucleophile/base: c. predict the anticipated mechanism(s): d. predict the major elimination product by drawing the appropriate mechanism:
- 08:12 r ||| 3. The final product is removed from the organic layer by extraction with the hydrochloric acid solution. Draw the curved arrows for the proton transfer reaction that takes place, and draw the resulting product. Explain how this reaction enables the removal of the lidocaine from the organic layers. dr organic layer by extraction proton transfer reaction the on enables the removal of of th H-C < O <3 H-CI pan 3 and pat C of the i. || | PeterPredict the product for the following reaction sequence. 2-methyl-1-propanol PBr3 OH Br || Ja fla OH V IV O Br Mg/ether ||| 1. CO₂ 2. H3O+ OHPredict the product(s) of the acid/base reactions below. Draw curved arrows to show the formation and breaking of bonds.