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- 3. (10 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. (C6H5)3P= C- o-C2H5Mechanism. Draw complete arrow-pushing mechanisms for the following reactions.(5 points) Identify the electrophile and the nucleophile in each of the following reaction steps and then draw curved arrows to illustrate the bond-making and bond-breaking processes. C'H;CH CH, + Н-Br CНCH -СH + Br
- Using ChemDraw Draw a mechanism of a reversible reaction of acetophenone and strong acid (H-A) to form a protonated acetophenone and a weak base. Draw all the electron pairs of the molecules and the arrows.37. Propose a synthesis for the target compound, beginning from the starting compound shown. You may use any reagents that you wish. Show all synthetic intermediates and reagents. (5 points) ? HNNone
- Q2-) Draw a detailed mechanism for the following Fischer esterification reaction.(13 points) A few drops of HSO4 Acetic acid Ethanol Ethyl acetate3. a. b. Draw a mechanism for the following reactions. Br 'Br OH- x Br OH Br6. (0.6 pt) Draw the mechanism using the appropriate arrows for the following reaction. OH H2SO4 + H₂O
- 3) Acid catalyzed mechanism a. Draw the mechanism for the following reaction. b. Draw the mechanism of the reverse reaction, also using acid. LOH HO H₂SO4[4.6 pts] Draw the mechanism for the reaction listed below. لي acetone benzaldehyde NaOHPart a) Draw H. Part b) Arrow pushing mechanism from Cyclohexanone to H. Then arrow pushing from H to the product on far right.