2. (10 points). Using pushing arrows draw stepwise mechanism for the following transformation 90%
3. provide a detailed stepwise mechanism for the following transformation. use curved arrows to show the movement of electrons. (level- mechanism master) 3. Provide a detailed, stepwise mechanism for the following transformation. Use curved arrows to show the movement of electrons. (LEVEL-Mechanism Master) non lo Me 10 nsloo le O mCPBA Me Y ОН OH
7. MECHANISM Using electron push arrows, provide a logical, detailed, stepwise mechanism for the following transformation. Be sure to show each step in the mechanism, including initiation, and propagation steps as well as at least one termination step. HBr → Br ROOR
4) Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for every step, writing statements like "proton transfer without showing the arrows for that step is not an acceptable answer NOE, EIH
8. Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for every step, writing statements like “proton transfer” without showing the arrows for that step is not an acceptable answer. 1. NaOEt, EtOH لا ملہ ان ام Et 2. Hz0+, Heat
Draw a stepwise mechanism for the following transformation:
what's the mechanism? 3. Provide a detailed, stepwise mechanism for the following transformation. Use curved arrows to show the movement of electrons. (LEVEL-Mechanism Master) OH
Mechanism +1 (10 pts). Draw a stepwise mechanism to account for the following transformation. SN/WB OH H2O | || HSO,
2. Draw a detailed arrow pushing mechanism for the following transformation (3 points): i 1)^_MGBT OH H2) H20
explain the mechanism in words c Draw the full electron-pushing mechanism (using proper electron-pushing arrows, intermediates, and structures) for the synthesis of phenolphthalein from phenol and phthalic anhydride. It's an electrophilic aromatic substitution reaction! c Draw the full electron-pushing mechanism (using proper electron-pushing arrows, intermediates, and structures) for the synthesis of phenolphthalein from phenol and phthalic anhydride. It's an electrophilic aromatic substitution reaction!
6. Provide a detailed, stepwise mechanism for the following transformation. Use curved arrows to show the movement of electrons. ...OH ..OH 1. Oz then SMez 2. NaBH4 . MeOH 3. TsOH Meo