provide all important resonance structure of the following anion, and show the electron pushing arrows from one resonance to another

provide all important resonance structure of the following anion, and show the electron pushing arrows from...
4. Provide a stepwise mechanism. Include all intermediates, resonance structures, and electron pushing arrows.(ALL OR NOTHING) HEC CH3 AICI D. HCI 5. (Provide the product(s) or reagent(s) for the following reactions. COM ????? ON 77277 HON C ?????
1. There are three possible resonance structures of phenoxide; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 2. There are three possible resonance structures of phenyl ethanoate, draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid
Draw reasonable resonance structures. Use electron
pushing arrow notation to show the conversion of a resonance
structure into another structure.
1) Provide a detailed electron pushing mechanism for the below transformation. Show ALL relevant resonance structures to help explain why the para product is the major organic product. (Note: your electron pushing mechanism should include formation of the electrophile) (4 points) Cl AICl3
9. Provide a proper electron-pushing mechanism (including resonance structures) using curved arrows that describes the monochlorination of p-methyltoluene. (10 pts.) CI-CI + HCI hv p-methyltoluene ci
Draw five resonance structures for this radical anion. Please show
the motion of electron pairs and bonds using curved arrows.
O Θ
4) Provide all the Resonance structures of the Cycloheptatrienyl Cation, using arrows show the flow of electrons (delocalization) in each resonance structure. (2 points)
Organic Chemistry
Provide mechanism for reaction while using electron pushing
arrows showing all possible intermediates and include the most
stable resonance.
SbCl5 t-BuCI /t-BuOH CF3 CF3 e:o. :O NH3 reflux NH 2 b) Ci: CO CF3 CF3
# 2 A Draw one resonance structure for the following radical, using curly arrows to illustrate the flow of electrons from one resonance structure to the next (2 pts). b Draw an arrow-pushing mechanism to account for the following reaction (5 pts). HB Draw an arrow pushing mechanism to account for the following reaction. (3 pts)
2. There are three possible resonance structures of phenyl ethanoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid