provide the reaction mechanism of 4-methylaniline reacting with water. include all resonance structures if applicable
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provide the reaction mechanism of 4-methylaniline reacting with water. include all resonance structures if applicable
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 ?????
Provide the product(s) and mechanism for the following reactions. Include all intermediates, resonance structures, charges, and electron pushing arrows to obtain full credit. 1. 2. 3. 4. 1 Ph MgBr 2. Hао 1. сн.MgBr 2. H,о- Et heat Me ОН ??? -ОН
3. (18 pt) Provide a detailed arrow-pushine mechanism for the following reaction. Don't forget resonance structures when applicable. b. The reaction above gives only ortho product. Give two reasons why the para product doesn't form.
Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. (14 points) Pro excess HBr Br
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
5. (15 pt) a. Complete the following reaction. b. Draw a complete mechanism (include resonance structures). c. Explain the directing effect in this case using resonance structures OCH3 H3PO4 OCH3
please provide explannation of the process, thanks. 3) Resonance Structures: Draw all of the resonance structures for the product of the reaction shown and label major and minor resonance forms. H-O H 3) Resonance Structures: Draw all of the resonance structures for the product of the reaction shown and label major and minor resonance forms. H-O H
Provide a full mechanism for the synthesis of 3-acetyl-7-(diethylamino)-2H-1-benzopyran-2-one. Include all formal charges, resonance structures, intermediates and products. Use proper arrows for electron flow, vaguely drawn arrows will not receive marks.
Provide a mechanism for the three resonance structures of arginine at physiological pH.
Show the mechanism of the synthesis of Omeprazole, include resonance structures and curly arrows.