Show the mechanism of the synthesis of Omeprazole, include resonance structures and curly arrows.
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
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.
need help with the mechanism must include all steps and show all curly arrows and workings. + Meo, co Me (1) NaOH Naome Ovo (1) HCIO MeOH X CO,Me () heat NB: When writing the mechanism for dimedone formation you need to include all of the following steps (i) the Michael addition, (ii) the Dieckmann condensation, (iii) the hydrolysis of the ester and (iv) the decarboxylation of the B-keto acid
Complete the step-by-step mechanism, including all resonance structures, for the following reaction. Show proper arrows and lone pairs for full credit. NaOH H20 НО
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 ?????
# 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)
write the full step wise mechanism for the reaction with proper charges, arrows and resonance structures and identify the major and minor structures for it. HBr Excess Her
a . Using curly / curved arrows , provide a mechanism for the reaction below : 40 Marks Question 5 a. Using curly/curved arrows, provide a mechanism for the reaction below: CI HCI
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 the mechanism of the following reaction. Be sure to show all curved arrows and formal charges. (Show the formation of the electrophile and all resonance structures of the sigma complex). o to AICI: Does the substituent on the following benzene activate or deactivate the ring for EAS reactions? Explain your answer this should include drawing any relevant resonance structures!) NH Predict the major product of the following reaction. Explain the directing effects of the -OH group (this should include...