Rations Rationalize the major product of the Reaction based upon the Reaction mechanism. your answer should...
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...
4. Answer the following questions based on the electrophilic aromatic substitution reaction shown below. door a. (2.5pts) Based on the identity of the substituent on the starting material and its interaction with the aromatic ring, is this substituent an activator or deactivator? Briefly explain your answer and support your answer with structures b. (5.5pts) Draw all of the resonance contributors of the o-complexes that lead to each of the three possible products. c. (0.5p) Based on the structures drawn in...
Provide the full arrow-pushing mechanism and the major product for the following reaction. Also supply the 3 Sigma Complex Resonance structures in your mechanism:
Draw the major product and write the complete mechanism for the following reaction. Show resonance structures that lead to the formation of the major product.
1. Suggest a reasonable mechanism for the following reaction mage. i.EtON, EtOH, 25°C ii. Hz0 Answer: 2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
1. Suggest a reasonable mechanism for the following reaction. nagogo i.EtON, EtOH, 25°C ii. H,0 Answer: 2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale Answer:
I need help answering this problem Give the final product and the mechanism, with all major resonance structures, for the following reaction: (upload your answer) NO H-O-H 0: + NO 30: Intermediate Upload Choose a File
8. Draw the structure of the major product afforded from the reaction conditions below in the box provided. (5 pts.) Ph3P: CBr4 OH 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 hy p-methyltoluene CI:
6. Propose a mechanism and predict the product for the following reaction. Be sure to include resonance structures. (10 points) OCH AICI, 10 7. Provide the products for the following reactions (12 points) Bra. fuming FeBry H2SO4 AICI
1. Based upon the results obtained in your experiment, formulate a mechanism that will account for all products observed. What rule does the mix follow? 2. One student refluxed the reaction mixture for 20 minutes instead of just distilling over the product as it is formed. The resultant product was approximately 100% 1-methylcyclohexene. Explain why this happened. 3. The GC depicted in Fig. 1 was obtained on analysis of the dehydration of the alcohol below. Interpret the GC data in...