Provide the product and mechanism for the following reaction.
Provide the product and mechanism for the following reaction. 1. Provide the product and mechanism for...
2. (10 pts) Predict the major product for the following reaction and provide a curved arrow mechanism for the formation of the product 1. NaOH/Br2 2. H30*
PLEASE ANSWER ALL QUESTIONS 41) Provide the major organic product of the following reaction. Bry, FeBry 42) Provide the major organic product that results when benzene is treated with the following sequence of reagents: 1. HNO3, H2SO4 2. Br2, FeBr3. Answer: NO2 43) Explain why Friedel-Crafts alkylation reactions are prone to poly alkylation, whereas Friedel- Crafts acylation reactions are not prone to polyacylation? 44) Which series of reagents would be required to perform the following synthesis? A) 1. CICH2CH2CH3, AICI;...
Provide a mechanism and final product for the following reaction. (6 pts) KCN, EtOH/H0 H CH3 Provide a mechanism for the reaction shown below. (6 pts.) Actones KOHO CH, Part V. Separation, Provide a mechanism and final product for the following reaction. (6 pts) KCN, EtOH/H0 H CH3 Provide a mechanism for the reaction shown below. (6 pts.) Actones KOHO CH, Part V. Separation,
1) Predict the product and provide the mechanism for the following reaction. Your explanation should identify the orbital interactions that occur during this process for full credit. (2 pts) HBr 2) Predict the product and provide the mechanism for the following reaction. Your explanation should identify the orbital interactions that occur during this process for full credit. (3 pts) HCI
1. Provide a reasonable mechanism to account for the following reaction. 3. Propose a reasonable mechanism for the following reactions. 7. Propose a mechanism for the formation of the following products. NO2 H2SO4 HNO; Br Br AICI: + CI Br FeBrz AICI: -CI
1. Predict the product for the following reaction. Provide the mechanism for each reaction. Provide the sterochemistry and regiochemistry where is appropriate. HBr H2O Cat H+ HBr CHEM 2200-Spring 2020 Hydrohalogenation • Markovnikov orientation • Rearrangement can occur 2. Provide the product for the 2. Provide the product for the following reaction. Provide the sterochemistry and regiochemistry where is appropriate. Show the mechanism for C, and D. 0., b) a HC HCI HCI HBT -- "O HCI
Q1 (5 points) 1. Provide the complete mechanism and the final product of the following reaction. reaction. (5 pts) OE NaOE, ETOH
4. (5 pts) Mechanism Show the product(s) of the following reaction, and provide the mechanism and the reaction coordinate diagram. Provide the rate equation for the process HC Nu R CH₂ reaction coordinate Rate Equation Rate =
12. Provide a mechanism and product(s) for the following reaction. Explain the regiochemistry of the product, considering both possible intermediates (i.e. is one pathway preferred over the other, or are they similar in energy?). (10 pts) OH H2SO4
5(a). Predict the product for the following reaction. (b). Provide an arrow-pushing mechanism for the reaction above that accounts for the formation of the product. Explicitly include all non-bonding electrons and charges. Indicate whether each step is an initiation, chain propagation, or termination. (c). An additional product, shown below, is formed in the reaction from part (a). Provide an arrow-pushing mechanism that accounts for the formation of the additional product. (You may start from any intermediate from part (b))....