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4. Provide a plausible mechanism for the reaction shown. (6 pts) 7 NaNH. Hycor ND 5....
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp? hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Dec 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 3. Rank the reactivity of the compounds...
Can you please answer all of them? Section B: Free Response (you must show your work...
Can you please answer all of them?
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Antanan ENon ordre Energy Bunding aromatic antiaromatic 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) nonovomatic...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3 pts)
2. What is the Hückel number of pi electrons for the molecule shown below? How many...
2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 16 Te 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sn2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts)
2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pas does it have? W...
2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pas does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatie? Explain. (3 pts) Rank the reactivity of the compounds shown below when using a Friedel Crafts alkylation fac Make sure you label which is least reactive and most reactive. (5 pts)
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle...
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are spa hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or...
4. Provide a plausible mechanism for the reaction shown. (6 pts) Naal 5. Each transformation shown...
4. Provide a plausible mechanism for the reaction shown. (6 pts) Naal 5. Each transformation shown below requires at least two steps. Provide the reagents/conditions for each transformation. (20 pts) Reng Remsc 6. Predict the products from the Birch reductions shown below. (3 pts) Mì, NHÀ са он Bonus: (6 pts) Provide a synthesis for the target molecule using benzene. CO2H oto сон TM
4. Provide a plausible mechanism for the reaction shown. (6 pts) NaNH . NHA 5. Each...
4. Provide a plausible mechanism for the reaction shown. (6 pts) NaNH . NHA 5. Each transformation shown below re transformation. (20 pts) two steps. Provide the reagents/conditions for each
12. Identify which ammonium ion has the lower pka. Use aromaticity concepts to explain your answers.(3pts)...
12. Identify which ammonium ion has the lower pka. Use aromaticity concepts to explain your answers.(3pts) 13. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 14. The rate of solvolysis of iodide 1 is 100 times faster than the rate of solvolysis of iodide 3. What explanation (with structures) can you provide for...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp? hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Dec 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 3. Rank the reactivity of the compounds...
Can you please answer all of them?
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Antanan ENon ordre Energy Bunding aromatic antiaromatic 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) nonovomatic...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3 pts)
2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 16 Te 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sn2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts)
2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pas does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatie? Explain. (3 pts) Rank the reactivity of the compounds shown below when using a Friedel Crafts alkylation fac Make sure you label which is least reactive and most reactive. (5 pts)
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are spa hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or...
4. Provide a plausible mechanism for the reaction shown. (6 pts) Naal 5. Each transformation shown below requires at least two steps. Provide the reagents/conditions for each transformation. (20 pts) Reng Remsc 6. Predict the products from the Birch reductions shown below. (3 pts) Mì, NHÀ са он Bonus: (6 pts) Provide a synthesis for the target molecule using benzene. CO2H oto сон TM
4. Provide a plausible mechanism for the reaction shown. (6 pts) NaNH . NHA 5. Each transformation shown below re transformation. (20 pts) two steps. Provide the reagents/conditions for each
12. Identify which ammonium ion has the lower pka. Use aromaticity concepts to explain your answers.(3pts) 13. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 14. The rate of solvolysis of iodide 1 is 100 times faster than the rate of solvolysis of iodide 3. What explanation (with structures) can you provide for...
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