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Consider imidazole (far right): a. Draw a Frost circle diagram for imidazole. (1 pt) b. Label...
4. Consider imidazole (far right): a. Draw a Frost circle diagram for imidazole. (1 pt) b....
4. Consider imidazole (far right): a. Draw a Frost circle diagram for imidazole. (1 pt) b. Label the MOs as "bonding." "anti-bonding." or "non-bonding" (if applicable). (1 pt) c. Fill in imidazole's conjugated pl-system electrons on the Frost diagram. (1 pt) d. Would you expect imidazole to be aromatic or antiaromatic? (1 pt) Explain how your Frost circle results support your answer. (1 pt) imidazole
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...
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)
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...
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. (12 pt) Complete the following a. The following molecules is (circle or The number of...
1. (12 pt) Complete the following a. The following molecules is (circle or The number of pi electrons in the pi system is following molecules is (circle one): aromatic, anti-aromatic, non-aromatic. b. The following molecules is (circle one): aromatic, anti-aromatic, non-aromatic. The total number of p orbitals in the molecule is . Only p orbitals are included in the pi system. c. Caffeine is: (circle one) aromatic, anti-aromatic How many p orbitals are in the pi system? Circle all the...
Antibonding MOS 3. The energy diagram (right) depicts the molecular orbitals for the pi electrons in...
Antibonding MOS 3. The energy diagram (right) depicts the molecular orbitals for the pi electrons in a molecule with a cyclic, fully-conjugated pi system. Would you expect the molecule to be unusually stable or unusually unstable? Why? Explain in 1-2 sentences. (2 pts) Energy - ----Nonbonding MOs y Bonding MOs
The H2O molecule. a) Sketch the Lewis Dot structure. b) Consider Hybridation of O's AOs. Draw...
The H2O molecule. a) Sketch the Lewis Dot structure. b) Consider Hybridation of O's AOs. Draw the MO diagram that would result, or explain the TWO "H-O bonds." Be sure to label them on your diagram. c) Label the MOs in your diagram. Are they sigma type or pi type interactions ? Bonding or Anti-bonding? d) Let's now consider those other electrons in the molecule. They ( 4 electrons ) are not contributing or disrupting the bonds between H and...
Draw the molecular orbital diagram using the polygon method of cycloheptatriene anion. Label all the orbitals...
Draw the molecular orbital diagram using the polygon method of cycloheptatriene anion. Label all the orbitals and fill in the electrons in the system. Use the molecular orbital diagram to predict whether the system is non, anti, or aromatic and explain your answer without using huckels rule.
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...
4. Consider imidazole (far right): a. Draw a Frost circle diagram for imidazole. (1 pt) b. Label the MOs as "bonding." "anti-bonding." or "non-bonding" (if applicable). (1 pt) c. Fill in imidazole's conjugated pl-system electrons on the Frost diagram. (1 pt) d. Would you expect imidazole to be aromatic or antiaromatic? (1 pt) Explain how your Frost circle results support your answer. (1 pt) imidazole
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...
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)
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...
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. (12 pt) Complete the following a. The following molecules is (circle or The number of pi electrons in the pi system is following molecules is (circle one): aromatic, anti-aromatic, non-aromatic. b. The following molecules is (circle one): aromatic, anti-aromatic, non-aromatic. The total number of p orbitals in the molecule is . Only p orbitals are included in the pi system. c. Caffeine is: (circle one) aromatic, anti-aromatic How many p orbitals are in the pi system? Circle all the...
Antibonding MOS 3. The energy diagram (right) depicts the molecular orbitals for the pi electrons in a molecule with a cyclic, fully-conjugated pi system. Would you expect the molecule to be unusually stable or unusually unstable? Why? Explain in 1-2 sentences. (2 pts) Energy - ----Nonbonding MOs y Bonding MOs
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...
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