Exam 8: Delocalized Electrons: Their Effect on Stability, pka, and the Products of a Reaction - Aromaticity and Electronic Effects: an Introduction to the Reactions of Benzene

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The delocalized π system in benzene is formed by a cyclic overlap of 6 ________ orbitals.

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The C-C single bond in the following molecule is formed by the overlap of what type of orbitals? The C-C single bond in the following molecule is formed by the overlap of what type of orbitals?

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Give the major organic product for the reaction. Give the major organic product for the reaction.

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What is the major product obtained from the addition of one mole of HCl at high temperature to 1,3-butadiene?

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Which of the following is aromatic? Which of the following is aromatic?

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What diene and dienophile would react to give the product below? What diene and dienophile would react to give the product below?

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Provide the structure of the major organic product in the following reaction. Provide the structure of the major organic product in the following reaction.

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How would you convert cyclopentadiene to the dialdehyde shown? How would you convert cyclopentadiene to the dialdehyde shown?

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Which π MOs are bonding MOs in the ground state of 1,3,5-hexatriene?

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Why does the (E,E)-isomer of 2,4-hexadiene react much more rapidly with dienophiles than does the (Z,Z)-isomer?

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Provide the structure of the major organic product in the following reaction. Provide the structure of the major organic product in the following reaction.

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Provide the structure of the major organic product in the following reaction. Provide the structure of the major organic product in the following reaction.

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What is/are the product(s)of the following reaction? What is/are the product(s)of the following reaction?

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Indicate the compound that has the shortest bond length between the two middle carbon atoms.

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Indicate whether the following molecule is aromatic,antiaromatic,or nonaromatic. Indicate whether the following molecule is aromatic,antiaromatic,or nonaromatic.

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What is the thermodynamic product for the following reaction? What is the thermodynamic product for the following reaction?

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Which of the following is the weakest acid? Which of the following is the weakest acid?

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What is the product from the following reaction? What is the product from the following reaction?

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Draw the structure of the major product which results when the diene shown is treated with HBr at -80°C. Draw the structure of the major product which results when the diene shown is treated with HBr at -80°C.

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Draw the LUMO of 1,3,5-hexatriene.

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