1. Compare the electron density maps for the two compounds. (They were both created using the same color scale.) There is more electron density around the oxygen in cycloheptatrienone compared to the oxygen in cyclopentadienone. Explain the difference. Cycloheptatrienone Cyclopentadienone 2. One of your labs in CHM2211L uses cyclopentadiene as a reagent in a Diels-Alder reaction. However, before it can be used in that reaction it must be heated and distilled as the compound dimerizes while it is stored. Draw the dimerization reaction in bond line form. 3. Is the following compound aromatic? Detail how it meets or does not meet the qualifications of aromaticity. If it is not aromatic, could it easily be converted into an aromatic compound? How? H CX H

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Chapter1: Chemical Foundations
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1. Compare the electron density maps for the two
compounds. (They were both created using the
same color scale.) There is more electron density
around the oxygen in cycloheptatrienone
compared to the oxygen in cyclopentadienone.
Explain the difference.
Cycloheptatrienone
Cyclopentadienone
2. One of your labs in CHM2211L uses
cyclopentadiene as a reagent in a Diels-Alder
reaction. However, before it can be used in that
reaction it must be heated and distilled as the
compound dimerizes while it is stored. Draw the
dimerization reaction in bond line form.
3. Is the following compound aromatic? Detail how it
meets or does not meet the qualifications of
aromaticity. If it is not aromatic, could it easily be
converted into an aromatic compound? How?
H
CX
H
Transcribed Image Text:1. Compare the electron density maps for the two compounds. (They were both created using the same color scale.) There is more electron density around the oxygen in cycloheptatrienone compared to the oxygen in cyclopentadienone. Explain the difference. Cycloheptatrienone Cyclopentadienone 2. One of your labs in CHM2211L uses cyclopentadiene as a reagent in a Diels-Alder reaction. However, before it can be used in that reaction it must be heated and distilled as the compound dimerizes while it is stored. Draw the dimerization reaction in bond line form. 3. Is the following compound aromatic? Detail how it meets or does not meet the qualifications of aromaticity. If it is not aromatic, could it easily be converted into an aromatic compound? How? H CX H
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