Explain why the cyclopropenone shown below behaves less as a carbonyl compound than ordinary aliphatic ketones. R Since the following molecule contains an electronegative atom in its structure, it would be expected to possess a dipole moment. Indeed, it does. However, this is much larger than expected, and it is also not oriented in the expected direction. Explain. Furthermore, say with reasons if this molecule would be aromatic or not.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter18: Aromaticity
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Explain why the cyclopropenone shown below behaves less as a
carbonyl compound than ordinary aliphatic ketones.
R
Since the following molecule contains an electronegative atom in its
structure, it would be expected to possess a dipole moment.
Indeed, it does. However, this is much larger than expected, and it
is also not oriented in the expected direction. Explain. Furthermore,
say with reasons if this molecule would be aromatic or not.
Transcribed Image Text:Explain why the cyclopropenone shown below behaves less as a carbonyl compound than ordinary aliphatic ketones. R Since the following molecule contains an electronegative atom in its structure, it would be expected to possess a dipole moment. Indeed, it does. However, this is much larger than expected, and it is also not oriented in the expected direction. Explain. Furthermore, say with reasons if this molecule would be aromatic or not.
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