Comparing Minima: Catechol has three primary "in the ring plane" distinguishable stationary point conformations with different relative hydroxyl orientations while hydroquinone has only two. a) Identify and image the structures of all these stationary points. Provide RHF energy (in Hartree) for all these structures at the HF/3-21G level. b) Compare the global minimum energies for catechol and hydroquinone. Explain the potential energy difference between these conformers of catechol and hydroquinone.
Comparing Minima: Catechol has three primary "in the ring plane" distinguishable stationary point conformations with different relative hydroxyl orientations while hydroquinone has only two. a) Identify and image the structures of all these stationary points. Provide RHF energy (in Hartree) for all these structures at the HF/3-21G level. b) Compare the global minimum energies for catechol and hydroquinone. Explain the potential energy difference between these conformers of catechol and hydroquinone.
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Chapter1: Chemical Foundations
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![Comparing Minima: Catechol has three primary "in the ring plane" distinguishable stationary point
conformations with different relative hydroxyl orientations while hydroquinone has only two.
a) Identify and image the structures of all these stationary points. Provide RHF energy (in Hartree)
for all these structures at the HF/3-21G level.
b) Compare the global minimum energies for catechol and hydroquinone. Explain the potential
energy difference between these conformers of catechol and hydroquinone.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F79e2b4b5-0ef7-4524-b990-d6cab87de0d3%2F61814e08-8051-444a-98fa-516e924f9c6b%2Fg19587u_processed.png&w=3840&q=75)
Transcribed Image Text:Comparing Minima: Catechol has three primary "in the ring plane" distinguishable stationary point
conformations with different relative hydroxyl orientations while hydroquinone has only two.
a) Identify and image the structures of all these stationary points. Provide RHF energy (in Hartree)
for all these structures at the HF/3-21G level.
b) Compare the global minimum energies for catechol and hydroquinone. Explain the potential
energy difference between these conformers of catechol and hydroquinone.
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