enting Appoint... Opportunity Queue WHY? RC RRL EGoogle Docs m Elms College Genetics 1,3-Cyclopentadiene (pKa = 16) is a much stronger acid than cyclopentane (pka = 44). WS02 e Blackboard Uhart Select one: O A. The pi electrons of 1,3-cyclopentadiene repel a hydrogen ion away from the molecule O B. The conjugate base of 1,3-cyclopentadiene is a stable, aromatic species, while the conjugate base of cyclopentane is not aromatic and is much less stable. O C. The shorter C-C bonds of 1,3-cyclopentadiene greatly augment its acid strength. COD. Steric effects render 1,3-cyclopentadiene a stronger acid. OE. 1,3-cyclopentadiene (the acid) has resonance stability; cyclopentane does not. US 0 Mar 16 6:26 8
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RC RRL
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m Elms College
Genetics
1,3-Cyclopentadiene (pKa = 16) is a much stronger acid than cyclopentane (pka = 44).
WS02
9
Blackboard Uhart
Select one:
O A. The pi electrons of 1,3-cyclopentadiene repel a hydrogen ion away from the
molecule
O B. The conjugate base of 1,3-cyclopentadiene is a stable, aromatic species, while the
conjugate base of cyclopentane is not aromatic and is much less stable.
O C.
The shorter C-C bonds of 1,3-cyclopentadiene greatly augment its acid strength.
Steric effects render 1,3-cyclopentadiene a stronger acid.
COD.
O E. 1,3-cyclopentadiene (the acid) has resonance stability; cyclopentane does not.
US
g Mar 16 6:26 8](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5e9dc498-be4a-410d-8f34-ff75919de7f8%2F4def2003-9374-4258-8a40-6719a4ee226a%2Fyhjupe_processed.jpeg&w=3840&q=75)
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