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
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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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:Erling 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
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
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