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

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

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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