Current Attempt in Progress HO meta-Hydroxyacetophenone para-Hydroxyacetophenone The conjugate base of the para isomer has a negative charge that is delocalized over atom(s), and the conjugate base of the meta (somer has a negative charge that is delocalized over oxygen atom(s). Therefore, the conjugate base of the meta isomer is making meta-hydroxyacetophenone acidic than para-hydroxyacetophenone. carbon atom(s) and oxygen carbon atom(s) and stable than then conjugate base of the para isomer,

Chemistry
10th Edition
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Current Attempt in Progress
HO
De or
HO
meta-Hydroxyacetophenone
para-Hydroxyacetophenone
The conjugate base of the para isomer has a negative charge that is delocalized over
atom(s), and the conjugate base of the meta isomer has a negative charge that is delocalized over
oxygen atom(s). Therefore, the conjugate base of the meta isomer is
making meta-hydroxyacetophenone
carbon atom(s) and
acidic than para-hydroxyacetophenone
oxygen
carbon atom(s) and
stable than then conjugate base of the para isomer,
Transcribed Image Text:Current Attempt in Progress HO De or HO meta-Hydroxyacetophenone para-Hydroxyacetophenone The conjugate base of the para isomer has a negative charge that is delocalized over atom(s), and the conjugate base of the meta isomer has a negative charge that is delocalized over oxygen atom(s). Therefore, the conjugate base of the meta isomer is making meta-hydroxyacetophenone carbon atom(s) and acidic than para-hydroxyacetophenone oxygen carbon atom(s) and stable than then conjugate base of the para isomer,
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