Why does cyclohexanol have a pK, of 18 and phenol, despite its similarities in structure, have a pK, of 10? Phenol has a resonance-stabilized conjugate base, which increases the stability of the base and favors its formation Cycohexanol has a resonance-stabilized structure, which increases its stability and reduces the likelihood that it will react to form a conjugate base Phenol has a resonance-stabilized conjugate base, which decreases the stability of the base and inhibits its formation Cycohexanol has a resonance-stabilized conjugate base, which increases the stability of the base and favors its formation Phenol has a resonance-stabilized conjugate base, which decreases the stability of the base and favors its formation
Why does cyclohexanol have a pK, of 18 and phenol, despite its similarities in structure, have a pK, of 10? Phenol has a resonance-stabilized conjugate base, which increases the stability of the base and favors its formation Cycohexanol has a resonance-stabilized structure, which increases its stability and reduces the likelihood that it will react to form a conjugate base Phenol has a resonance-stabilized conjugate base, which decreases the stability of the base and inhibits its formation Cycohexanol has a resonance-stabilized conjugate base, which increases the stability of the base and favors its formation Phenol has a resonance-stabilized conjugate base, which decreases the stability of the base and favors its formation
Chemistry
10th Edition
ISBN:9781305957404
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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![Why does cyclohexanol have a pK, of 18 and phenol, despite its similarities
in structure, have a pK, of 10?
Phenol has a resonance-stabilized conjugate base, which increases the stability of
the base and favors its formation
Cycohexanol has a resonance-stabilized structure, which increases its stability and
reduces the likelihood that it will react to form a conjugate base
Phenol has a resonance-stabilized conjugate base, which decreases the stability of
the base and inhibits its formation
Cycohexanol has a resonance-stabilized conjugate base, which increases the
stability of the base and favors its formation
Phenol has a resonance-stabilized conjugate base, which decreases the stability of
the base and favors its formation](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd2c31123-b150-4f1b-a064-ec93c422882e%2Ff77ba744-45d2-4cac-9a3a-e10eb57e014c%2Fwfj32c_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Why does cyclohexanol have a pK, of 18 and phenol, despite its similarities
in structure, have a pK, of 10?
Phenol has a resonance-stabilized conjugate base, which increases the stability of
the base and favors its formation
Cycohexanol has a resonance-stabilized structure, which increases its stability and
reduces the likelihood that it will react to form a conjugate base
Phenol has a resonance-stabilized conjugate base, which decreases the stability of
the base and inhibits its formation
Cycohexanol has a resonance-stabilized conjugate base, which increases the
stability of the base and favors its formation
Phenol has a resonance-stabilized conjugate base, which decreases the stability of
the base and favors its formation
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