Answer: it’s b)
Explanation: that’s the only difference that is listed
Answer:
Phenols do not exhibit the same pka values as other alcohols;
They are generally more acidic.
Using the knowledge that hydrogen acidity is directly related to the stability of the anion formed, explain why phenol is more acidic than cyclohexane.
Explanation:
According to Bromsted=Lowry acid-base theory,
an acid is a substance that can release
ions when dissolved in water.
So, acid is a proton donor.
If the conjugate base of an acid is more stable then, that acid is a strong acid.
In the case of phenol,
the phenoxide ion formed is stabilized by resonance.

The resonance in phenoxide ion is shown below:
Whereas in the case of cyclohexanol resonance is not possible.
So, cyclohexanol is a weak acid compared to phenol.
Answer:
The answer is (H30+) =3,55e-8M and (OH-)=2,82e-7M
Explanation:
We use the formulas:
pH= - log(H30+) and Kwater=(H30+)x(OH-)
pH= - log(H30+) ----< (H30+)= antilog- pH=antilog- 7,45=3,55E-8M
Kwater=(H30+)x(OH-)
(OH-)=Kwater/(H30+)= 1,00e-14/3,55e-8 = 2,82e-7
Answer:
i believe lithium dont clown me if im wrong
Explanation: