Answer:
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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:
Part A. The half-cell B is the cathode and the half-cell A is the anode
Part B. 0.017V
Explanation:
Part A
The electrons must go from the anode to the cathode. At the anode oxidation takes place, and at the cathode a reduction, so the flow of electrons must go from the less concentrated solution to the most one (at oxidation the concentration intends to increase, and at the reduction, the concentration intends to decrease).
So, the half-cell B is the cathode and the half-cell A is the anode.
Part B
By the Nersnt equation:
E°cell = E° - (0.0592/n)*log[anode]/[cathode]
Where n is the number of electrons being changed in the reaction, in this case, n = 2 (Sn goes from S⁺²). Because the half-reactions are the same, the reduction potential of the anode is equal to the cathode, and E° = 0 V.
E°cell = 0 - (0.0592/2)*log(0.23/0.87)
E°cell = 0.017V
Answer:
B
Explanation:
the electrical charges of nonpolar molecules are evenly distributed across the molecule