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.
Alkenes on reaction with meta-chloroperoxybenzoic acid (MCPBA ) produces epoxides. When styrene is reacted with mCPBA it gives 2-phenyloxirane as shown below,
Yes and no because it's important for a citizen to have a grasp on chemistry but you do not need it to be a politician
Answer is: Ksp for silver sulfide is 8.00·10⁻⁴⁸.
Reaction
of dissociation: Ag₂S(s) → 2Ag⁺(aq) + S²⁻(aq)<span>.
</span>s(Ag₂S) = s(S²⁻) = 1.26·10⁻¹⁶ M.
s(Ag⁺) = 2s(Ag₂S) = 2.52·10⁻¹⁶ M; equilibrium concentration of silver cations.
Ksp = s(Ag⁺)² · s(S²⁻).
Ksp = (2.52·10⁻¹⁶ M)² · 1.26·10⁻¹⁶ M.
Ksp = 6.35·10⁻³² M² · 1.26·10⁻¹⁶ M.
Ksp = 8.00·10⁻⁴⁸ M³.
Should be :
Lead Sulfate Tetrahydrate