Potential energy can be calculated by the formula Pe=mgh. Plug in your values:
Pe=mgh
Pe=(6 kg)(9.8m/s^2)(100 m)
Pe=5880 kg x m^2/s^2, or 5880 Joules
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.
The effective nuclear charge is an innate property of a specific element. It is the pull of force that an electron feels from the nucleus. It is related to the valence electron by the equation: Z* = Z-S, where Z* is the effective nuclear charge, Z is the atomic number and S is the shielding constant.
For the following elements in the choices, these are their values of Z*:
Aluminum - +12.591
Beryllium - +1.912
Hydrogen - +1
Carbon - +4
The effective nuclear charge of Boron is +3. Thus, the answers are Aluminum and Carbon.