Answer:
Explanation: Does any of this look right? To be honest I just looked it up.
D NACL because it is ionic bond and all the others are covalent
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.
We know that the equation for density is:

where D is the density, m is the mass in g, and V is the volume in either mL or cubic centimeters.
So then, given two of the variables, we can solve for density:


Therefore, the density of the bread is 0.6g per cubic centimeter.