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:
Boiling - when the liquid is heated to a gas.
Evaporating - when the air temperature is hotter than the surface of the liquid so the water turns into water vapor or a gas.
Explanation:
It's classified as an acid
Transition metals usually
Answer:
Explanation:
(a) melting point of S,S-hydrobenzoin should be 140°C. Since S,S-hydrobezoin and R,R-hydrobenzoin are enantiomeric pair so that their melting point and boilong point should be same.
(b) different melting point,
Racemic mixture must have different melting point in comparison to the pure enantiomers.
considering a racemic mixture, individual enantiometer possesses a greater affinity for its kind of molecules than for those of the other enantiometer
