Answer:
As it gets hydrolyzed easily.
Explanation:
The isocyanic acid may get polymerizes easily into cyanuric acid and a polymer cyamelide
Also, even at 0 °C temperature it may react with mositure and gets hydrolyzed into ammonia an carbon dioxide. Thus we generally prepare it in situ. Even after synthesis it is stroed at dry ice or liquid nitrogen at very low temperature.
The lewis structure is shown in the figure.
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.
