Answer:
b mi disputa se eu não asetar
Answer:
The four resonance structures of the phenoxide ion are shown in the image attached
The conjugate base of cyclohexanol has only one resonance contributor, while
the conjugate base of phenol has four resonance contributors.
Explanation:
In organic chemistry, it is known that structures are more stable if they possess more resonance contributors. The greater the number of contributing canonical structures, the more stable the organic specie. Since the phenoxide ion has four contributing canonical structures, it is quite much more stable than cyclohexanol having only one contributing structure to its conjugate base. Hence the PKa(acid dissociation constant) of phenol is lesser than that of cyclohexanol. The conjugate base of phenol is stabilized by resonance.
Answer:
In the reaction between p-aminophenol and acetic anhydride to form acetaminophen, 4.5 ml of water were added. This was done to recover the product out the container. Water was used as a means of carrying out the product out the container. However, it should be noted that we would want a small amount to be added in order to avoid the product dissolving onto it.
Explanation:
The rate at which the substance dissolves in water.
Answer: Synthesis
Explanation: I think is suynthesis