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:
evaporation?
Explanation:
evaporate the water leaving behind the sand?
Answer is: Kb for methylamine is 4.37·10⁻⁴.<span>
Chemical reaction: CH</span>₃NH₂ + H₂O → CH₃NH₃⁺ + OH⁻.
c(CH₃NH₂) = 0.253 M.
α = 4.07% ÷ 100% = 0.0407.
[CH₃NH₃⁺] = [OH⁻] = c(CH₃NH₂) · α.
[CH₃NH₃⁺] = [OH⁻] = 0.253 M · 0.0407.
[CH₃NH₃⁺] = [OH⁻] = 0.0103 M.
[CH₃NH₂] = 0.253 M - 0.0103 M.
[CH₃NH₂] = 0.2427 M.
Kb = [CH₃NH₃⁺] · [OH⁻] / [CH₃NH₂].
Kb = (0.0103 M)² / 0.2427 M.
Kb = 4.37·10⁻⁴.
Answer:742 torr= approximately 0.976 atm
Explanation:
Since we know that one atm= 760 torr, we can compute the following calculation:
(742 torr/1)*(1atm/760torr)=0.976316 atm
Remember sig figs (3) to round it to 0.976 atm
*
=0.976316=0.976 atm
(torr cancels out and we're left with atm)
Hope this helps :)