The correct option is A 5.4
(CH3)3NH+ (aq)+H2O (l)⇌(CH3)3N (aq)+H3O+ (aq)Initially: c 0 0Change: −cα cα cαEquilibrium:c−cα cα cα
We know , aqueous solution at room temperature has,
Ka×Kb=KwHere, Kw=10−14→Ionisation Constant for H2OKa=KwKbKa=10−146.4×10−5=1.56×10−10
By definition, the dissociation constant will be :
Ka=[(CH3)3N]×[H3O+][(CH3)3NH+]=cα×cαc−cα
Ka=0.1α×0.1α0.1−0.1α
Since dissociation of weak base is less so, 0.1−0.1α≈0.1
∴Ka=(0.1)2α20.1=1.56×10−10Ka=(0.1)α2=1.56×10−10α2=1.56×10−9
α=√1.56×10−9=3.95×10−5
[H3O+]=cα=0.1×3.95×10−5=3.95×10−6
pH=−log[H3O+]⇒pH=−log(3.95×10−6)=6−log3.95≈6−log4=6−0.6=5.4