Methyl amine in not an acid, but a (weak) base, pKb=3.36. It is comparable with the even weaker ammonia, NH3, pKb=4.76:
CH3NH2 + H2O <<--> CH3NH3+ + OH-
The ionic equation for the reaction between hydrochloric acid (HCl) and methylamine (CH3NH2) is: HCl + CH3NH2 -> CH3NH3+ + Cl-
The reaction is:CH3NH2 + HBr = CH3NH3Br
NH3 is a weak base, but H2CO3 ( carbonic acid ) is not a strong acid. It is a weak acid.
Since the conjugate acid is supposed to be just the addition of an H+, then it should be either HPH3+ or PH4+, phosphonium cations, resulting from protonation of phosphine. It has a molar mass of 35.01 g/molThe (positive) cations are much like the analogue ammonium ions NH4+.
The Kb value for CH3NH2(aq) is 4.4 x 10^-4.
The ionic equation for the reaction between hydrochloric acid (HCl) and methylamine (CH3NH2) is: HCl + CH3NH2 -> CH3NH3+ + Cl-
The reaction is:CH3NH2 + HBr = CH3NH3Br
NH3 is a weak base, but H2CO3 ( carbonic acid ) is not a strong acid. It is a weak acid.
Since the conjugate acid is supposed to be just the addition of an H+, then it should be either HPH3+ or PH4+, phosphonium cations, resulting from protonation of phosphine. It has a molar mass of 35.01 g/molThe (positive) cations are much like the analogue ammonium ions NH4+.
Among these NH3 is the weakest base so strongest conjugate acid would be NH4+ ion.
CH3NH2 + HCl ------> CH3NH3+Cl-
CH3NH2 is methyl amine, and it is ORGANIC.
no
The Kb value for CH3NH2(aq) is 4.4 x 10^-4.
Kb = [CH3NH3 +] [OH-] / [CH3NH2]
Isomers have equal chemical formula while having different chemical structures. CH3NH2 does not have different chemical structures with the same chemical formula. Therefor CH3NH2 is not an isomer.
Yes, CH3NH2 can have a resonance structure. The lone pair on the nitrogen can delocalize to form a double bond with the carbon, resulting in resonance stabilization.