The pKa of CH3NH2, also known as methylamine, is approximately 10.7. This means that at a pH lower than 10.7, methylamine will predominantly exist in its protonated form, while at a pH higher than 10.7, it will exist primarily in its deprotonated form.
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 ionic equation for the reaction between hydrochloric acid (HCl) and methylamine (CH3NH2) is: HCl + CH3NH2 -> CH3NH3+ + Cl-
The Kb value for CH3NH2(aq) is 4.4 x 10^-4.
The pKa of diisopropylamine is around 10-11.
The pKa of bromoacetic acid is approximately 2.64.
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+.
CH3NH2 is methyl amine, and it is ORGANIC.
Since tha pka of the aniline ion is equal to 4.6, the anilinium ion is a stronger acid than the methylaminium ion, and aniline (c6h5nh2) is a weaker base than methylamine (ch3nh2).
The ionic equation for the reaction between hydrochloric acid (HCl) and methylamine (CH3NH2) is: HCl + CH3NH2 -> CH3NH3+ + Cl-
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The Kb value for CH3NH2(aq) is 4.4 x 10^-4.
The pKa of diisopropylamine is around 10-11.
Kb = [CH3NH3 +] [OH-] / [CH3NH2]
The pKa of bromoacetic acid is approximately 2.64.
The reaction is:CH3NH2 + HBr = CH3NH3Br
The pKa value of Doxofylline is approximately 4.22.
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.