How am I suppose to know huh
Because methyl is an electron pumping group and It pumps electrons to Amine group to make it basic, But Ammonia has no influence from any basic groups. Therefore compared to Methyl-Amine, Ammonia is less basic
A buffer solution of methyl amine (a weak base) and its conjugate acid, methyl amine ion (methylammonium ion), maintains a stable pH by resisting changes when small amounts of acid or base are added. When an acid is introduced, the methyl amine can neutralize it by accepting protons (H⁺), forming more methylammonium ions. Conversely, if a base is added, the methylammonium ions can donate protons to restore equilibrium. This equilibrium between the weak base and its conjugate acid allows the solution to effectively stabilize pH changes.
Dimethylamine is a stronger base than methylamine because it has two methyl groups attached to the nitrogen atom, which increases the electron-donating ability of the amine group. This leads to better stabilization of the resulting conjugate acid, making dimethylamine more basic than methylamine.
Piperidine is a stronger base compared to diethyl amine. This is due to the greater electron-releasing effect of the piperidine nitrogen lone pair, which makes it more available for donation in basic reactions.
Methyl amine is more basic than trimethyl amine because it is more stable. Basicity is based on the stability of a compound as well as the availability of the hydrogens present. With three methyl groups are far more unstable than one methyl group on a nitrogen, since all of the protons are pushing away from one another.
in the case of aniline, the lone pair on nitrogen is involved in resonance with the benzene ring, hence its basicity decreases. no such resonance is seen in cyclohexyl amine, and the lone pair is available to abstract protons and it is stronger base than aniline.
Methyl orange turns yellow when dipped in a base.
Methyl indicator is typically found in its protonated form, which means it has the potential to act as a weak base when it accepts a proton.
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-
Methyl orange is an acid-base indicator that changes color in the presence of acids and bases. In basic conditions, such as with a strong base like sodium hydroxide, methyl orange will turn yellow or orange.
Salts in amine solutions are formed through the reaction of amines with acids. When an amine, which is a basic compound, reacts with an acid, it accepts a proton (H+) from the acid, resulting in the formation of an ammonium ion. This ammonium ion then combines with the anion from the acid, leading to the formation of an amine salt. The process is an example of acid-base neutralization, where the amine acts as a base.
yellow