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
Ethanoic acid is a stronger acid in liquid ammonia because ammonia is a weaker base compared to water. Therefore, in liquid ammonia, ethanoic acid easily donates a proton to the ammonia molecules, forming the acetate ion. This proton transfer reaction is more favorable than in water due to the difference in the basicity of the solvent.
Ammonia is a weak basic (alkaline) with a pH of 11.5. Ammonia is weak because it only partially ionizes.
Hydrazine is more basic than ammonia because it has two amino groups compared to just one in ammonia. This allows hydrazine to donate more protons, enhancing its basicity. Additionally, the lone pair of electrons on each nitrogen in hydrazine is more readily available for accepting protons, making it a stronger base than ammonia.
F is the stronger base because it is bigger than Cl
acids wont change their color in methyl orange. bases changes the color when they are present in methyl orange.HCl is white or no color in methyl orange.Added:Red > orangy-yellow
How am I suppose to know huh
Neither is an acid. Both are bases, hydroxide is the stronger base.
Yes. Ammonia has a pKb of 4.75. Water has a pKb of 13.995.
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.
Sodium hydroxide is a stronger base compared to ammonia. This is because sodium hydroxide has a higher dissociation constant (pKa) and is more effective at donating hydroxide ions in solution, resulting in a higher pH compared to ammonia.
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 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 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.
There is no real basis for comparison but nitric acid is a strong acid and ammonia is a weak base.
Sodium hydroxide is stronger than ammonia because it is a strong base, dissociating completely in water to release hydroxide ions. On the other hand, ammonia is a weak base and only partially dissociates in water. This results in sodium hydroxide having a higher concentration of hydroxide ions, making it more reactive and stronger than ammonia.
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.
Ammonia is a stronger base than aniline because the lone pair on the nitrogen in ammonia is more readily available for donation compared to the nitrogen in aniline, which is partially delocalized due to resonance. As a result, ammonia is able to more effectively accept a proton to form its conjugate acid, making it a stronger base.