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
Because Methyl amine has a bigger Kb value (4.4 x 10^-4) than ammonia (1.8 x 10^-5). The Kb value is the base dissociation constant, so with a bigger base dissociation constant, Methyl amine is more basic --> forms more OH- in solution.
- AP Chemistry student
methyleamine is a stronger Lewis base
No. dimethylamine is a weak base.
weak
Ammonia is a weak basic (alkaline) with a pH of 11.5. Ammonia is weak because it only partially ionizes.
No. Ammonia is a base. The ammonium ion is weakly acidic.
F is the stronger base because it is bigger than Cl
Ammonia is a base so it turns red litmus paper blue.
I believe it turns blue. Ammonia is a base, so whatever color red litmus paper turns when it's in contact with a base!
How am I suppose to know huh
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-
Sodium Hydroxide is a stronger base than Ammonia
piperidine
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.
The conjugate base of methane (CH4) is the methyl carbanion (CH3-). Because methane is an extremely weak acid, the methyl carbanion is an EXTREMELY STRONG BASE. Compounds like methyl lithium (CH3Li) are, in fact, considered organometallic superbases and will violently deprotonate even the weakest acids (such as water and ammonia).
There is no real basis for comparison but nitric acid is a strong acid and ammonia is a weak base.
It is under the definition of a Lewis base. Amines are usually considered weak bases, but methylamine is highly nucleophilic. It is a derivative of ammonia with a methyl group replacing a hydrogen atom. Ammonia is also highly basic.
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.
"Methylamine is a good nucleophile as it is highly basic and unhindered, although, as an amine it is considered a weak base. Its use in organic chemistry is pervasive. Some reactions involving simple reagents include: with phosgene to methyl isocyanate, with carbon disulfide and sodium hydroxide to the sodium methyldithiocarbamate, with chloroform and base to methyl isocyanide and with ethylene oxide tomethylethanolamines."
Saturated Hydrocarbons are neither acids nor bases