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On the other hand, if a chemical is a weak acid its conjugate base will not necessarily be strong. Consider that ethanoate, the conjugate base of ethanoic acid, has a base splitting constant (Kb) of about 5.6 × 10 −10, making it a weak base. In order for a species to have a strong conjugate base it has to be a very weak acid, like water.
Azanide is the IUPAC-sanctioned name for the anion NH − 2. The term is obscure; derivatives of NH − 2 are almost invariably referred to as amides, [1] [2] [3] despite the fact that amide also refers to the organic functional group – C(=O)−NR 2. The anion NH − 2 is the conjugate base of ammonia, so it is formed by the self-ionization ...
A Lewis base is often a Brønsted–Lowry base as it can donate a pair of electrons to H +; [11] the proton is a Lewis acid as it can accept a pair of electrons. The conjugate base of a Brønsted–Lowry acid is also a Lewis base as loss of H + from the acid leaves those electrons which were used for the A—H bond as a lone pair on the ...
A conjugate base is formed when the acid is deprotonated by the base. In the image above, hydroxide acts as a base to deprotonate the carboxylic acid. The conjugate base is the carboxylate salt. In this case, hydroxide is a strong enough base to deprotonate the carboxylic acid because the conjugate base is more stable than the base because the ...
A simple buffer solution consists of a solution of an acid and a salt of the conjugate base of the acid. For example, the acid may be acetic acid and the salt may be sodium acetate . The Henderson–Hasselbalch equation relates the pH of a solution containing a mixture of the two components to the acid dissociation constant , K a of the acid ...
2 Na + 2 NH 3 → 2 NaNH 2 + H 2. NaNH 2 is a salt-like material and as such, crystallizes as an infinite polymer. [5] The geometry about sodium is tetrahedral. [6] In ammonia, NaNH 2 forms conductive solutions, consistent with the presence of [Na(NH 3) 6] + and NH − 2 ions.
The conjugate base of phthalimide is potassium phthalimide. These anion can be alkylated to give N-alkylimides, which in turn can be degraded to release the primary amine. Strong nucleophiles, such as potassium hydroxide or hydrazine are used in the release step. Treatment of imides with halogens and base gives the N-halo derivatives
Lithium amide or lithium azanide is an inorganic compound with the chemical formula LiNH 2. It is a white solid with a tetragonal crystal structure. [1] Lithium amide can be made by treating lithium metal with liquid ammonia: [2] 2 Li + 2 NH 3 → 2 LiNH 2 + H 2. Lithium amide decomposes into ammonia and lithium imide upon heating. [3]