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A conjugate acid, within the Brønsted–Lowry acid–base theory, is a chemical compound formed when an acid gives a proton (H +) to a base—in other words, it is a base with a hydrogen ion added to it, as it loses a hydrogen ion in the reverse reaction.
Upon treatment with an acid, sulfide salts convert to hydrogen sulfide: S 2− + H + → SH − SH − + H + → H 2 S. Oxidation of sulfide is a complicated process. Depending on the conditions, the oxidation can produce elemental sulfur, polysulfides, polythionates, sulfite, or sulfate. Metal sulfides react with halogens, forming sulfur and ...
Its conjugate acid is hydrogen sulfide (H 2 S). However, bisulfide's basicity stems from its behavior as an Arrhenius base. A solution containing spectator-only counter ions, has a basic pH according to the following acid-base reaction:
The acid, HA, is a proton donor which can lose a proton to become its conjugate base, A −. The base, B, is a proton acceptor which can become its conjugate acid, HB +. Most acid–base reactions are fast, so the substances in the reaction are usually in dynamic equilibrium with each other. [8]
Disulfite is the conjugate base of disulfurous acid (pyrosulfurous acid), which originates from sulfurous acid in accordance with the dehydration reaction above: 2 H 2 SO 3 → 2 HSO − 3 + 2 H + → H 2 S 2 O 5 + H 2 O. The disulfite ion also arises from the addition of sulfur dioxide to the sulfite ion:
If it is the result of a reaction between a strong acid and a strong base, the result is a neutral salt. Weak acids reacted with weak bases can produce ionic compounds with both the conjugate base ion and conjugate acid ion, such as ammonium acetate. Some ions are classed as amphoteric, being able to react with either an acid or a base. [59]
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A variety of amines and nitrogen heterocycles are useful bases of moderate strength (pK a of conjugate acid around 10-13) . N,N-Diisopropylethylamine (DIPEA, also called Hünig's Base [1]), pK a = 10.75