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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.
H 2 O is a base because it accepts a proton from CH 3 COOH and becomes its conjugate acid, the hydronium ion, (H 3 O +). [9] The reverse of an acid–base reaction is also an acid–base reaction, between the conjugate acid of the base in the first reaction and the conjugate base of the acid.
Deprotonation (or dehydronation) is the removal (transfer) of a proton (or hydron, or hydrogen cation), (H +) from a Brønsted–Lowry acid in an acid–base reaction. [1] [2] The species formed is the conjugate base of that acid. The complementary process, when a proton is added (transferred) to a Brønsted–Lowry base, is protonation (or ...
In chemistry, protonation (or hydronation) is the adding of a proton (or hydron, or hydrogen cation), usually denoted by H +, to an atom, molecule, or ion, forming a conjugate acid. [1] (The complementary process, when a proton is removed from a Brønsted–Lowry acid, is deprotonation.) Some examples include The protonation of water by ...
A weak acid or the conjugate acid of a weak base can be treated using the same formalism. Acid HA: HA ⇌ H + + A −; Base A: HA + ⇌ H + + A; First, an acid dissociation constant is defined as follows. Electrical charges are omitted from subsequent equations for the sake of generality
In chemistry, a Lewis conjugate may refer to: The conjugate acid of a Lewis base or the conjugate base of a Lewis acid A molecule having a conjugated system of bonds in its Lewis structure
where [H +] is the equilibrium concentration of H +, K a is the acid dissociation constant, C a and C b are the analytical concentrations of the acid and its conjugate base, respectively, and Δ = [H +] − [OH −]. The equation can be solved for [H +] by using the autoionization constant for water, K w, to introduce [OH −] = K w /[H +].
Formate salts have the formula M(O 2 CH)(H 2 O) x. Such salts are prone to decarboxylation. For example, hydrated nickel formate decarboxylates at about 200 °C with reduction of the Ni 2+ to finely powdered nickel metal: Ni(HCO 2) 2 (H 2 O) 2 → Ni + 2 CO 2 + 2 H 2 O + H 2. Such fine powders are useful as hydrogenation catalysts. [1]