In 1923, Bronsted and Lowry introduced a significant advancement in the understanding of acids and bases, refining earlier definitions established by Arrhenius. According to the Bronsted-Lowry theory, an acid is defined as a proton donor, specifically referring to the hydrogen ion (H+). This aligns with the Arrhenius definition, which states that an Arrhenius acid increases the concentration of H+ ions in aqueous solutions.
However, the Bronsted-Lowry theory diverges from Arrhenius in its definition of bases. While Arrhenius defined a base as a substance that produces hydroxide ions (OH-) in water, Bronsted and Lowry proposed that a base is a proton acceptor. This means that a base can accept H+ ions, which is often facilitated by the presence of lone pairs of electrons or a negative charge. This fundamental shift allows for the consideration of acid-base reactions in non-aqueous solutions, broadening the scope of acid-base chemistry.
Both theories agree on the behavior of acids: Bronsted-Lowry acids donate H+ ions, which is consistent with the Arrhenius definition. However, the Bronsted-Lowry approach emphasizes the interaction between acids and bases, highlighting that they always exist in pairs known as conjugate acid-base pairs. These pairs differ by a single hydrogen ion. For example, in the pair consisting of H2O and OH-, water (H2O) can donate an H+ to become OH-, while H3O+ (hydronium ion) and H2O also form a conjugate pair, differing by one H+ ion.
Understanding these concepts is crucial for grasping the dynamics of acid-base reactions and their applications in various chemical contexts.