Q.Boric acid, , is described as a weak monobasic acid, yet it does not release a proton like a typical Brønsted acid. Explain how behaves as a Lewis acid in water, and write the equilibrium that produces the acidic solution.
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Start your 14-day free trial to unlock the full solution →Boron in orthoboric acid, , is hybridised and three-coordinate, surrounded by only six bonding electrons (three bonds to the three groups) and no lone pair; this leaves an empty orbital on boron, making the whole molecule electron-deficient and an effective Lewis acid — an electron-pair acceptor. When is dissolved in water, it does not ionise as a normal Brønsted acid would (by donating one of its own protons); instead, the electron-deficient boron atom accepts a lone pair of electrons from an incoming water molecule's oxygen, effectively capturing a hydroxide ion from that water molecule and releasing a proton from it. The overall equilibrium is:\n\nIn the product, boron is now four-coordinate, hybridised, in the tetrahydroxyborate ion , its octet now complete. Because a proton () does appear in solution as a net result, the solution measurably behaves as a weak acid, but the mechanism is fundamentally different from a classical Brønsted acid: boric acid works by accepting a hydroxide ion (indirectly generating from the water …
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