Acids and Bases Chapter 2 PDF

WILLIAM H. BROWN THOMAS POON www.wiley.com/college/brown CHAPTER TWO Acids and Bases Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-1 Arrhenius Acids and Bases In 1884, Svante Arrhenius proposed these definitions: – Acid: A substance that dissolves in water to...

WILLIAM H. BROWN THOMAS POON www.wiley.com/college/brown CHAPTER TWO Acids and Bases Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-1 Arrhenius Acids and Bases In 1884, Svante Arrhenius proposed these definitions: – Acid: A substance that dissolves in water to produce hydronium ions (H3O+). – Base: A substance that dissolves in water to produce hydroxide ions (OH–). – This definition of an acid is a slight modification of the original Arrhenius definition, which was that an acid produces H+ in aqueous solution. – Today we know that H+ reacts immediately with a Copyright water© 2017 molecule to Inc. John Wiley & Sons, give a reserved. All rights hydronium2-2 ion Arrhenius Acids and Bases When HCl, for example, dissolves in water, it reacts with water to give a hydronium ion and a chloride ion. Insert equation top page 41 We use curved arrows to show the change in position of electron pairs during this reaction. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-3 Arrhenius Acids and Bases With bases, the situation is slightly different. – Many bases are metal hydroxides such as KOH, NaOH, Mg(OH)2, and Ca(OH)2. – These compounds are ionic solids and, when they dissolve in water, their ions merely separate. – Bases that are not metal hydroxides produce OH– by reacting with water molecules. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-4 Arrhenius Acids and Bases – We use curved arrows to show the transfer of a proton from water to ammonia. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-5 Brønsted-Lowry Acids & Bases Acid: A proton donor. Base: A proton acceptor. Conjugate base: The species formed from an acid when an acid donates a proton to a base. Conjugate acid: The species formed from a base when the base accepts a proton from an acid. – Acid-base reaction: A proton-transfer reaction. – Conjugate acid-base pair: Any pair of molecules or ions that can be interconverted by transfer of a proton. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-6 Conjugate Acids & Bases We illustrate these relationships by the reaction of hydrogen chloride with water: Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-7 Brønsted-Lowry Acids & Bases Brønsted-Lowry definitions do not require water as a reactant. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-8 Brønsted-Lowry Acids & Bases We use curved arrows to show the flow of electrons that occurs in the transfer of a proton from acetic acid to ammonia. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-9 Brønsted-Lowry Acids & Bases Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-10 Brønsted-Lowry Acids & Bases Note the following about the conjugate acid-base pairs in Table 2.1: 1. An acid can be positively charged, neutral, or negatively charged; examples of each type are H3O+, H2CO3, and H2PO4–. 2. A base can be negatively charged or neutral; examples are OH–, Cl–, and NH3. 3. Acids are classified a monoprotic, diprotic, or triprotic depending on the number of protons that each may give up; examples are HCl, H2CO3, and H3PO4. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-11 Brønsted-Lowry Acids & Bases Carbonic acid, for example, can give up one proton to become bicarbonate ion, and then the second proton to become carbonate ion. 4. Several molecules and ions appear in both the acid and conjugate base columns; that is, each can function as both an acid and as a base. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-12 Brønsted-Lowry Acids & Bases 5. There is an inverse relationship between the strength of an acid and the strength of its conjugate base. – The stronger the acid, the weaker its conjugate base. – HI, for example, is the strongest acid in Table 2.1 and its conjugate base, I–, is the weakest base in the table. – CH3COOH (acetic acid) is a stronger acid that H2CO3 (carbonic acid); conversely, CH3COO– (acetate ion) is a weaker base that HCO3– (bicarbonate ion). Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-13 Acid and Base Strength Strong acid: One that reacts completely or almost completely with water to form H3O+ ions. Strong base: One that reacts completely or almost completely with water to form OH– ions. – Here are the six most common strong acids and the four most common strong bases. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-14 Acid and Base Strength Weak acid: A substance that only partially dissociates in water to produce H3O+ ions. – Acetic acid, for example, is a weak acid; in water, only 4 out every 1000 molecules are converted to acetate ions. Weak base: A substance that only partially dissociates in water to produce OH– ions. – ammonia, for example, is a weak base. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-15 Acid-Base Reactions Acetic acid is incompletely ionized in aqueous solution. The equation for the ionization of a weak acid, HA, is: Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-16 pKa Values for Some Organic and Inorganic Acids Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-17 Acid-Base Equilibria To determine the position of equilibrium in an acid- base reaction: – Identify the two acids in the equilibrium; one on the left and one on the right. – Use the information in Table 2.2 to determine which is the stronger acid and which is the weaker acid. – Remember that the stronger acid gives the weaker conjugate base, and the weaker acid gives the stronger conjugate base. – The stronger acid reacts with the stronger base to give the weaker acid and weaker base. – Equilibrium lies on the side of the weaker acid and the weaker base. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-18 Acid-Base Equilibrium Equilibrium in the following acid-base reaction lies to the right, on the side of the weaker acid and the weaker base. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-19 Structure and Acidity The most important factor in determining the relative acidity of an organic acid is the relative stability of the anion, A–, formed when the acid, HA, transfers a proton to a base. We consider these four factors: 1. The electronegativity of the atom bonded to H in HA. 2. Resonance stabilization of A–. 3. The inductive effect. 4. The size and delocalization of charge Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. in A –. 2-20 Structure and Acidity Electronegativity of the atom bearing the negative charge. Within a period – The greater the electronegativity of the atom bearing the negative charge, the more strongly its electrons are held. – The more strongly electrons are held, the more stable the anion A–. – The more stable the anion A–, the greater the acidity of the acid HA. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-21 Structure and Acidity Resonance delocalization of the charge on A– – Compare the acidity of a carboxylic acid and an alcohol, both of which contain an –OH group. – Carboxylic acids are weak acids. Values of pKa for most unsubstituted carboxylic acids fall within the range of 4 to 5. – Alcohols are very weak acids. Values of pKa for most alcohols fall within the range of 15 to 18. – How do we account for the fact that carboxylic acids are stronger acids than alcohols? Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-22 Structure and Acidity – The greater the resonance stabilization of the anion, the more acidic the compound. – There is no resonance stabilization in an alkoxide anion. – We can write two equivalent contributing structures for the carboxylate anion; the negative charge is delocalized evenly over the two oxygen atoms. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-23 Structure and Acidity Inductive polarization of electron density transmitted through covalent bonds caused by a nearby atom of higher electronegativity Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-24 Structure and Acidity The more stable the anion A–, the greater the acidity of the acid HA. – The larger the volume over which the charge on an anion (or cation) is delocalized, the greater the stability of the anion (or cation). – When considering the relative acidities of the hydrogen halides, (HI > HBr > HCl > HF), we need to consider the relative stabilities of the halide ions. – Recall from general chemistry that atomic size is a periodic property. – For main group elements, atomic radii increase going down a group and increase going across a period. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-25 Structure and Acidity – For the halogens, iodine has the largest atomic radii, fluorine has the smallest I > Br > Cl > F. – Anions are always larger than the atoms from which they are derived. For anions, nuclear charge is unchanged but the added electron(s) introduce new repulsions and the electron cloud swells. – Among the halide ions, I– has the largest atomic radius, and F– has the smallest atomic radius. – Thus, HI is the strongest acid because the negative charge on iodide ion is delocalized over a larger volume than the negative charge on chloride, etc. – The result of both resonance and the inductive effect is due to the delocalization of charge. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-26 Lewis Acids and Bases Lewis acid: Any molecule or ion that can form a new covalent bond by accepting a pair of electrons. Lewis Base: Any molecule or ion that can form a new covalent bond by donating a pair of electrons. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-27 Lewis Acids and Bases – When HCl dissolves in water, for example, the strongest available Lewis base is an H2O molecule, and the following proton-transfer reaction takes place. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-28 Lewis Acids and Bases – When HCl dissolves in methanol, the strongest available Lewis base is a CH3OH molecule, and the following proton-transfer reaction takes place. Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-29 Lewis Acids and Bases Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-30 Lewis Acids and Bases Another type of Lewis acid we will encounter in later chapters is an organic cation in which a carbon is bonded to only three atoms and bears a positive formal charge. – such carbon cations are called carbocations Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-31 Acids and Bases End Chapter 2 Copyright © 2017 John Wiley & Sons, Inc. All rights reserved. 2-32