acids, bases and salts

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61 Terms

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acid → definition

an acid is a substance that can donate a proton (H^+) to another substance

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base → definition

a base is a substance that can accept a proton (H^+) from another substance

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examples of acids

  1. hydrochloric acid (HCl) → H+ and Cl-

  2. sulfuric acid (H_2SO_4) → H+ and SO_4^{2-}

  3. nitric acid (HNO_3) → H+ and NO_3^-

  4. phosphoric acid (H_3PO_4) → H+ and PO_4^{3-}

  5. carbonic acid (H_2CO_3) → H+ and CO_3^{2-}

  6. ethanoic acid (CH_3CO_2H) → H+ and CH_3CO_2^-

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examples of alkalis

  1. sodium hydroxide (NaOH) → OH- and Na+

  2. potassium hydroxide (KOH) → OH- and K^+

  3. calcium hydroxide (Ca(OH)_2) → OH- and Ca^{2+}

  4. aqueous ammonia (NH_3) → OH- and NH_4+

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aqueous ammonia as a base

NH_3 (aq) + H_2O (l) ⇌ NH_4+ (aq) + OH- (aq)

  • aqueous ammonia can dissolve in water and take in protons

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strong acid → definition

a strong acid is one which dissociates fully in solution to give protons(H^+)

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strong acid

  • degree of dissociation: approximately 100%

  • type of arrow used in dissociation equation: → (single arrow)

  • monobasic: HNO_3

  • dibasic: H_2SO_4

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monobasic → definition

one mole of H^+ is dissociated per mole of an acid

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dibasic → definition

2 moles of H^+ is dissociated per mole of an acid

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strong base → definition

a strong base is one which dissociates fully in solution to give hydroxide ions (OH^-)

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strong base

  • degree of dissociation: approximately 100%

  • type of arrow used in dissociation equation: → (single arrow)

  • monobasic: KOH

  • dibasic: Ca(OH)_2

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weak acid → definition

a weak acid is one which dissociates partially in solution to give protons (H^+)

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weak acid

  • degree of dissociation: <<< 100%

  • type of arrow used in dissociation equation: ⇌ (half arrow)

  • examples: organic acids

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weak base → definition

a weak base is one which dissociates partially in solution to give hydroxide ions (OH^-)

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weak base

  • degree of dissociation: <<< 100%

  • type of arrow used in dissociation equation: ⇌ (half arrow)

  • examples: ammonia

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strength → definition

strength of an acid is a measure of the extent/percentage of dissociation of an acid in solution

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concentration → definition

concentration of an acid is the number of moles of undissociated acid per unit volume

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power of hydrogen (pH) → definition

the pH of a solution is defined as the negative logarithm to the base 10 of the concentration of hydrogen ions [H^+] in solution in mol dm^{-3}

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formula for pH

  • pH = -log_{10}[H^+]

  • [H^+] = 10 ^{-pH}

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pH value and concentration of hydrogen ions [H^+]

  • the larger the pH value, the smaller the [$H^+$]

    • acidic: more H^+ than OH^- → lower pH

    • alkali: more OH^- than H^+ → higher pH

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pH scale

at 25°C:

  • neutral solution: [H^+] = [OH^-] → pH = 7

  • acidic solution: [H^+] > [OH^-] → pH < 7 (1-6)

  • alkaline solution: [H^+] < [OH^-] → pH > 7 (8-14)

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indicators → definition

indicators are dyes or a mixture of dyes which change colour when added to acids or alkalis

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physical properties of acids

  • have a sour taste

  • have pH less than 7

  • turn damp blue litmus paper red

  • may be solids (e.g. citric acid), liquids (e.g. concentrated sulfuric acid) or gases (e.g. hydrogen chloride gas)

  • can conduct electricity

    • can act as charge carriers as they exist as free mobile ions in aqueous solutions

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physical properties of alkalis

  • have a bitter taste and feel soapy

  • have pH greater than 7

  • turn damp red litmus paper blue, turn universal indicator blue or violet

  • can conduct electricity

    • can act as charge carriers as they exist as free mobile ions in aqueous solution

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neutralisation → definition

neutralisation refers to the reaction between an acid and a base to form salt and water

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common operating conditions for Haber process

  1. high pressure of 250 atm → force the reaction in a certain direction

  2. moderate temperature of 450°C → reaction itself produces a lot of heat

  3. iron catalyst

  4. molar ratio of N_2 : H_2 is 1 : 3

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acid-base nature of period 3 oxide

trend: the nature of the oxides change from basic (metal oxides) to amphoteric to acidic (non-metal oxides) across the periods

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group 1 and group 2 → metal oxides

  • elements: Na (group 1) and Mg (group 2)

  • formula: Na_2O and MgO → giant ionic lattice (structure)

  • acid-base nature: basic

    • dissolves to form alkalis

    • behaves as bases which can react with acids

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group 13 → metal oxide

  • elements: Al

  • formula: Al_2O_3 → giant ionic lattice (structure)

  • acid-base nature: amphoteric

    • properties of both acids and base → reacts with both acids and bases

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group 14, group 15 and group 16 → non-metal oxide

  • elements: Si (group 14), P (group 15) and S (group 16)

  • formula: SiO_2; P_4O_6, P_4O_10; SO_2, SO_3 → covalent

    • P_4O_6: phosphorus (III) oxide

    • P_4O_{10}: phosphorus (V) oxide

  • acid-base nature: acidic

    • dissolves in water to form an acid

    • behaves as acids which can react with bases

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basic oxides

  • can react with acids to form salt and water

  • usually insoluble in water (some can dissolve to form alkalis)

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basic oxides and reaction with water

  1. Na_2O + H_2O → 2NaOH

  2. K_2O + H_2O → 2KOH

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basic oxides and reaction with acids

  1. Na_2O + 2HCl → 2NaCl + H_2O

  2. K_2O + 2HCl → 2KCl + H_2O

  3. MgO + 2HCl → MgCl_2 + H_2O

  4. CaO + 2HCl → CaCl_2 + H_2O

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acidic oxides

  • can react with bases to form salt and water

  • some can dissolve in water to form acidic solutions

    • SiO_2 not soluble in water due to its giant molecular structure and numerous strong covalent bonds

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acidic oxides and reaction with water

  • SO_2 + H_2O → H_2SO_3 (sulfurous acid)

  • SO_3 + H_2O → H_2SO_4(sulfuric acid)

  • P_4O_6 + 6H_2O → 4H_3PO_3 (phosphorous acid)

  • P_4O_{10} + 6H_2O → 4H_3PO_4 (phosphoric acid)

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acidic oxides and reaction with bases

  • P_4O_{10} (s) + 12NaOH (aq) → 4Na_3PO_4 (aq) + 6H_2O (l)

  • P_4O_6 + 8NaOH → 4Na_2HPO_3 + 2H_2O

  • SO_2 (g) + 2NaOH (aq)→ Na_2SO_3 (aq) + H_2O (l)

  • SO_3 (g) + 2NaOH (aq) → Na_2SO_4 (aq) + H_2O (l)

  • SiO_2 (s) + 2NaOH (l) - 350°C → Na_2SiO_3 (l) + H_2O (g)

<ul><li><p><span>P_4O_{10} (s) + 12NaOH (aq) → 4Na_3PO_4 (aq) + 6H_2O (l)</span></p></li><li><p><span>P_4O_6 + 8NaOH → 4Na_2HPO_3 + 2H_2O</span></p></li><li><p><span>SO_2 (g) + 2NaOH (aq)→ Na_2SO_3 (aq) + H_2O (l)</span></p></li><li><p><span>SO_3 (g) + 2NaOH (aq) → Na_2SO_4 (aq) + H_2O (l)</span></p></li><li><p><span>SiO_2 (s) + 2NaOH (l) - 350°C → Na_2SiO_3 (l) + H_2O (g)</span></p></li></ul>
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amphoteric oxides

  • react with acids and bases to form salt and water

  • do not react with water

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amphoteric examples

  1. aluminium oxide (Al_2O_3)

  2. lead (II) oxide (PbO)

  3. zinc oxide (ZnO)

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amphoteric oxides and reaction with acid

Al_2O_3 + 6HCl → 2AlCl_3 + 3H_2O

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amphoteric oxides and reaction with base

Al_2O_3 + 2NaOH + 3H_2O → 2NaAl(OH)_4

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neutral oxides

  • will not react with acids/bases → no reaction at all

  • examples: carbon monoxide (CO), water ($H_2O$), nitric oxide (NO) and nitrous oxide ($N_2O$)

  • reaction with acids and bases:

    • neutral oxides do not react with acids or bases

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salts

  • ionic compounds

  • to determine type of reagents that could be used to form a salt → analyse the cations and anions of the salt

  • water of crystallisation in many hydrated salts can be driven off by heating the crystals of the salt strongly to form anhydrous salts

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water of crystallisation

water bonded chemically within the crystals

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hydrated salts

salts that contain water of crystallisation

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anhydrous salts

salts that do not contain water of crystallisation

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to name hydrated salts

  • the left hand side denotes the salt

  • the dot (.) denotes the presence of water of crystallisation

  • the right hand side denotes the water of crystallisation

<ul><li><p>the left hand side denotes the salt</p></li><li><p>the dot (.) denotes the presence of water of crystallisation</p></li><li><p>the right hand side denotes the water of crystallisation</p></li></ul>
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formation of salts

  1. acid + metal → salt + hydrogen gas

  2. acid + carbonate → salt + water + carbon dioxide gas

  3. acid + base → salt + water (neutralisation)

  4. ammonium salt + base → salt + water + ammonia gas

    • need heat to dry off ammonia gas

  5. 2 soluble (aqueous) reagent → insoluble salt

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reactivity series

  • K (most reactive) → Na → Ca → Mg → Al → Zn → Fe → Pb → H (H^+ acid) → Cu → Ag → Au (least reactive)

    • K and Na: highly reactive → explosive

    • K, Na, Ca, Mg, Al, Zn, Fe, Pb: more reactive than H → reacts with acids

    • Cu, Ag, Au: less reactive than H → will not react with acids

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reaction of an acid and a metal

  • when a reactive metal (above hydrogen in reactivity series) reacts with a dilute acid, salt and hydrogen gas are formed

  • metal + acid → salt + hydrogen gas

  • extremely reactive metals in the reactivity series (group 1 metals: sodium and potassium) react violently and explosively

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reaction of an acid and a carbonate/hydrogen carbonate

  • when a carbonate/hydrogen carbonate reacts with an acid, salt, water and carbon dioxide gas are formed

  • carbonate ({CO_3}^{2-}) + acid → salt + water + carbon dioxide gas

  • hydrogen carbonate ({HCO_3}^-) + acid → salt + water + carbon dioxide

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reaction of an acid and a base

  • when an acid reacts with a base, salt and water are formed

    • acid + base → salt + water

  • when ammonia reacts with an a acid, only a salt is formed

    • acid + ammonia (NH_3) → salt (cation: {NH_4}^+)

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reaction of an alkali and an ammonium salt

  • when an ammonium salt is warmed in the presence of an alkali, salt, water and ammonia gas are formed

    • ammonium salt ({NH_4}^+) + base - warm → salt + water + ammonia gas (NH_3)

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precipitation reactions

  • insoluble salts can be formed by a precipitation reaction through the mixing of two soluble (aqueous) reagents

  • when an aqueous solution that contains the anion of an insoluble salt is mixed with an aqueous solution that contains the cation of that salt → the insoluble salt will precipitate out of the mixture

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preparation of salt → guidelines

  • soluble salt: usually prepared from reactions with acids

  • insoluble salt: usually prepared by the precipitation method (mixing of two soluble salts)

<ul><li><p><span>soluble salt: usually prepared from reactions with acids</span></p></li><li><p><span>insoluble salt: usually prepared by the precipitation method (mixing of two soluble salts)</span></p></li></ul>
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reaction with acids

  • if salt to be prepared is soluble in water while reactants are soluble:

    1. reaction of acid with excess metal

    2. reaction of acid with excess base (insoluble in water)

    3. reaction of acid with excess carbonate (insoluble in water)

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reaction of an acid and excess metal

  • to produce a salt that is soluble in water, excess metal is used such that the acid is completely used up → limiting reagent

  • hydrogen gas will escape to the surroundings → only the soluble salt and the excess metal will remain in the reaction container at the end of the reaction

    • the soluble salt and excess metal can be easily separated through filtration

  • this method is not suitable for:

    • very reactive metals such as sodium and potassium → react violently with acids

    • metals below hydrogen in the reactivity series such as copper, silver and gold → do not react with dilute acids

<ul><li><p>to produce a salt that is soluble in water, excess metal is used such that the acid is completely used up → limiting reagent</p></li><li><p>hydrogen gas will escape to the surroundings → only the soluble salt and the excess metal will remain in the reaction container at the end of the reaction</p><ul><li><p>the soluble salt and excess metal can be easily separated through filtration</p></li></ul></li><li><p>this method is not suitable for:</p><ul><li><p>very reactive metals such as sodium and potassium → react violently with acids</p></li><li><p>metals below hydrogen in the reactivity series such as copper, silver and gold → do not react with dilute acids</p></li></ul></li></ul>
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reaction of an acid and excess insoluble base

  • a salt can be prepared by a reaction between a base (metal oxide or metal hydroxide) and an acid

  • the procedure for preparation of salt from recall of insoluble base and acid is similar to the procedure to prepare salt from acid and excess metal

<ul><li><p><span>a salt can be prepared by a reaction between a base (metal oxide or metal hydroxide) and an acid </span></p></li></ul><ul><li><p><span>the procedure for preparation of salt from recall of insoluble base and acid is similar to the procedure to prepare salt from acid and excess metal</span></p></li></ul>
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reaction of an acid with excess insoluble carbonate

  • carbonates and hydrogen carbonates can be soluble/insoluble in water

  • insoluble carbonate or hydrogen carbonate can be added in excess to an acid to produce a salt

<ul><li><p><span>carbonates and hydrogen carbonates can be soluble/insoluble in water</span></p></li><li><p><span>insoluble carbonate or hydrogen carbonate can be added in excess to an acid to produce a salt</span></p></li></ul>
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reaction of an acid with a soluble base or carbonate

  • to overcome problem, an experiment has to be carried out to determine the exact volume of alkali (soluble base) that reacts with a know amount of acid, in the presence of an indicator → titration

    • the reaction is complete when the indicator changes colour. the volumes of acids and alkalis used are noted

  • to prepare the salt, the experiment is repeated with the same amount of acid and alkali used, in absence of indicator → can cause contamination to the salt prepared

<ul><li><p><span>to overcome problem, an experiment has to be carried out to determine the exact volume of alkali (soluble base) that reacts with a know amount of acid, in the presence of an indicator → titration</span></p><ul><li><p><span>the reaction is complete when the indicator changes colour. the volumes of acids and alkalis used are noted</span></p></li></ul></li><li><p><span>to prepare the salt, the experiment is repeated with the same amount of acid and alkali used, in absence of indicator → can cause contamination to the salt prepared</span></p></li></ul><p></p>
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preparation of insoluble salts via ionic precipitation reaction

  • criteria

    1. choose 2 suitable ionic compounds that when combined will result in a precipitate of the desired solution

    2. necessary to dissolve any solid starting material to get an aqueous solution first

<ul><li><p><span>criteria</span></p><ol><li><p><span>choose 2 suitable ionic compounds that when combined will result in a precipitate of the desired solution</span></p></li><li><p><span>necessary to dissolve any solid starting material to get an aqueous solution first</span></p></li></ol></li></ul>
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sample question: why PbO(s) cannot be added directly to HI (aq) to prepare PbI_2 (s)

  • PbO + 2HI → PbI_2 + H_2O

  • reaction of PbO with HI forms insoluble PbI_2, which coats the surface of PbO solid. this protective layer prevents PbO from reacting with HI, leading to low yield of PbI_2