Acids, Bases and Salt Preparations (2d)

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Last updated 3:29 PM on 3/14/26
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25 Terms

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Solubility: Sodium, Potassium and Ammonium Salts

All soluble

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Solubility: Nitrates

All soluble

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Solubility: Chlorides

most, except Silver and Lead(II)

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Solubility: Sulfates

most, except Barium, Calcium and Lead(II)

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Solubility: Carbonates

most insoluble, except Sodium, Potassium and Ammonium

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Solubility: Hydroxides

most insoluble, except Sodium, Potassium and Ammonium

(Calcium Hydroxide is slightly soluble)

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Proton Transfer: Acids

proton donors

  • ionize in solutions → produce protons, H+ ions

  • H+ ions make aqueous solution acidic

  • ex: HCl

HCl (aq)   →    H+ (aq)    +    Cl (aq)

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Proton Transfer: Bases

proton acceptors

  • ionize in solutions → produce OH- ions that accept protons

  • OH- ions make aqueous solution alkaline

  • ex: NaOH

NaOH (s)   →    Na+ (aq)    +    OH (aq)

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Metal + Acid Reactions

  • only metals above hydrogen react with dilute acids

  • more reactive metal = more vigorous reaction

  • K and Na: dangerous, explosive reaction

  • reaction forms salt and hydrogen gas

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Metal + Acid general equation

metal + acid → salt + hydrogen gas

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Acid + Base Reactions

  • produces salt and water

  • identity of salt depends on acid used and base’s positive ions

2HCl + CuO ⟶ CuCl2 + H2O

H2SO4 + 2NaOH ⟶ Na2SO4 + 2H2O

HNO3 + KOH ⟶ KNO3 + H2O

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Acids + Metal Carbonates

  • forms metal salt, carbon dioxide and water

  • distinguishable because of effervescence caused by carbon dioxide gas

2HCl + Na2CO3 ⟶ 2NaCl + H2O + CO2

H2SO4 + CaCO3⟶ CaSO4 + H2O + CO2

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Bases vs Alkali

  • water soluble base = alkali

  • alkaline pH: >7

  • turn red litmus paper blue

  • bases: usually oxides, hydroxides or carbonates of metals

  • OH- ions makes aqueous solutions alkaline

  • ammonia is an exceptional base because it produces OH- ions

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Soluble Salt Preparation

  • reaction of acid and insoluble base

  • insoluble reactant added in excess to ensure all the acid has reacted

  • if not, unreacted acid becomes dangerously concentrated during evaporation and crystallisation

  • excess reactant is filtered to ensure only salt and water remain

  • since all acid has reacted, excess solid base removed → solution left can only be salt and water

  • water evaporated until small crystals appear

    • usually when half the water is left

    • evaporating slowly over many days = larger crystals

  • if carbonate used, CO2 released into atmosphere

  • ex: preparing copper(II) sulfate from copper(II) oxide and dilute sulfuric acid

CuO (s) + H2SO(aq) ⟶ CuSO(aq) + H2O (l)

<ul><li><p>reaction of acid and insoluble base</p></li><li><p>insoluble reactant added in excess to ensure all the acid has reacted</p></li><li><p>if not, unreacted acid becomes dangerously concentrated during evaporation and crystallisation</p></li><li><p>excess reactant is filtered to ensure only salt and water remain</p></li><li><p>since all acid has reacted, excess solid base removed → solution left can only be salt and water</p></li><li><p>water evaporated until small crystals appear</p><ul><li><p>usually when half the water is left</p></li><li><p>evaporating slowly over many days = larger crystals</p></li></ul></li><li><p>if carbonate used, CO<sub>2 </sub>released into atmosphere</p></li><li><p>ex: preparing copper(II) sulfate from copper(II) oxide and dilute sulfuric acid</p></li></ul><p><strong>                  CuO (s) + H<sub>2</sub>SO<sub>4&nbsp;</sub>(aq)&nbsp;⟶&nbsp;CuSO<sub>4&nbsp;</sub>(aq) + H<sub>2</sub>O (l)</strong></p>
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Soluble Salt Preparation with a Metal

acid can also be reacted with a metal to produce a salt, where:

  • metal is above hydrogen in the reactivity series

  • no too reactive that a dangerous reaction takes place

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Soluble Salt Preparation using Titration

  • use pipette to measure alkali into conical flask

  • add drops of indicator (phenolphthalein or methyl orange)

  • add acid into burette, note starting volume

  • add acid very slowly from burette until indicator changes to correct colour

  • note and record final volume, calculate volume of acid added (starting - final acid volume)

  • add this volume of acid into same volume of alkali without indicator

  • heat to partially evaporate, leaving saturated solution

  • leave to crystallise decant excess solution, allow crystals to dry

<ul><li><p>use pipette to measure alkali into conical flask</p></li><li><p>add drops of indicator (phenolphthalein or methyl orange)</p></li><li><p>add acid into burette, note starting volume</p></li><li><p>add acid very slowly from burette  until indicator changes to correct colour</p></li><li><p>note and record final volume, calculate volume of acid added (starting - final acid volume)</p></li><li><p>add this volume of acid into same volume of alkali without indicator</p></li><li><p>heat to partially evaporate, leaving saturated solution</p></li><li><p>leave to crystallise decant excess solution, allow crystals to dry</p></li></ul><p></p>
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Insoluble Salt Preparation

  • precipitation reaction

  • solid salt is precipitate → solid salt formed must be insoluble

  • pattern:

    • soluble salt 1 + soluble salt 2 ⟶  insoluble salt + soluble salt 3

    • AB + CD ⟶ AD + CB

  • measure out fixed volume of one solution and add second salt solution until in slight excess → ensures max. amount of precipitate obtained

  • precipitate recovered by filtration, washed with distilled water to remove residue (recovering solid) contaminating reactants → left to dry

  • good way to prepare silver and lead(II) salts which are often insoluble → starting material = usually nitrates of silver or lead(II) since all nitrates are soluble

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Practical (Preparing Copper(II) Sulfate): Aim

to prepare a pure, dry sample of hydrated copper(II) sulfate crystals

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Practical (Preparing Copper(II) Sulfate): Materials

  • 1.0 mol / dm3 dilute sulfuric acid

  • copper(II) oxide

  • spatula & glass rod

  • measuring cylinder & 100 cm3 beaker

  • Bunsen burner

  • tripod, gauze & heatproof mat

  • filter funnel & paper, conical flask

  • evaporating basin and dish.

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Practical (Preparing Copper(II) Sulfate): Diagram

<p></p>
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Practical (Preparing Copper(II) Sulfate): Method

  • add 50 cc dilute acid into beaker

  • warm gently with a Bunsen burner

  • add copper(II) oxide slowly into hot dilute acid

  • stir until base is in excess (stops dissolving, suspension forms in acid)

  • filter mixture into evaporating basin → remove excess bases

  • gently het solution in water bath or with electric heater → evaporate water and saturate solution

  • check solution saturation by dipping cold glass rod and seeing if crystals form on the end

  • leave filtrate in a warm place to dry and crystallise

  • decant excess solution and allow to dry

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Practical (Preparing Copper(II) Sulfate): Excess Base Added

  • added in excess to use up all the acid

    • acid would become dangerously concentrated during evaporation and crystallisation

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Practical (Preparing Copper(II) Sulfate): Results

hydrated copper(II) sulfate crystals should be bright blue, regularly shaped

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Practical (Preparing Lead(II) Sulfate): Aim

  • prepare a dry sample of lead(II) sulfate

  • solid salt obtained = precipitate → solid salt formed must be insoluble, reactants must be soluble

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Practical (Preparing Lead(II) Sulfate): Method

  • add 25 cc of 0.5 mol dm3 lead(II) nitrate solution to a small beaker

  • add 25 cc of 0.5 mol dm3 potassium nitrate to the beaker and mix with stirring rod

  • filter to remove precipitate from mixture

  • wash filtrate with distilled water to remove traces of other solutions

  • leave in oven to dry

Soluble salt 1 = lead(II) nitrate       

Soluble salt 2 = potassium sulfate

lead(II) nitrate + potassium sulfate → lead(II) sulfate + potassium nitrate

Pb(NO3)2  (aq) + K2SO4 (aq) → PbSO4 (s) + 2KNO3 (aq)