Acids, Bases & Salts – Comprehensive Bullet-Point Notes

Syllabus Focus (Valid for Examinations in & after March 2026)

• Study of acids, bases & salts with emphasis on:
– Ions present in mineral acids, alkalis & salts and in their aqueous solutions.
– Simple molecular definitions, characteristic properties, litmus & pH tests.
– Ionisation/dissociation equations for acids, bases & salts.
– Introduction and use of pH scale / Universal indicator.
– Classification & definition of normal, acid, basic salts.
– Decomposition of carbonates, bicarbonates, sulphites & sulphides by dilute acids (lab work mandatory).
– Six preparative routes for normal salts: direct combination, displacement, precipitation, neutralisation of an insoluble base, neutralisation of an alkali (titration), action of dilute acids on (bi)carbonates.

Key Definitions (Molecular View)

• Acid – compound that yields only hydronium ions in water. Example dissociation: HCl+2H<em>2O    H</em>3O++Cl\text{HCl} + 2\,\text{H}<em>2\text{O} \;\longrightarrow\; \text{H}</em>3\text{O}^+ + \text{Cl}^-
• Base – oxide or hydroxide of a metal (or NH<em>3\text{NH}<em>3 derivative) that reacts with hydronium ions to give salt + water only. E.g. CuO+2HClCuCl</em>2+H<em>2O\text{CuO} + 2\,\text{HCl} \rightarrow \text{CuCl}</em>2 + \text{H}<em>2\text{O} • Alkali – water-soluble base that furnishes only hydroxyl ions. Example: NaOH</em>(aq)Na++OH\text{NaOH}</em>{(aq)} \rightarrow \text{Na}^+ + \text{OH}^- (All alkalis are bases; converse is not true.)
• Salt – product of partial/complete replacement of ionisable H+\text{H}^+ of an acid by a metal or NH4+\text{NH}_4^+. Dissociates to give cation ≠ H+\text{H}^+ & anion ≠ OH\text{OH}^-.

Indicator Basics

• Indicators = weak organic acids/bases whose ionic/molecular forms have different colours → colour governed by [H+][\text{H}^+].
• Litmus: purple (neutral) → red (acidic) / blue (alkaline).
• Methyl orange: pink (pH < 3.1) → orange (3.1–4.4) → yellow (>4.4).
• Phenolphthalein: colourless (pH < 8.3) → pink (8.3–10.0).
• Universal indicator / pH paper: continuous colour graduation, pH 0 (red) → 7 (green) → 14 (violet).

pH Concept

• Ionic product of water: K<em>w=[H+][OH]=1014  mol2dm6  (25C)K<em>w = [\text{H}^+][\text{OH}^-] = 10^{-14}\;\text{mol}^2\,\text{dm}^{-6}\;(25^{\circ}\text{C}). • pH=log</em>10[H+]\text{pH} = -\log</em>{10}[\text{H}^+] (mol dm$^{-3}$).
• Pure water: [H+]=107[\text{H}^+] = 10^{-7} → pH 7 (neutral).
• pH < 7 acidic, pH > 7 basic; farther from 7 → stronger.

Classification of Acids

  1. By source
    – Organic (plant-derived): citric, oxalic, tartaric, acetic (weak).
    – Inorganic (mineral): HCl,  H<em>2SO</em>4,  HNO3\text{HCl},\;\text{H}<em>2\text{SO}</em>4,\;\text{HNO}_3 (generally strong).

  2. By composition
    – Hydracids: only H + non-metal (no O) e.g. HCl,  HI\text{HCl},\;\text{HI}.
    – Oxyacids: H + element + O e.g. HNO<em>3,  H</em>2SO4\text{HNO}<em>3,\;\text{H}</em>2\text{SO}_4.

  3. By strength (degree of ionisation)
    – Strong: nearly 100 % dissociation → solution contains almost only ions. Examples HCl,  H<em>2SO</em>4,  HNO3\text{HCl},\;\text{H}<em>2\text{SO}</em>4,\;\text{HNO}_3.
    – Weak: partial dissociation, equilibrium mixture of molecules & ions (acetic, citric, carbonic, formic).

  4. By concentration
    – Concentrated: high proportion of acid (>1 mol dm$^{-3}$).
    – Dilute: <1 mol dm$^{-3}$.

  5. By basicity (no. of ionisable hydrogens)
    – Monobasic: HCl,  HNO<em>3,  CH</em>3COOH\text{HCl},\;\text{HNO}<em>3,\;\text{CH}</em>3\text{COOH}.
    – Dibasic: H<em>2SO</em>4,  H<em>2CO</em>3\text{H}<em>2\text{SO}</em>4,\;\text{H}<em>2\text{CO}</em>3 (two-step ionisation).
    – Tribasic: H<em>3PO</em>4\text{H}<em>3\text{PO}</em>4 (three-step, gives 3 salt types).

Classification of Bases / Alkalis

• By acidity (replaceable OH\text{OH}^- per formula unit)
– Monoacidic: NaOH,  KOH,  NH<em>4OH\text{NaOH},\;\text{KOH},\;\text{NH}<em>4\text{OH}. – Diacidic: Ca(OH)</em>2,  Cu(OH)<em>2\text{Ca(OH)}</em>2,\;\text{Cu(OH)}<em>2 (sparingly soluble). – Triacidic: Al(OH)</em>3,  Fe(OH)<em>3\text{Al(OH)}</em>3,\;\text{Fe(OH)}<em>3 (insoluble). • Strength parallels acid logic: strong alkalis (LiOH, NaOH, KOH) vs weak (NH$4$OH, Ca(OH)$_2$). Concentration terminology as for acids.

Hydronium & Hydroxyl Ion Formation (Particle Pictures)

• Hydronium: H+\text{H}^+ from acid binds lone pair on O of H<em>2O\text{H}<em>2\text{O} forming H</em>3O+\text{H}</em>3\text{O}^+ via coordinate covalent bond OH\text{O}\rightarrow\text{H}.
HClwaterH++Cl;H++H<em>2OH</em>3O+\text{HCl} \xrightarrow[]{\text{water}} \text{H}^+ + \text{Cl}^-;\quad \text{H}^+ + \text{H}<em>2\text{O} \rightarrow \text{H}</em>3\text{O}^+
• Hydroxyl: H<em>2O\text{H}<em>2\text{O} donates H+\text{H}^+ to electron-rich NH</em>3\text{NH}</em>3NH4++OH\text{NH}_4^+ + \text{OH}^-, bond NH\text{N}\rightarrow\text{H}.

Preparation of Acids (Representative)

  1. Direct union of non-metal with H$2$ (at elevated T/light): H</em>2+Cl22HCl\text{H}</em>2 + \text{Cl}_2 \rightarrow 2\,\text{HCl}.

  2. Dissolving acidic oxides in water: CO<em>2+H</em>2OH<em>2CO</em>3\text{CO}<em>2 + \text{H}</em>2\text{O} \rightarrow \text{H}<em>2\text{CO}</em>3; SO<em>3+H</em>2OH<em>2SO</em>4\text{SO}<em>3 + \text{H}</em>2\text{O} \rightarrow \text{H}<em>2\text{SO}</em>4.

  3. From salts via displacement with conc. H<em>2SO</em>4\text{H}<em>2\text{SO}</em>4 (<200C200^{\circ}\text{C}): NaCl+H<em>2SO</em>4NaHSO4+HCl\text{NaCl} + \text{H}<em>2\text{SO}</em>4 \rightarrow \text{NaHSO}_4 + \text{HCl}\uparrow.

  4. Oxidation of non-metals: S+6HNO<em>3H</em>2SO<em>4+2H</em>2O+6NO2\text{S} + 6\,\text{HNO}<em>3 \rightarrow \text{H}</em>2\text{SO}<em>4 + 2\,\text{H}</em>2\text{O} + 6\,\text{NO}_2.

Preparation of Bases (Representative)

• Metal + O$2$ → basic oxide; soluble oxide + H$2$O → alkali. Example 2K+2H<em>2O2KOH+H</em>22\text{K} + 2\text{H}<em>2\text{O} \rightarrow 2\text{KOH} + \text{H}</em>2.
• Thermal decomposition of carbonates/nitrates: 2Pb(NO<em>3)</em>2Δ2PbO+4NO<em>2+O</em>22\text{Pb(NO}<em>3)</em>2 \xrightarrow{\Delta} 2\text{PbO} + 4\,\text{NO}<em>2 + \text{O}</em>2.
• Precipitating hydroxides: AlCl<em>3+3NaOH3NaCl+Al(OH)</em>3\text{AlCl}<em>3 + 3\text{NaOH} \rightarrow 3\text{NaCl} + \text{Al(OH)}</em>3\downarrow.

Physical Properties Snapshot

Acids: sour, corrosive (strong mineral acids), turn blue litmus red.
Bases/alkalis: bitter, soapy, caustic (NaOH/KOH), turn red litmus blue.

Core Chemical Reactions

• Neutralisation (ionic): H+<em>(aq)+OH</em>(aq)H<em>2O</em>(l)\text{H}^+<em>{(aq)} + \text{OH}^-</em>{(aq)} \rightarrow \text{H}<em>2\text{O}</em>{(l)}; exothermic (heat of neutralisation per Eq. gram-equiv.).
• Metal + dilute acid (except HNO<em>3\text{HNO}<em>3 for Na/K/Ca) liberates H$2$: Zn+2HClZnCl<em>2+H</em>2\text{Zn} + 2\text{HCl} \rightarrow \text{ZnCl}<em>2 + \text{H}</em>2.
• Less-volatile acid displaces more-volatile acid from salt on heating: NaNO<em>3+H</em>2SO<em>4NaHSO</em>4+HNO<em>3\text{NaNO}<em>3 + \text{H}</em>2\text{SO}<em>4 \rightarrow \text{NaHSO}</em>4 + \text{HNO}<em>3\uparrow. • Alkali + ammonium salt → ammonia liberation: NH</em>4Cl+NaOHΔNaCl+NH<em>3+H</em>2O\text{NH}</em>4\text{Cl} + \text{NaOH} \xrightarrow{\Delta} \text{NaCl} + \text{NH}<em>3\uparrow + \text{H}</em>2\text{O}.

Uses (Selected)

Acids: boric acid (eye-wash), citric (preserves), oxalic (ink remover), carbonic (soft drinks), tartaric (baking powder), acetic (vinegar), HCl (pickling metals).
Bases: NaOH (soap), Ca(OH)$2$ (bleaching powder), Mg(OH)$2$ / Al(OH)$3$ (antacids), Ca(OH)$2$ (water softening, degreasing).

Acid Rain Reference

• pH < 5.6 precipitation containing H<em>2SO</em>4,  H<em>2SO</em>3,  HNO<em>3,  HNO</em>2\text{H}<em>2\text{SO}</em>4,\;\text{H}<em>2\text{SO}</em>3,\;\text{HNO}<em>3,\;\text{HNO}</em>2 formed from anthropogenic SO<em>2,  NO</em>x\text{SO}<em>2,\;\text{NO}</em>x.
• Reaction chain: SO<em>2+H</em>2OH<em>2SO</em>3\text{SO}<em>2 + \text{H}</em>2\text{O} \rightarrow \text{H}<em>2\text{SO}</em>3; 2SO<em>2+O</em>22SO32\text{SO}<em>2 + \text{O}</em>2 \rightarrow 2\text{SO}_3 etc.
• Effects: soil nutrient leaching, aquatic pH drop, infrastructural corrosion.

Salts – Detailed Classification

  1. Normal salts: complete H-replacement; no ionisable H. Eg Na<em>2SO</em>4\text{Na}<em>2\text{SO}</em>4.

  2. Acid salts: partial replacement, retain replaceable H; show acidic properties. Eg NaHSO<em>4,  NaHCO</em>3\text{NaHSO}<em>4,\;\text{NaHCO}</em>3.

  3. Basic salts: contain metallic cation + OH\text{OH}^- + acid anion (from incomplete neutralisation of polybasic base). Eg Cu(OH)Cl,  Cu(OH)NO3\text{Cu(OH)Cl},\;\text{Cu(OH)NO}_3.

  4. Double salts: crystalline combination of two simple salts that dissociate to give both ions in solution (e.g. potash alum K<em>2SO</em>4Al<em>2(SO</em>4)<em>324H</em>2O\text{K}<em>2\text{SO}</em>4\,\cdot\,\text{Al}<em>2(\text{SO}</em>4)<em>3\,\cdot\,24\text{H}</em>2\text{O}, Mohr’s salt (NH<em>4)</em>2SO<em>4FeSO</em>46H2O\text{(NH}<em>4)</em>2\text{SO}<em>4\,\cdot\,\text{FeSO}</em>4\,\cdot\,6\text{H}_2\text{O}).

  5. Mixed salts: two different positive or negative radicals inside one formula, e.g. NaKCO3,  Ca(OCl)Cl\text{NaKCO}_3,\;\text{Ca(OCl)Cl}.

  6. Complex salts: yield complex ion in solution; e.g. K<em>2[HgI</em>4],  Na[Ag(CN)<em>2],  Na</em>2ZnO<em>2,  [Cu(NH</em>3)<em>4]SO</em>4\text{K}<em>2[\text{HgI}</em>4],\;\text{Na[Ag(CN)}<em>2],\;\text{Na}</em>2\text{ZnO}<em>2,\;[\text{Cu(NH}</em>3)<em>4]\text{SO}</em>4.

Solubility Rules (Cold Water)

• Always soluble: Na+,  K+,  NH<em>4+\text{Na}^+,\;\text{K}^+,\;\text{NH}<em>4^+ salts; all nitrates/nitrites; all bicarbonates; most chlorides & sulphates. • Sparingly/insoluble exceptions: – PbSO</em>4,  AgSO<em>4,  CaSO</em>4,  BaSO<em>4\text{PbSO}</em>4,\;\text{AgSO}<em>4,\;\text{CaSO}</em>4,\;\text{BaSO}<em>4. – PbCl</em>2\text{PbCl}</em>2 (soluble in hot water), AgCl,  HgCl\text{AgCl},\;\text{HgCl}.
– All sulphites, sulphides, carbonates, oxides, hydroxides, phosphates (except Na/K/NH$_4$ derivatives).

General Synthetic Routes for Salts

  1. Direct combination (synthesis): 2Fe+3Cl<em>22FeCl</em>32\text{Fe} + 3\text{Cl}<em>2 \rightarrow 2\text{FeCl}</em>3.

  2. Displacement (active metal + dil. acid): Zn+H<em>2SO</em>4ZnSO<em>4+H</em>2\text{Zn} + \text{H}<em>2\text{SO}</em>4 \rightarrow \text{ZnSO}<em>4 + \text{H}</em>2.

  3. Precipitation (double decomposition): Pb(NO<em>3)</em>2+2NaCl2NaNO<em>3+PbCl</em>2\text{Pb(NO}<em>3)</em>2 + 2\text{NaCl} \rightarrow 2\text{NaNO}<em>3 + \text{PbCl}</em>2\downarrow.

  4. Neutralisation of insoluble base: CuO+H<em>2SO</em>4CuSO<em>4+H</em>2O\text{CuO} + \text{H}<em>2\text{SO}</em>4 \rightarrow \text{CuSO}<em>4 + \text{H}</em>2\text{O}.

  5. Neutralisation of an alkali (titration): 2NaOH+H<em>2SO</em>4Na<em>2SO</em>4+2H2O2\text{NaOH} + \text{H}<em>2\text{SO}</em>4 \rightarrow \text{Na}<em>2\text{SO}</em>4 + 2\text{H}_2\text{O}.

  6. Action of dilute acids on (bi)carbonates: Na<em>2CO</em>3+2HCl2NaCl+H<em>2O+CO</em>2\text{Na}<em>2\text{CO}</em>3 + 2\text{HCl} \rightarrow 2\text{NaCl} + \text{H}<em>2\text{O} + \text{CO}</em>2.

Step-wise Preparations (Laboratory Protocol Highlights)

• Iron(III) chloride (volatile, deliquescent): heat Fe wire in dry Cl$2$ stream; sublimate FeCl</em>3\text{FeCl}</em>3 vapours into chilled receiver; store with fused CaCl<em>2\text{CaCl}<em>2. • FeSO$4$·7H$2$O / ZnSO$4$·7H$2$O: treat Fe or Zn with dil. H</em>2SO<em>4\text{H}</em>2\text{SO}<em>4 → filter, concentrate, crystallise green (Fe) or colourless (Zn) heptahydrate. • PbCl$2$: convert insoluble PbO\text{PbO} or PbCO<em>3\text{PbCO}<em>3 to soluble Pb(NO</em>3)<em>2\text{Pb(NO}</em>3)<em>2 via dil. HNO</em>3\text{HNO}</em>3, then precipitate with NaCl\text{NaCl}; dissolve ppt in hot water & cool → needle crystals.
• CaCO$3$: mix aq. CaCl</em>2\text{CaCl}</em>2 + Na<em>2CO</em>3\text{Na}<em>2\text{CO}</em>3 → white ppt, wash & dry to amorphous powder.
• CuSO$4$·5H$2$O: react black CuO\text{CuO} (or blue Cu(OH)<em>2\text{Cu(OH)}<em>2) with warm dil. H</em>2SO<em>4\text{H}</em>2\text{SO}<em>4; filter, concentrate & crystallise blue pentahydrate. • Na$
2$SO$4$·10H$2$O (titration): standardise neutralisation of NaOH with dil. H<em>2SO</em>4\text{H}<em>2\text{SO}</em>4 using phenolphthalein → evaporate neutral solution & crystallise Glauber’s salt.

Hydrolysis Behaviour of Salts (Solution pH)

Salt type

Example

Products of hydrolysis

Nature of solution

Weak base + strong acid

NH4Cl\text{NH}_4\text{Cl}

NH4OH+HCl\text{NH}_4\text{OH} + \text{HCl}

Slightly acidic

Strong base + weak acid

NaHCO<em>3,  Na</em>2CO3\text{NaHCO}<em>3,\;\text{Na}</em>2\text{CO}_3

NaOH+H<em>2CO</em>3\text{NaOH} + \text{H}<em>2\text{CO}</em>3

Alkaline

Strong base + strong acid

NaCl\text{NaCl}

NaOH+HCl\text{NaOH} + \text{HCl} (no net change)

Neutral

Water of Crystallisation, Deliquescence & Efflorescence

• Water of crystallisation fixed (loose) combination: gypsum (CaSO<em>42H</em>2O\text{CaSO}<em>4\cdot2\text{H}</em>2\text{O}), blue vitriol (CuSO<em>45H</em>2O\text{CuSO}<em>4\cdot5\text{H}</em>2\text{O}), washing soda (Na<em>2CO</em>310H<em>2O\text{Na}<em>2\text{CO}</em>3\cdot10\text{H}<em>2\text{O}). • Deliquescent salts absorb moisture until they liquefy: FeCl</em>3,  CaCl<em>2\text{FeCl}</em>3,\;\text{CaCl}<em>2 (anh.), MgCl</em>2\text{MgCl}</em>2.
• Efflorescent salts lose water, crumble to powder: Na<em>2SO</em>410H<em>2O,  MgSO</em>47H2O\text{Na}<em>2\text{SO}</em>4\cdot10\text{H}<em>2\text{O},\;\text{MgSO}</em>4\cdot7\text{H}_2\text{O}.

Field / Industrial Significance of pH & Indicators

• Agriculture: match soil pH to crop (citrus: slightly alkaline, rice: acidic, sugarcane: neutral).
• Dairy: souring milk detected when pH drops below 6.6.
• Medicine: diagnostic pH testing of blood (≈7.4) & urine; antacid formulation.
• Technology: biochemical & organic syntheses carried out under controlled pH windows.

Representative pH Values (25 °C)

0.1N  HCl0.1\,\text{N}\;\text{HCl} ≈ pH 1.0; 0.1N  H<em>2SO</em>40.1\,\text{N}\;\text{H}<em>2\text{SO}</em>4 ≈ 1.2.
• Vinegar (acetic) ≈ 2.9; grape juice (tartaric) ≈ 3.5.
• Milk (lactic) ≈ 6.6; human blood ≈ 7.3.
• Sea water ≈ 8.5; 0.1N  NH4OH0.1\,\text{N}\;\text{NH}_4\text{OH} ≈ 11.1; 0.1N  NaOH0.1\,\text{N}\;\text{NaOH} ≈ 13.0.


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