Why This Matters
Inorganic chemistry exams don't just ask you to identify compounds—they test whether you understand why compounds behave the way they do. When you see H2SO4 on a question, you're being tested on acid-base theory, oxidation states, and industrial applications all at once. The compounds in this guide represent the foundational categories you'll encounter repeatedly: acids and bases, ionic salts, molecular compounds, and oxidizing agents. Master these, and you'll have the building blocks for predicting reactivity, writing balanced equations, and explaining real-world chemistry.
Don't just memorize formulas and names—know what concept each compound illustrates. Can you explain why NaOH is a strong base while NH3 is weak? Why KMnO4 oxidizes other species? These are the connections that separate students who struggle from those who ace the exam. Each compound below is grouped by its chemical behavior, so you're learning patterns, not just facts.
Strong Acids: Complete Dissociation and Industrial Workhorses
Strong acids dissociate completely in aqueous solution, releasing all their H+ ions. This complete ionization is what makes them powerful proton donors and essential reagents in industrial processes.
Hydrochloric Acid (HCl)
- Monoprotic strong acid—dissociates completely into H+ and Cl− ions in water
- Biological role in gastric juice where it maintains stomach pH around 1.5–3.5 for protein digestion
- Neutralization reactions with bases produce salt and water, a classic exam equation type
Sulfuric Acid (H2SO4)
- Diprotic acid and dehydrating agent—can donate two protons and removes water from compounds
- Industrial significance makes it the most-produced chemical globally, essential for fertilizers and batteries
- Highly corrosive due to both its acidity and its ability to generate heat when mixed with water
Nitric Acid (HNO3)
- Strong acid and strong oxidizing agent—the nitrogen in HNO3 has a +5 oxidation state, making it electron-hungry
- Industrial applications include fertilizer production (ammonium nitrate) and explosives manufacturing
- Passivation reactions with metals like aluminum form protective oxide layers, a testable concept
Compare: HCl vs. HNO3—both are strong monoprotic acids, but HNO3 is also an oxidizing agent while HCl is not. If an exam asks about acids that can dissolve noble metals like gold, HNO3 (in aqua regia) is your answer.
Strong Bases: Hydroxide Ion Donors
Strong bases dissociate completely to release OH− ions. Their reactivity stems from the hydroxide ion's ability to accept protons and attack electrophilic centers.
Sodium Hydroxide (NaOH)
- Complete dissociation in water releases Na+ and OH− ions, making it a strong Arrhenius base
- Saponification reactions with fats produce soap, a classic application in organic-inorganic crossover questions
- Industrial scale uses include paper manufacturing, textile processing, and drain cleaners
Compare: NaOH vs. NH3—both are bases, but NaOH dissociates completely while NH3 only partially accepts protons (Kb=1.8×10−5). This distinction between strong and weak bases is heavily tested.
Weak Bases and Amphoteric Compounds
Weak bases only partially accept protons in solution, establishing equilibrium. Understanding equilibrium position is key to predicting buffer behavior and pH calculations.
Ammonia (NH3)
- Weak base behavior—accepts a proton to form NH4+, but the equilibrium lies far to the left
- Nitrogen cycle importance as a key intermediate in converting atmospheric N2 to biologically usable forms
- Fertilizer production via the Haber process (N2+3H2→2NH3) is an industrial chemistry staple
Sodium Bicarbonate (NaHCO3)
- Amphoteric character—can act as either acid or base depending on the reaction partner
- Decomposition reaction with acids produces CO2 gas, the basis for baking leavening
- Buffer component in the bicarbonate buffer system, critical for blood pH regulation
Compare: NH3 vs. NaHCO3—both are weak bases, but NaHCO3 is amphoteric and can also donate a proton. FRQs love asking about species that can act as both acids and bases.
Ionic Salts: Electrolytes and Biological Function
Ionic compounds dissolve in water to form electrolyte solutions. The ions released determine conductivity, osmotic pressure, and biological signaling.
Sodium Chloride (NaCl)
- 1:1 electrolyte—dissociates into Na+ and Cl−, creating a neutral solution (neither ion hydrolyzes significantly)
- Osmotic balance in cells depends on NaCl concentration gradients across membranes
- Lattice energy of 787 kJ/mol explains its high melting point and solubility behavior
Potassium Chloride (KCl)
- Essential electrolyte—K+ ions are critical for nerve impulse transmission and muscle contraction
- Fertilizer component provides potassium, one of the three primary plant macronutrients (N-P-K)
- Medical applications include IV fluids and treatment for hypokalemia
Calcium Carbonate (CaCO3)
- Acid-base reaction with HCl produces CO2: CaCO3+2HCl→CaCl2+H2O+CO2
- Geological significance as the primary component of limestone, marble, and marine shells
- Thermal decomposition at high temperatures yields CaO (quickite) and CO2, a key industrial process
Compare: NaCl vs. KCl—structurally identical ionic compounds with different cations. The larger K+ ion means lower lattice energy for KCl and different biological roles. Expect questions on ion size effects.
Molecular Compounds: Covalent Bonding and Unique Properties
These compounds feature covalent bonds and exhibit properties tied to molecular structure. Intermolecular forces—not ionic interactions—determine their physical behavior.
Water (H2O)
- Hydrogen bonding network creates anomalously high boiling point, surface tension, and specific heat
- Universal solvent properties arise from its polarity and ability to stabilize ions through hydration
- Amphoteric behavior—can act as acid (donating H+) or base (accepting H+) depending on reaction partner
Carbon Dioxide (CO2)
- Linear, nonpolar molecule—despite polar C=O bonds, the symmetric geometry cancels dipole moments
- Acid anhydride behavior—dissolves in water to form carbonic acid: CO2+H2O⇌H2CO3
- Greenhouse gas that absorbs infrared radiation due to asymmetric stretching vibrations
Hydrogen Peroxide (H2O2)
- Oxygen oxidation state of -1—intermediate between O2 (0) and H2O (-2), making it both oxidizer and reducer
- Disproportionation reaction: 2H2O2→2H2O+O2, catalyzed by MnO2 or catalase
- Bleaching mechanism involves oxidation of chromophores, destroying color-causing structures
Compare: H2O vs. H2O2—both contain hydrogen and oxygen, but the extra oxygen in H2O2 creates an unstable O-O bond. This instability makes H2O2 a powerful oxidizer while H2O is remarkably stable.
These compounds readily accept electrons from other species. High oxidation states on central atoms drive their oxidizing power.
Potassium Permanganate (KMnO4)
- Mn in +7 oxidation state—the highest possible for manganese, making it a powerful electron acceptor
- Color change indicator—purple MnO4− reduces to colorless Mn2+ (acidic) or brown MnO2 (neutral/basic)
- Titration standard for redox reactions, especially with oxalic acid and iron(II) compounds
Iron(III) Chloride (FeCl3)
- Lewis acid behavior—the Fe3+ ion accepts electron pairs, catalyzing Friedel-Crafts reactions
- Hydrolysis in water produces acidic solutions due to Fe3+ coordinating water and releasing H+
- Coagulant in water treatment—neutralizes colloidal particles, allowing them to aggregate and settle
Copper Sulfate (CuSO4)
- Hydration behavior—anhydrous form is white; addition of water produces blue CuSO4⋅5H2O (blue vitriol)
- Water detection test—color change from white to blue confirms presence of water in unknown samples
- Agricultural fungicide due to Cu2+ toxicity to fungal cells
Compare: KMnO4 vs. FeCl3—both are oxidizing agents, but KMnO4 is much stronger (Mn goes from +7 to +2) while FeCl3 is milder (Fe stays at +3 but acts as Lewis acid). Choose KMnO4 for vigorous oxidations, FeCl3 for catalysis.
Quick Reference Table
|
| Strong acids (complete dissociation) | HCl, H2SO4, HNO3 |
| Strong bases | NaOH |
| Weak bases | NH3, NaHCO3 |
| Amphoteric species | H2O, NaHCO3 |
| Oxidizing agents | KMnO4, HNO3, H2O2 |
| Ionic electrolytes | NaCl, KCl, CaCO3 |
| Hydrogen bonding compounds | H2O, NH3, H2O2 |
| Transition metal compounds | CuSO4, FeCl3, KMnO4 |
Self-Check Questions
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Which two compounds from this guide can act as both an acid and a base (amphoteric behavior), and what structural feature enables this?
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Compare HCl and HNO3: both are strong acids, but only one is also a strong oxidizing agent. Which one, and why does its molecular structure enable oxidation?
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If you needed to identify the presence of water in an unknown sample, which compound would you use and what observable change would confirm a positive result?
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Rank NaOH, NH3, and NaHCO3 from strongest to weakest base. What determines the strength difference between them?
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An FRQ asks you to explain why KMnO4 is purple in solution but becomes colorless or brown after reacting with a reducing agent. What's happening to the manganese, and how does oxidation state relate to color?