Metals and Non-metals — Complete Grade 10 Chemistry Guide
Part 1: everything for your exam, with diagrams you can draw · Part 2: going further — India's metallurgical firsts, metallic bonding and recycling, fully referenced
An iron gate left outside for a couple of rainy seasons is already crumbling with rust.
Why the difference? And where does iron come from at all, when no one has ever dug a lump of pure iron out of a field? By the end of Part 1 you can answer both. Part 2 reveals what scientists at IIT Kanpur discovered inside the pillar itself.
| Topic | Metals and Non-metals |
| Age group | 14–16 years (Grade 9–10) |
| You need first | Electron arrangement, displacement reactions, acids |
| Diagrams to draw | Dot-and-cross (ionic), electrolytic refining, rusting test tubes |
| Reading time | Part 1 about 30 min · Part 2 about 12 min |
- Reactivity series: K > Na > Ca > Mg > Al > Zn > Fe > Pb > [H] > Cu > Hg > Ag > Au
- Metal + oxygen → basic oxide; Al2O3 and ZnO are amphoteric (react with acids and bases)
- Na and K are stored under kerosene (paraffin oil) — they catch fire in air
- Ionic bond = metal gives electrons, non-metal takes them (Na+Cl−)
- Ionic compounds: high melting point, soluble in water, conduct when molten or dissolved — never as a solid
- Extraction: top of series = electrolysis · middle = roast/calcine then reduce with carbon · bottom = heat alone
- Roasting = sulfide heated in excess air · calcination = carbonate heated in limited air
- Refining: impure metal = anode, thin pure strip = cathode
- Rusting needs both air and water
Which syllabus are you studying?
| Point | India — NCERT / CBSE | UK — GCSE / IGCSE | USA — NGSS / Honors |
|---|---|---|---|
| Order of metals | Reactivity series | Reactivity series (often with C and H placed in it) | Activity series |
| Drawing ionic bonds | Electron-dot structure | Dot-and-cross diagram | Lewis dot structure |
| Metallic bonding | not taught at Class 10 | taught — "sea of delocalised electrons" | taught |
| Extracting aluminium | electrolytic reduction of Al2O3 | electrolysis with cryolite (Higher tier) | less emphasis |
| Refining copper | electrolytic refining | electrolytic purification | rarely examined |
| Spelling | aluminium, sulphide | aluminium, sulfide | aluminum, sulfide |
1. Physical properties
| Property | Metals | Non-metals |
|---|---|---|
| Lustre | shiny | dull — except iodine |
| Hardness | usually hard — except Na, K (cut with a knife) | usually soft — except diamond, the hardest natural substance |
| Malleability | can be beaten into sheets — gold and silver most of all | brittle — shatter |
| Ductility | can be drawn into wire — 1 g of gold gives about 2 km of wire | no |
| Heat conduction | good — silver and copper best; lead and mercury poor | poor |
| Electrical conduction | good | poor — except graphite |
| Sonorous | ring when struck — which is why bells are metal | no |
| State at room temperature | solid — except mercury (liquid) | solid or gas — bromine is liquid |
| Melting point | usually high — except gallium, caesium (melt in your palm) | usually low |
2. Chemical properties of metals
(a) Metal + oxygen → metal oxide
4Al(s) + 3O2(g) → 2Al2O3(s)
Most metal oxides are basic. A few react with both acids and bases — these are amphoteric oxides:
Al2O3 + 2NaOH → 2NaAlO2 + H2O — with a base (sodium aluminate)
| Metal | With oxygen | With water | With dilute acid |
|---|---|---|---|
| K, Na | catch fire in air — stored under kerosene | violent with cold water; H2 ignites | dangerously violent |
| Ca | burns | steady with cold water; floats as bubbles cling | vigorous |
| Mg | burns with dazzling white flame | hot water; also floats | vigorous |
| Al, Zn | thin protective oxide layer forms | steam only | moderate |
| Fe | filings sparkle in a flame | steam only | moderate |
| Pb | protective layer | none | slow |
| Cu | black coating when heated | none | none — below hydrogen |
| Ag, Au | none, even when hot | none | none |
Ca(s) + 2H2O(l) → Ca(OH)2(aq) + H2(g)
3Fe(s) + 4H2O(g) → Fe3O4(s) + 4H2(g)
Fe(s) + 2HCl(aq) → FeCl2(aq) + H2(g)
3. The reactivity series
Arranging metals in order of decreasing reactivity gives the reactivity series (called the activity series in the US). It is the key to the whole topic: every property above, and every extraction method below, follows from a metal's position.
Figure 1 — The reactivity series. The three colour bands become the three extraction routes in section 7.
Patient Scientists Carefully Mix Acids, Zinc, Iron — Leaving Hydrogen Clouds Making Shiny Gold
Potassium · Sodium · Calcium · Magnesium · Aluminium · Zinc · Iron · Lead · Hydrogen · Copper · Mercury · Silver · Gold
4. Ionic bonding
Noble gases (He, Ne, Ar) do not react because their outer shell is full. Other elements react so as to reach the same stable arrangement — by losing electrons or by gaining them.
Figure 2 — Sodium gives its single outer electron to chlorine. Na+ (2,8) and Cl− (2,8,8) both end with full outer shells.
The oppositely charged ions are held together by strong electrostatic attraction. This is an ionic bond (also called an electrovalent bond), and the compound is an ionic compound.
| Element | Arrangement | Does what | Ion formed |
|---|---|---|---|
| Na (11) | 2, 8, 1 | loses 1 electron | Na+ (2, 8) |
| Mg (12) | 2, 8, 2 | loses 2 electrons | Mg2+ (2, 8) |
| Cl (17) | 2, 8, 7 | gains 1 electron | Cl− (2, 8, 8) |
| O (8) | 2, 6 | gains 2 electrons | O2− (2, 8) |
5. Properties of ionic compounds
| Property | Reason |
|---|---|
| Hard solids, but brittle | strong attraction between oppositely charged ions |
| High melting and boiling points | a lot of energy is needed to overcome that attraction |
| Soluble in water | water is a polar solvent |
| Insoluble in kerosene, petrol | these are non-polar solvents |
| Conduct when molten or dissolved | the ions are free to move |
| Do not conduct as solids | ions are fixed in place and cannot move |
6. Where metals come from — a case study
| Term | Meaning |
|---|---|
| Mineral | a naturally occurring element or compound in the Earth's crust |
| Ore | a mineral from which a metal can be extracted profitably. Every ore is a mineral; not every mineral is an ore. |
| Gangue | earth, sand and rock that come out of the ground mixed with the ore |
Metals at the bottom of the series — gold, silver, platinum — are so unreactive that they occur free (native). Metals at the top never do; they are always locked in compounds.
Textbook extraction can feel abstract. In the state of Rajasthan it is a local industry. According to the state's Department of Mines and Geology, Rajasthan holds India's largest lead-zinc ore resources. [6]
| Site | District | Metals |
|---|---|---|
| Zawar | Udaipur | lead, zinc — one of the oldest mining areas in the world (see Part 2) |
| Rampura-Agucha | Bhilwara | zinc, lead — among the largest zinc mines in the world |
| Rajpura-Dariba | Rajsamand | zinc, lead, silver |
| Khetri | Jhunjhunu | copper, with gold recovered as a by-product [6] |
Why this matters for you: the main zinc ore here is zinc blende, ZnS — a sulfide. That is exactly the ore used in the textbook roasting equation in the next section. When you write 2ZnS + 3O2, you are writing what happens in these furnaces.
7. Extraction
Getting pure metal from ore has three stages: enrichment (removing gangue), reduction (freeing the metal), and refining (purifying it). How the middle stage is done depends entirely on reactivity.
Figure 3 — A metal's reactivity decides its extraction route. The colour bands of Figure 1 have become three pathways.
(a) Low reactivity — heat alone
2Cu2S + 3O2 Δ→ 2Cu2O + 2SO2 then 2Cu2O + Cu2S Δ→ 6Cu + SO2
(b) Medium reactivity — make the oxide, then reduce it
| Process | Used on | Conditions |
|---|---|---|
| Roasting | sulfide ores | strong heating in excess air |
| Calcination | carbonate ores | strong heating in limited air |
Calcination: ZnCO3(s) → ZnO(s) + CO2(g)
Reduction: ZnO(s) + C(s) → Zn(s) + CO(g)
Fe2O3(s) + 2Al(s) → 2Fe(l) + Al2O3(s) + heat
So much heat is released that the iron comes out molten. It is used to weld railway tracks and repair cracked machinery.
(c) High reactivity — electrolysis
Na, Mg, Ca and Al are more reactive than carbon, so carbon cannot reduce their oxides. They are extracted by electrolysis of their molten chlorides (aluminium from its oxide):
8. Refining
Extracted metal still carries impurities. Copper, zinc, tin, nickel, silver and gold are commonly purified by electrolytic refining.
Figure 4 — Impure copper dissolves from the anode; pure copper plates onto the cathode. Soluble impurities stay in solution; insoluble ones fall as anode mud.
9. Corrosion and alloys
What exactly does iron need in order to rust? A classic three-tube experiment answers it (drawn in section 10):
| Tube | Contents | Result |
|---|---|---|
| A | iron nail in ordinary tap water (air present) | rusts |
| B | nail in boiled water under a layer of oil (no air) | no rust |
| C | nail with anhydrous calcium chloride (no moisture) | no rust |
Prevention: painting, oiling or greasing · galvanising (a zinc coating — Rajasthan's zinc at work) · chromium plating · anodising · alloying.
| Alloy | Made of | Why useful |
|---|---|---|
| Stainless steel | iron + nickel + chromium | hard and rust-resistant |
| Brass | copper + zinc | utensils, fittings |
| Bronze | copper + tin | statues, medals |
| Solder | lead + tin | low melting point — joins electrical wires |
| Amalgam | mercury + another metal | any alloy containing mercury |
10. Diagrams to draw
Looking at a diagram and drawing one are different skills. Each diagram below comes with steps. Draw along on paper as you read.
Diagram A — dot-and-cross structure of MgCl2
Diagram A — magnesium's two outer electrons go one each to two chlorine atoms.
- Write Mg on the left with two dots — its outer electrons.
- Write two Cl atoms on the right, each surrounded by seven crosses. Dots and crosses keep the two atoms' electrons distinguishable.
- Draw a curved arrow from each Mg dot to a chlorine.
- After the arrow: [Mg]2+ 2[Cl]−, showing each chloride ion with 8 electrons. Never omit the brackets and charges — half the mark depends on them.
Diagram B — electrolytic refining
The full coloured version is Figure 4 in section 8.
- A wide rectangular tank, with a line for the solution level.
- A thick plate on the left, labelled "anode (+) — impure copper".
- A thin strip on the right, labelled "cathode (−) — pure copper".
- A battery above: anode to the positive terminal, cathode to the negative.
- A heap under the anode — "anode mud"; label the solution "acidified copper(II) sulfate".
Diagram C — conditions for rusting
Diagram C — only the nail in tube A rusts, where both air and water are present.
- Three evenly spaced test tubes with corks, labelled A, B, C.
- A: water half-way. B: water with a thick line for the oil layer on top. C: small granules at the bottom for CaCl2.
- A nail in each. Add small spots on nail A to show rust.
- One line of conclusion under each tube. An unlabelled diagram earns at most half the marks.
11. How examiners award marks
Below is a model answer to a four-mark question, with the marks each part typically attracts. (This illustrates common examiner practice; it is not any board's official mark scheme.)
Question [4 marks]: Describe the electrolytic refining of copper with a labelled diagram.
Labelled diagram — anode, cathode, electrolyte, anode mud, battery terminals. 2 marks
Impure copper is the anode; a thin strip of pure copper is the cathode; acidified copper(II) sulfate is the electrolyte. 1 mark
When current flows, copper dissolves from the anode and an equal amount of pure copper deposits on the cathode. Soluble impurities remain in solution; insoluble ones collect below the anode as anode mud. 1 mark
12. Equation bank
Al2O3 + 6HCl → 2AlCl3 + 3H2O | Al2O3 + 2NaOH → 2NaAlO2 + H2O
2Na + 2H2O → 2NaOH + H2 | Ca + 2H2O → Ca(OH)2 + H2
3Fe + 4H2O → Fe3O4 + 4H2 | Fe + 2HCl → FeCl2 + H2
2HgS + 3O2 → 2HgO + 2SO2 | 2HgO → 2Hg + O2
2Cu2S + 3O2 → 2Cu2O + 2SO2 | 2Cu2O + Cu2S → 6Cu + SO2
2ZnS + 3O2 → 2ZnO + 2SO2 | ZnCO3 → ZnO + CO2 | ZnO + C → Zn + CO
Fe2O3 + 2Al → 2Fe + Al2O3 + heat
13. The trap table
Misconceptions and exam errors, in one place. The left column is what goes wrong; the right is what to do instead.
| The trap | The fix |
|---|---|
| "All metals are hard." | Sodium and potassium cut with a knife. |
| "Non-metals never conduct." | Graphite conducts — that is why it makes electrodes. |
| "Mineral and ore mean the same." | An ore is a mineral that can be mined profitably. |
| Roasting and calcination confused | Roasting: sulfide, excess air. Calcination: carbonate, limited air. State the air. |
| "Ionic compounds always conduct." | Only when molten or dissolved. Always state the state. |
| Only one equation for an amphoteric oxide | Give both — with acid and with base. |
| Anode and cathode swapped in refining | Anode = Adulterated (impure). |
| Brackets and charges missing in dot-and-cross | [Mg]2+ and [Cl]− — half the mark. |
| "Rust needs only water." | Air and water — tube B proves it. |
| "More reactive means corrodes faster." | Aluminium is more reactive than iron but protected by its oxide layer. See challenge Q10. |
14. Questions at three levels
Foundation
Q1 Name the metal that is liquid at room temperature.
Q2 Why is sodium stored under kerosene?
Q3 What is brass made of?
Exam level
Q4 [2 marks] What is an amphoteric oxide? Give an example with both equations.
Q5 [3 marks] Distinguish roasting from calcination, with an equation for each.
Q6 [3 marks] Why do ionic compounds have high melting points? Why do they not conduct as solids?
Q7 [4 marks] Describe electrolytic refining of copper with a labelled diagram.
Challenge
Q8 A sample of zinc blende arrives from a mine. List every stage needed to obtain pure zinc, with equations. Why is carbon used rather than electrolysis?
Q9 Blue copper sulfate solution is left overnight in an iron bucket. What is seen next morning, and why? What if the bucket were silver?
Q10 Aluminium is above iron in the series, so more reactive. Why, then, does an aluminium pan not corrode away like an iron one?
15. Self-test — 15 questions
Answer on paper, then open the answers. 12 or more correct means you are ready.
- Name a lustrous non-metal.
- Name a non-metal that conducts electricity.
- Which metal is the most malleable?
- Name two amphoteric oxides.
- Which metal floats when it reacts with cold water?
- Which metal sits immediately below hydrogen?
- Electron arrangement of Na+?
- What is gangue?
- Which process is used on carbonate ores?
- Give one use of the thermite reaction.
- In refining, what is the cathode made of?
- What two things does rusting need?
- What is stainless steel made of?
- How many parts gold in 22-carat gold?
- What is the main zinc ore in the case study?
16. Glossary
| English | हिन्दी | English | हिन्दी |
|---|---|---|---|
| Malleability | आघातवर्ध्यता | Ore | अयस्क |
| Ductility | तन्यता | Gangue | गैंग |
| Sonorous | ध्वानिक | Roasting | भर्जन |
| Amphoteric | उभयधर्मी | Calcination | निस्तापन |
| Reactivity series | सक्रियता श्रेणी | Refining | परिष्करण |
| Ionic bond | आयनिक बंध | Anode mud | ऐनोड पंक |
| Cation / Anion | धनायन / ऋणायन | Alloy | मिश्रातु |
17. For parents and teachers
- Recite the reactivity series. (Ask for the memory sentence — "Patient Scientists…")
- Why is sodium kept under kerosene? (it ignites in air)
- Why doesn't solid salt conduct? (its ions cannot move)
- What does rusting need? (air and water)
- Draw the refining cell. (check that "impure" is written at the anode)
What follows is for students who want to know why — and to meet two remarkable achievements of ancient Indian metallurgy that modern science has only recently explained.
A. Metallic bonding — why metals behave like metals
Part 1 listed what metals do — shine, bend, conduct. It never said why. The answer is metallic bonding, taught in GCSE and US courses but not in NCERT Class 10. [7]
In a metal, each atom releases its outer electrons into a shared pool. What remains is a regular arrangement of positive ions surrounded by a "sea" of delocalised electrons that belong to no single atom. The attraction between the ions and this sea is the metallic bond. [7]
Figure 5 — The "sea of electrons" model. The electrons wander freely through the whole metal.
| Property from Part 1 | Explained by metallic bonding |
|---|---|
| conducts electricity | the delocalised electrons can drift through the metal and carry charge |
| conducts heat | mobile electrons pass energy along quickly |
| malleable and ductile | layers of ions can slide over one another; the electron sea keeps holding them together, so the metal bends instead of breaking |
B. The Delhi iron pillar — the science
The pillar that opened this guide has puzzled scientists for over a century. The most thorough explanation comes from the late Professor R. Balasubramaniam of the Department of Materials and Metallurgical Engineering, IIT Kanpur, published in the peer-reviewed journal Corrosion Science in 2000. [1]
What he found. The pillar's iron has an unusually high phosphorus content. In the presence of this phosphorus, a compact protective layer forms next to the metal surface — first an amorphous iron oxyhydroxide, and then, crucially, a layer of iron hydrogen phosphate. This film seals the iron beneath it. [1]
The climate helps too. The same study notes that humidity in Delhi rarely stays above about 70 per cent for long periods, and earlier research had shown that atmospheric rusting of iron is not significant below that level. [1]
Link to Part 1. Rusting needs air and water — and the pillar receives both. What protects it is a barrier, exactly the principle behind painting, galvanising, or aluminium's oxide layer in challenge Q10. Ancient Indian smiths produced that barrier through the composition of the iron itself.
C. Zawar — the world's oldest known zinc works
Zawar, in the Udaipur district of the case study in Part 1, has been described in a 2026 peer-reviewed study as the world's oldest known site for zinc mining and smelting, with evidence of mining going back to around 800 BCE. [3] Its systematic excavation was led from the 1980s by a research team including Paul Craddock of the British Museum. [2]
Why zinc is hard to make. In Part 1 you wrote ZnO + C → Zn + CO. It looks simple. The difficulty is that zinc boils at about 907 °C [7] — lower than the temperature needed for carbon to reduce its oxide. So in an ordinary furnace zinc is produced as a vapour, which meets the air and turns straight back into zinc oxide. You make the metal and lose it in the same moment.
The Zawar solution — downward distillation. The ore was sealed in clay retorts that were turned upside down over a cooler chamber. The zinc vapour flowed downward, away from the air, and condensed there as liquid metal. [3]
Figure 6 — A simplified schematic of downward distillation. The key idea: trap the zinc vapour before air can re-oxidise it.
D. Aluminium — and the case for recycling
Part 1 showed that aluminium sits above carbon in the reactivity series, so it cannot be extracted by carbon — it must be won by electrolysis, which consumes enormous amounts of electricity.
That is why recycling matters so much for this particular metal. According to the United States Environmental Protection Agency, recycling aluminium cans saves 95 per cent of the energy required to make the same aluminium from raw ore. [4] The United States Geological Survey notes that aluminium can be recycled over and over without losing its physical properties. [5]
E. Where this leads
| Field | What people do |
|---|---|
| Materials and metallurgical engineering | design alloys, study corrosion — the discipline behind the iron pillar research |
| Archaeometallurgy | reconstruct ancient furnaces and processes, as at Zawar |
| Mining and mineral engineering | locate ores, plan extraction, manage environmental impact |
| Corrosion engineering | protect bridges, pipelines, ships and power plants |
| Recycling and circular economy | recover metals from scrap, electronics and old batteries |
References
Only universities, museum-led research teams, peer-reviewed journals and government agencies are cited. Each link was checked when this guide was written.
- Balasubramaniam, R. "On the corrosion resistance of the Delhi iron pillar." Corrosion Science 42 (2000), 2103–2129. Department of Materials and Metallurgical Engineering, Indian Institute of Technology Kanpur. home.iitk.ac.in
- Craddock, P., Cribb, J., Gale, N. and Gurjar, L. "Sources of zinc in early India: the evidence" (2015). Hosted by the Pennsylvania State University archaeology library. os.pennds.org
- "Preliminary geochemical assessment of ancient zinc smelting retorts in Zawar, Rajasthan: implications for reprocessing potential and environmental concerns." Peer-reviewed article, 2026. sciencedirect.com
- United States Environmental Protection Agency. "Communicating the Benefits of Recycling." archive.epa.gov
- United States Geological Survey, National Minerals Information Center. "Aluminum Statistics and Information." usgs.gov
- Department of Mines and Geology, Government of Rajasthan. Mineral resources of the state. mines.rajasthan.gov.in
- Chemistry LibreTexts — open textbook project hosted by the University of California, Davis. Chapters on metallic bonding and physical data of the elements. chem.libretexts.org
- National Council of Educational Research and Training (NCERT), Government of India. Science — Textbook for Class X. ncert.nic.in
About this guide
Part 1 — curriculum basis. Every fact, equation, definition and example in Part 1 comes from the NCERT Science textbook for Class 10 [8], prescribed by the Board of Secondary Education, Rajasthan, India, for 2026–27. The only additions are the case-study box on Rajasthan's mines, sourced from the state government [6], and the memory sentence and drawing steps, which are study aids. Nothing from Part 2 has been mixed into Part 1.
Part 2 — extension. Not examined at Grade 10. Each section rests on a separate institution so that no single source carries the argument.
Diagrams. All figures are original vector drawings made for this guide, free to view, print and share.
Before your exam, check your own board's specification.

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