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⚛️ Atomic Structure (Q1–4)
1
Atomic Structure
Isotopes of the same element have the same number of:
ANeutrons
BProtons only
CProtons and electrons
DMass numbers
Answer: C — Protons and electrons. Isotopes are atoms of the same element with the same atomic number (same number of protons) but different mass numbers (different numbers of neutrons). Since atoms are neutral, protons = electrons. So isotopes have the same number of protons AND electrons, but different numbers of neutrons. Example: ¹²C and ¹⁴C both have 6 protons and 6 electrons, but 6 and 8 neutrons respectively.
2
Electronic Configuration
An element has the electronic configuration 2,8,6. It is in:
APeriod 3, Group VI
BPeriod 2, Group VI
CPeriod 3, Group II
DPeriod 6, Group III
Answer: A — Period 3, Group VI. The number of electron shells = Period number. 2,8,6 has 3 shells → Period 3. The number of outer-shell electrons = Group number (for Groups I–VII). 6 outer electrons → Group VI. This element is sulfur (S), atomic number 16.
3
Atomic Structure
A sodium ion (Na⁺) has:
A11 protons, 11 electrons
B11 protons, 10 electrons
C10 protons, 11 electrons
D10 protons, 10 electrons
Answer: B — 11 protons, 10 electrons. Sodium (Na) has atomic number 11 → 11 protons (unchanged by ion formation). Na⁺ has lost 1 electron, so 11 − 1 = 10 electrons. The positive charge comes from having more protons than electrons. Proton number is always fixed for an element — only electrons change when ions form.
4
Relative Atomic Mass
Chlorine exists as ³⁵Cl (75%) and ³⁷Cl (25%). The relative atomic mass of chlorine is:
A35.0
B36.0
C35.5
D37.0
Answer: C — 35.5. Relative atomic mass = (mass × abundance) summed for all isotopes. = (35 × 75/100) + (37 × 25/100) = 26.25 + 9.25 = 35.5. The Ar of Cl is 35.5, which is why the periodic table shows a non-integer value — it reflects the weighted average of naturally occurring isotopes.
🔗 Chemical Bonding (Q5–7)
5
Ionic Bonding
Which statement best describes an ionic compound?
AIt has low melting point and does not conduct electricity
BIt has a giant lattice of oppositely charged ions with high melting point
CIt consists of molecules held by weak covalent bonds
DIt conducts electricity when solid
Answer: B. Ionic compounds form giant ionic lattices — a regular 3D arrangement of oppositely charged ions held by strong electrostatic forces. This gives them: high melting/boiling points (much energy needed to break many ionic bonds), ability to conduct when molten or in solution (ions free to move), but NOT when solid (ions fixed in lattice). Examples: NaCl, MgO.
6
Covalent Bonding
Water (H₂O) has a bent molecular shape because:
AOxygen has two lone pairs that repel the bonding pairs
BHydrogen atoms are too small to form a linear molecule
COxygen forms only single bonds
DWater has three atoms so it must be bent
Answer: A. Oxygen in H₂O has 2 bonding pairs (O–H bonds) and 2 lone pairs. Lone pair–lone pair repulsion > lone pair–bonding pair repulsion > bonding pair–bonding pair repulsion. The two lone pairs push the H–O–H angle down to approximately 104.5°, giving a bent/V-shape. Compare with NH₃ (1 lone pair, 3 bonding pairs) which is trigonal pyramidal at ~107°.
7
Metallic Bonding
Metals are good conductors of electricity because they contain:
AMobile ionic bonds
BA sea of delocalised electrons that can move through the structure
CCovalent bonds that carry charge
DPositive ions that migrate toward the cathode
Answer: B. In metallic bonding, metal atoms release their outer electrons into a "sea" of delocalised electrons. These electrons are free to move throughout the metallic lattice when a potential difference is applied, carrying charge and making metals good conductors. The positive metal ions remain fixed in a regular lattice. This also explains why metals are good heat conductors — the mobile electrons transfer kinetic energy.
⚗️ The Mole (Q8–10)
8
Mole Calculations
What is the mass of 2 moles of sulfuric acid, H₂SO₄? (H=1, S=32, O=16)
A49 g
B98 g
C196 g
D294 g
Answer: C — 196 g. Mr of H₂SO₄ = (2×1) + 32 + (4×16) = 2 + 32 + 64 = 98 g/mol. Mass = moles × Mr = 2 × 98 = 196 g. Remember: moles = mass/Mr, so mass = moles × Mr.
9
Percentage Composition
What is the percentage by mass of nitrogen in ammonium nitrate, NH₄NO₃? (N=14, H=1, O=16)
A17.5%
B28%
C35%
D14%
Answer: C — 35%. Mr of NH₄NO₃ = 14 + 4 + 14 + 48 = 80 g/mol. There are 2 nitrogen atoms: 2 × 14 = 28 g of N per mole. % N = (28/80) × 100 = 35%. NH₄NO₃ is widely used as a nitrogen fertiliser because of this high N content.
10
Reacting Masses
In the reaction: 2H₂ + O₂ → 2H₂O. What mass of water is produced from 4 g of hydrogen? (H=1, O=16)
A18 g
B36 g
C9 g
D72 g
Answer: B — 36 g. Mr of H₂ = 2, so 4 g = 4/2 = 2 moles of H₂. From equation: 2 mol H₂ → 2 mol H₂O (1:1 ratio). So 2 mol H₂ produces 2 mol H₂O. Mr of H₂O = 18. Mass = 2 × 18 = 36 g. Always: moles H₂ → use ratio → moles H₂O → mass H₂O.
🧫 Acids, Bases & Salts (Q11–14)
11
Acids and pH
A solution has pH 2. Which best describes this solution?
AWeakly alkaline
BStrongly acidic with high H⁺ concentration
CNeutral
DWeakly acidic
Answer: B — Strongly acidic with high H⁺ concentration. The pH scale runs from 0–14: pH 7 = neutral, pH < 7 = acidic, pH > 7 = alkaline. pH 2 is strongly acidic. A pH of 2 means [H⁺] = 0.01 mol/dm³, which is 10× more concentrated than pH 3. Strong acids like HCl fully dissociate to give high H⁺ concentrations.
12
Neutralisation
Which combination produces the salt potassium sulfate (K₂SO₄)?
AKOH + HCl
BK₂CO₃ + H₂SO₄
CKNO₃ + H₂SO₄
DKCl + NaOH
Answer: B — K₂CO₃ + H₂SO₄. Salt name = metal ion from base + acid anion. Potassium sulfate contains K⁺ (from potassium base) and SO₄²⁻ (from sulfuric acid). K₂CO₃ + H₂SO₄ → K₂SO₄ + H₂O + CO₂. Option A gives KCl (from HCl). The acid determines the anion: HCl → chloride, H₂SO₄ → sulfate, HNO₃ → nitrate.
13
Preparing Insoluble Salts
The best method to prepare barium sulfate (BaSO₄, insoluble) is:
ADirect combination of elements
BTitration of BaO with H₂SO₄
CPrecipitation — mixing BaCl₂ solution with Na₂SO₄ solution
DEvaporation of BaSO₄ solution
Answer: C — Precipitation. Insoluble salts are made by precipitation: mixing two soluble solutions whose ions combine to form the insoluble salt. BaCl₂(aq) + Na₂SO₄(aq) → BaSO₄(s)↓ + 2NaCl(aq). The BaSO₄ precipitates out. Filter, wash with distilled water, dry. You cannot dissolve BaSO₄ and evaporate because it is insoluble. Titration is used for soluble salt preparation from acid + alkali.
14
Strong vs Weak Acids
Ethanoic acid (CH₃COOH) and hydrochloric acid (HCl) are both 0.1 mol/dm³. Which is correct?
ABoth have the same pH and react identically
BEthanoic acid has higher pH; HCl fully dissociates, ethanoic acid partially dissociates
CHCl has higher pH than ethanoic acid
DEthanoic acid is more corrosive than HCl
Answer: B. HCl is a strong acid — it fully (100%) dissociates into H⁺ and Cl⁻. CH₃COOH is a weak acid — it only partially dissociates (≈1% at 0.1 mol/dm³). Same concentration but HCl has much more H⁺ → lower pH. Same concentration of acid neutralises the same amount of alkali (same number of moles), but HCl reacts more vigorously with metals, giving a faster rate.
🔥 Energy Changes (Q15–17)
15
Exothermic / Endothermic
The thermal decomposition of calcium carbonate (CaCO₃ → CaO + CO₂) is:
AExothermic — releases energy to surroundings
BEndothermic — absorbs energy from surroundings
CNeutral — no energy change
DExothermic in the forward direction only
Answer: B — Endothermic. Thermal decomposition reactions require a continuous supply of heat → endothermic. Energy is absorbed from the surroundings to break the bonds in CaCO₃ (the energy input to break bonds exceeds the energy released forming CaO and CO₂). The temperature of the reaction vessel would fall if the heat supply were removed. Endothermic: ΔH is positive; reactants are at lower energy than products.
16
Bond Energy
Which process always releases energy?
ABreaking covalent bonds
BForming covalent bonds
CDissolving an ionic solid in water
DEvaporating a liquid
Answer: B — Forming covalent bonds. Bond breaking is always endothermic (absorbs energy). Bond forming is always exothermic (releases energy). A reaction is exothermic overall if energy released forming new bonds > energy absorbed breaking old bonds. Options C and D are not always exothermic: some ionic compounds absorb heat on dissolving (endothermic dissolution), and evaporation always absorbs energy.
17
Enthalpy Profile
In an energy profile diagram, activation energy is defined as:
AThe energy of the products
BThe difference between products and reactants energy
CThe minimum energy that colliding particles must have for a reaction to occur
DThe total energy released by the reaction
Answer: C. Activation energy (Ea) is the minimum energy that colliding particles must possess for a reaction to occur — it is the energy required to start breaking the bonds in the reactants. On an energy profile, it is the energy difference between the reactants and the top of the energy "hill" (transition state). A catalyst lowers Ea by providing an alternative reaction pathway. ΔH is the difference between reactant and product energy levels.
📈 Rate of Reaction (Q18–21)
18
Measuring Rate
In the reaction of marble chips with HCl, which variable best measures the rate of reaction?
AThe temperature of the acid
BThe mass of marble chips used
CThe volume of CO₂ gas produced per unit time
DThe colour of the solution
Answer: C — Volume of CO₂ per unit time. Rate = change in quantity / time. Measuring the volume of CO₂ produced at regular time intervals gives a direct measurement of the reaction rate. Alternatively, loss in mass (as CO₂ escapes) can be measured. Temperature and mass of marble are independent variables, not measurements of rate. The faster CO₂ is produced, the steeper the gradient on a volume-vs-time graph.
19
Pressure and Rate
Increasing the pressure of a gaseous reaction increases the rate because:
AGas molecules gain more energy at higher pressure
BHigher pressure decreases activation energy
CMolecules are closer together so collision frequency increases
DPressure increases the temperature of the gas
Answer: C. Increasing pressure compresses the gas — molecules are forced into a smaller volume, so they are closer together. This increases the number of collisions per unit time (collision frequency), leading to more successful collisions per second and a faster rate. Pressure does not change activation energy or give particles more energy (that would require a temperature increase).
20
Catalyst
Which statement about a heterogeneous catalyst is correct?
AIt is in the same physical state as the reactants
BIt is consumed during the reaction
CIt is in a different physical state from the reactants and works at its surface
DIt increases the activation energy
Answer: C. A heterogeneous catalyst is in a different physical state from the reactants. Example: iron catalyst (solid) in the Haber process with N₂ and H₂ gases. Reactants adsorb onto the catalyst surface, where bonds are weakened and reaction occurs more easily. The catalyst is not consumed — it can be recovered unchanged. It lowers (not increases) activation energy. A homogeneous catalyst is in the same state as the reactants.
21
Rate Graph Interpretation
In a rate experiment, the volume–time graph levels off (becomes horizontal) because:
AThe temperature has dropped
BThe catalyst has been used up
COne or more reactants have been completely used up (limiting reagent)
DThe activation energy has increased
Answer: C — Reactant(s) used up. When a limiting reagent is completely consumed, the reaction stops. No more product forms → the volume graph becomes flat. The final volume reached is the same regardless of how fast the reaction was — changing concentration or temperature changes the gradient (speed) but not the final volume (total product), as long as the same amount of limiting reagent is used.
⚙️ Metals & Reactivity (Q22–24)
22
Reactivity Series
Which metal reacts most vigorously with cold water?
AIron
BCopper
CZinc
DPotassium
Answer: D — Potassium. The reactivity series (most to least reactive): K, Na, Ca, Mg, Al, Zn, Fe, Sn, Pb, Cu, Ag, Au. Only metals above Mg react with cold water (K, Na, Ca). K reacts explosively, Na vigorously, Ca slowly. Mg reacts very slowly with cold water but quickly with steam. Zn and Fe react with steam only. Cu does not react with water at all.
23
Alloys
Stainless steel is an alloy of iron and chromium. Alloys are generally harder than pure metals because:
AAlloying creates ionic bonds between the metals
BDifferent-sized atoms disrupt the regular arrangement, preventing layers from sliding
CAlloying increases the number of delocalised electrons
DThe alloy has a lower melting point than pure iron
Answer: B. In pure metals, layers of atoms of the same size can slide over one another easily (making the metal malleable/ductile). In an alloy, atoms of a different size (e.g. Cr in Fe) distort the regular lattice — the layers can no longer slide as easily, making the alloy harder and stronger. This is why alloys like bronze, brass, and stainless steel are more useful than pure metals for structural applications.
24
Extracting Metals
Gold is found as the native (uncombined) element in the Earth's crust because:
AGold is too reactive to form compounds
BGold is very unreactive and does not easily form compounds with other elements
CGold has a very high melting point
DGold reacts with water to form an oxide
Answer: B. Gold is at the very bottom of the reactivity series — it is extremely unreactive. It does not react with oxygen, water, or dilute acids under normal conditions, so it is stable as the free element in nature. Very unreactive metals (Pt, Au, Ag to some extent) are found as native elements. Highly reactive metals (Na, K, Ca) are always found as compounds (oxides, chlorides, etc.).
⚡ Electrolysis & Redox (Q25–27)
25
Electrolysis — Copper Purification
During electrolytic purification of copper, the impure copper is used as the:
ACathode; it gains copper
BAnode; it dissolves, releasing Cu²⁺ ions
CElectrolyte solution
DCathode; it dissolves slowly
Answer: B — Anode; it dissolves. In copper purification: impure copper = anode (+), pure copper = cathode (−), CuSO₄ solution = electrolyte. At anode: Cu → Cu²⁺ + 2e⁻ (impure copper oxidised/dissolves). At cathode: Cu²⁺ + 2e⁻ → Cu (pure copper deposited). Impurities (Zn, Fe) also dissolve but Cu²⁺ is preferentially deposited. Precious metal impurities (Ag, Au) fall as anode sludge.
26
Oxidation States
In the compound Fe₂O₃, what is the oxidation state of iron?
A+2
B+3
C−2
D+6
Answer: B — +3. In Fe₂O₃: oxygen is always −2. Total charge from 3 oxygen atoms = 3 × (−2) = −6. The compound is neutral so 2 Fe atoms must contribute +6 total. Oxidation state of Fe = +6 ÷ 2 = +3. This is iron(III) oxide. Compare with FeO where Fe is +2 (iron(II) oxide). Iron commonly exists in +2 and +3 states — the Roman numeral in the name tells you the oxidation state.
27
Redox Identification
In the reaction: Cl₂ + 2KBr → 2KCl + Br₂. Which statement is correct?
ABr⁻ is oxidised; Cl₂ is the reducing agent
BCl₂ is reduced; Br⁻ is oxidised; Cl₂ is the oxidising agent
CCl₂ is oxidised and Br⁻ is reduced
DNo redox occurs — this is a precipitation reaction
Answer: B. Cl₂ + 2e⁻ → 2Cl⁻ (Cl₂ GAINS electrons → REDUCED). 2Br⁻ → Br₂ + 2e⁻ (Br⁻ LOSES electrons → OXIDISED). OIL RIG. Cl₂ is the oxidising agent (it causes Br⁻ to be oxidised while itself being reduced). This is a halogen displacement reaction — Cl₂ is more reactive than Br₂, so Cl₂ displaces Br⁻ from its salt. The solution turns orange-brown as Br₂ forms.
🛢️ Organic Chemistry (Q28–30)
28
Homologous Series
Which is a member of the alkane homologous series?
AC₂H₄
BC₃H₈
CC₂H₅OH
DCH₃COOH
Answer: B — C₃H₈ (propane). Alkanes have the general formula CₙH₂ₙ₊₂. C₃H₈: n=3, 2(3)+2=8 ✓. Check others: C₂H₄ = C₂H₂(2)+0 → this fits CₙH₂ₙ (alkene formula), it is ethene. C₂H₅OH is ethanol (alcohol). CH₃COOH is ethanoic acid. Alkanes are saturated (only C–C and C–H single bonds), chemically unreactive except for combustion and substitution in UV light.
29
Fermentation
During fermentation, glucose is converted to ethanol. The other product is:
AOxygen
BWater
CCarbon dioxide
DMethane
Answer: C — Carbon dioxide. Fermentation: C₆H₁₂O₆ → 2C₂H₅OH + 2CO₂. Conditions: yeast (enzyme), warm temperature (~30°C), absence of oxygen (anaerobic). CO₂ is the other product — it causes the dough to rise in bread-making and is responsible for bubbles in alcoholic drinks. Fermentation is an alternative to cracking for producing ethanol, though it gives a lower concentration (≈15% max before yeast is killed).
30
Cracking
Cracking of long-chain alkanes produces:
AOnly shorter alkanes
BShorter alkanes and alkenes
COnly alkenes and water
DPolymers and hydrogen
Answer: B — Shorter alkanes and alkenes. Cracking breaks C–C bonds in long-chain alkanes using high temperature and a catalyst (or high temperature alone — thermal cracking). Products are shorter alkane chains AND alkenes (which contain C=C double bonds). Example: C₁₅H₃₂ → C₈H₁₈ + C₅H₁₀ + C₂H₄. The alkenes produced are valuable as monomers for polymerisation (e.g. ethene → poly(ethene)). Cracking converts less useful heavy fractions into more valuable petrol/naphtha fractions.
🌍 Atmosphere & Environment (Q31–33)
31
Greenhouse Effect
Carbon dioxide contributes to the greenhouse effect because:
AIt absorbs UV radiation from the Sun
BIt reflects all sunlight back into space
CIt absorbs infrared radiation re-emitted from the Earth's surface and re-radiates it, trapping heat
DIt decomposes the ozone layer
Answer: C. The greenhouse effect: solar (short-wave) radiation passes through CO₂ to warm the Earth's surface. The Earth re-emits longer-wave infrared (heat) radiation. CO₂ (and CH₄, H₂O, N₂O) absorb this IR and re-radiate it in all directions, including back toward Earth — trapping heat. This natural effect keeps Earth warm enough for life; the problem is enhanced greenhouse effect from burning fossil fuels increasing CO₂ levels. CFCs (not CO₂) damage the ozone layer.
32
Acid Rain
Acid rain is mainly caused by:
ACO₂ dissolving in rain to form carbonic acid
BSO₂ and NOₓ dissolving in rain to form sulfuric and nitric acids
COzone reacting with water
DParticulates from car exhausts
Answer: B. Acid rain: SO₂ (from burning sulfur-containing fossil fuels, volcanoes) + H₂O → H₂SO₃/H₂SO₄. NOₓ (from high-temperature combustion in engines/lightning) + H₂O → HNO₃. Normal rain is slightly acidic (pH ~5.6) due to CO₂, but acid rain has pH 4–5 or lower. Effects: damages buildings (especially limestone/marble), kills aquatic life, leaches nutrients from soil. Prevention: catalytic converters, flue gas desulfurisation, renewable energy.
33
Haber Process
In the Haber process (N₂ + 3H₂ ⇌ 2NH₃), the conditions used are 450°C and 200 atm with an iron catalyst. The temperature of 450°C is chosen because:
AIt maximises the yield of NH₃
BIt is a compromise — higher temperature reduces yield but gives an acceptable rate
CThe catalyst only works at exactly 450°C
DLower temperatures would decompose the NH₃
Answer: B — A compromise. The forward reaction (N₂ + 3H₂ → 2NH₃) is exothermic. By Le Chatelier's principle: lower temperature favours the forward reaction (more NH₃). BUT at low temperature, the rate is too slow. 450°C is a compromise: yield is only ~15% but the rate is fast enough to be economically viable. The unreacted N₂ and H₂ are recycled. High pressure (200 atm) increases yield (fewer moles of gas on the right) AND rate.
🔍 Qualitative Analysis (Q34–36)
34
Cation Tests — NaOH
A solution is tested with NaOH solution. A white precipitate forms that dissolves in excess NaOH. The cation present is:
AFe²⁺
BCu²⁺
CAl³⁺
DZn²⁺
Answer: C — Al³⁺. Both Al³⁺ and Zn²⁺ form white precipitates with NaOH that dissolve in excess (amphoteric hydroxides). However, the standard O-Level test distinguishes them: Al(OH)₃ dissolves in excess NaOH (forming aluminate, Al(OH)₄⁻). Zn(OH)₂ also dissolves in excess NaOH (forming zincate). To distinguish: use NH₃ solution — Zn(OH)₂ dissolves in excess NH₃ but Al(OH)₃ does not. Fe²⁺ → green ppt, Fe³⁺ → brown ppt, Cu²⁺ → blue ppt (none dissolve in excess NaOH).
35
Anion Test — Carbonate
To test for carbonate ions (CO₃²⁻), you add dilute acid and then pass the gas through:
ABromine water
BAcidified potassium manganate(VII)
CLimewater, which turns milky
DDamp red litmus paper
Answer: C — Limewater, which turns milky. CO₃²⁻ + 2H⁺ → CO₂ + H₂O. The CO₂ produced is passed through limewater [Ca(OH)₂ solution]: CO₂ + Ca(OH)₂ → CaCO₃ + H₂O. The white CaCO₃ precipitate makes the limewater turn milky. This is the standard test for CO₂. Bromine water tests for alkenes (decolourised). Acidified KMnO₄ tests for reducing agents/alkenes. Damp red litmus turning blue tests for NH₃.
36
Gas Tests
A gas bleaches damp litmus paper. The gas is most likely:
AHydrogen
BChlorine
CAmmonia
DOxygen
Answer: B — Chlorine. Chlorine (Cl₂) first turns damp red litmus blue (it dissolves in water to form HCl + HOCl; the HOCl is alkaline briefly) then bleaches it completely white. This bleaching is the definitive test for Cl₂. Cl₂ dissolves in water: Cl₂ + H₂O ⇌ HCl + HOCl. HOCl (hypochlorous acid) is the bleaching agent. Ammonia turns damp red litmus blue but does NOT bleach. H₂ causes squeaky pop, O₂ relights glowing splint.
📊 Periodic Table & Mixed Topics (Q37–40)
37
Group I — Alkali Metals
Going down Group I (Li → Na → K), which trend is correct?
AReactivity decreases; melting point increases
BReactivity increases; melting point decreases
CReactivity decreases; atomic radius decreases
DReactivity increases; melting point increases
Answer: B — Reactivity increases; melting point decreases. Down Group I: more electron shells → outer electron further from nucleus → shielded by more inner shells → weaker nuclear attraction → outer electron lost more easily → higher reactivity. Melting/boiling points DECREASE down Group I (weaker metallic bonding as atomic radius increases). Li: mp 181°C, Na: 98°C, K: 63°C. K reacts explosively with water; Li reacts gently — reactivity increases down the group.
38
Group VII — Halogens
Fluorine is more reactive than chlorine because:
AFluorine has more electrons than chlorine
BFluorine has a smaller atomic radius and gains an electron more readily
CFluorine has a lower boiling point
DFluorine has a higher atomic mass
Answer: B. Halogens react by gaining an electron (oxidising agents). Going UP Group VII (towards fluorine): smaller atomic radius → outer shell closer to nucleus → less electron shielding → stronger attraction for an incoming electron → electron gained more easily → higher reactivity. F is the most reactive non-metal known. Reactivity of halogens DECREASES down the group: F > Cl > Br > I.
39
Group 0 — Noble Gases
Noble gases are unreactive because:
AThey have very high boiling points
BThey have full outer electron shells and do not need to gain or lose electrons
CTheir atoms are too small to react
DThey have very high ionisation energies and low atomic masses
Answer: B — Full outer electron shells. Noble gases (He: 2 electrons; Ne, Ar, Kr, Xe: 8 outer electrons) have complete outer electron shells. They have no tendency to gain, lose, or share electrons — therefore do not form bonds under normal conditions. This stability makes them inert. Uses rely on this inertness: He in balloons (non-flammable), Ar in welding (prevents oxidation), Ne in advertising signs (glows when current flows).
40
Transition Metals
Which property is characteristic of transition metals but NOT of Group I metals?
AThey are all solid at room temperature
BThey form coloured compounds and can act as catalysts
CThey conduct electricity
DThey have metallic bonding
Answer: B — Coloured compounds and catalytic activity. Transition metals form coloured compounds (Cu²⁺ = blue, Fe³⁺ = yellow/brown, Fe²⁺ = green, Cr³⁺ = green, MnO₄⁻ = purple) because of incomplete d-subshells. They also act as catalysts (Fe in Haber process, Pt/Pd/Rh in catalytic converters, MnO₂ decomposing H₂O₂). Group I metals form mostly white/colourless compounds and are not typically catalysts. Both groups are solids (except Hg), conduct electricity, and have metallic bonding.