Q.Metallic radii of some transition elements are given below. Which of these elements will have highest density?
Element: Fe, Co, Ni, Cu
Metallic radii/pm: Fe =126, Co =125, Ni =125, Cu =128
Concept understanding — Ionization Energy Trends
Ionization Energy: The First Meeting
Imagine you're holding onto something precious — say, a favourite pen. How hard would someone have to pull to take it from your hand? That's the core idea behind ionization energy. In an atom, the "something precious" is an electron, and the "pulling force" is energy.
Ionization energy (IE) is the minimum energy required to remove the most loosely bound electron from a gaseous atom in its ground state.
Why "gaseous" and "ground state"? Because we want a fair comparison — no extra energy from neighbours or from the atom being already excited. We measure how tightly the atom holds its outermost electron when it's alone and calm.
The unit you'll see most often in exams: kJ/mol (kilojoules per mole of atoms).
The Intuition: What Controls the Grip?
Two factors decide how hard an atom holds its outermost electron:
-
Nuclear charge — more protons in the nucleus means a stronger pull on the electron. Simple: bigger positive charge, tighter grip.
-
Distance from the nucleus — the farther the electron is, the weaker the pull. Think of a magnet: it holds a paperclip strongly up close, but barely at arm's length.
But there's a subtle twist: shielding (or screening). Inner electrons partially block the nuclear charge from reaching the outer electron. The outermost electron doesn't "feel" the full nuclear charge — it feels only the effective nuclear charge (Zeff).
Zeff=Z−S, where Z is the atomic number and S is the shielding constant (roughly the number of inner electrons). This is the net positive charge pulling on the outer electron.
So the real question becomes: How large is Zeff for the outermost electron, and how far away is it?
The Precise Trend: Across a Period
As you move left to right across a period (say, from Li to Ne in period 2):
- Nuclear charge increases steadily (more protons).
- Electrons are added to the same shell — no new inner layers.
- Shielding stays roughly constant (same number of inner electrons).
- Result: Zeff increases → the outer electron is pulled in tighter → ionization energy increases.
Across a period: IE increases (generally).
Example:
Li (IE = 520 kJ/mol) → Be (900) → B (801) → C (1086) → N (1402) → O (1314) → F (1681) → Ne (2081)
Wait — why does B have lower IE than Be? And O lower than N? That's the exception, not the rule. We'll come back to it.
The Precise Trend: Down a Group
As you move down a group (say, from Li to Cs in group 1):
- Nuclear charge increases (more protons).
- But electrons are added to new, higher shells — the outermost electron is much farther from the nucleus.
- Shielding also increases significantly (more inner electrons).
- Result: distance dominates → the outer electron is held more loosely → ionization energy decreases.
Down a group: IE decreases.
Example:
Li (520) → Na (496) → K (419) → Rb (403) → Cs (376) — all in kJ/mol.
The Two Exceptions (and Why They Matter)
Exception 1: Group 13 vs Group 2 (e.g., B vs Be)
Be has a full 2s2 subshell. B has 2s22p1. The 2p electron is slightly higher in energy and slightly better shielded by the 2s electrons than the 2s electrons shield each other. So removing the 2p electron from B takes less energy than removing a 2s electron from Be.
Don't memorise "IE increases across a period" blindly. Group 13 always has lower IE than Group 2 in the same period.
Exception 2: Group 16 vs Group 15 (e.g., O vs N)
N has a half-filled 2p3 subshell — each 2p orbital has one electron. This is an especially stable arrangement (exchange energy stabilisation). O has 2p4 — one orbital gets a second electron. That extra electron experiences electron-electron repulsion, making it easier to remove. So O has lower IE than N.
| Period | Group 15 (IE) | Group 16 (IE) | Which is higher? |
|--------|--------------|--------------|------------------|
| 2 | N (1402) | O (1314) | N > O |
| 3 | P (1012) | S (1000) | P > S |
| 4 | As (947) | Se (941) | As > Se |
The pattern holds for all periods.
The Big Picture: What You Must Remember
Ionization energy increases across a period (with two dips) and decreases down a group.
The dips occur at Group 13 (lower than Group 2) and Group 16 (lower than Group 15).
The underlying reason is always the same: effective nuclear charge and distance. When Zeff is high and the electron is close, IE is high. When the electron is far or repulsion helps it leave, IE is low.
A Final Check: First vs Second Ionization Energy
Removing one electron from an atom leaves a positive ion. Removing a second electron from that ion is always harder — the ion has a higher positive charge pulling on the remaining electrons.
Second IE > First IE — always. For example, Na: first IE = 496 kJ/mol, second IE = 4562 kJ/mol. That's nearly 10 times larger. This huge jump tells you that the second electron comes from a different shell (closer to the nucleus).
In exams, this jump is used to identify the group of an element — a sudden large increase in successive ionization energies indicates you've stripped off all valence electrons and are now pulling from a core shell.
"Ionization energy trends periodic table" and "periodicity class 11 chemistry important questions" are extremely common searches, both anchored in the Classification of Elements and Periodicity chapter of the NCERT/CBSE Class 11 Chemistry curriculum. The Group 13 and Group 16 exceptions in particular are a favourite trap question in board exams and JEE Main.
Why this formula?
Ionization Energy Trends: The Why Behind the Trends
Ionization energy (IE) is the minimum energy required to remove the most loosely bound electron from a gaseous atom in its ground state.
It is measured in kJ/mol or eV/atom.
The key trend is:
IE increases across a period (left → right) and decreases down a group (top → bottom).
But why? Let’s break down the reasoning step-by-step.
1. The Core Formula: Coulomb’s Law
The energy needed to remove an electron is fundamentally governed by the electrostatic attraction between the electron and the nucleus.
F=r2k⋅Zeff⋅e2
Where:
- Zeff = effective nuclear charge (net positive charge felt by the electron)
- r = distance of the electron from the nucleus
- e = charge of electron
- k = Coulomb constant
Key insight: The stronger the attraction, the higher the ionization energy.
2. Why IE Increases Across a Period
Reasoning:
- As you move left → right, protons increase in the nucleus.
- Electrons are added to the same principal energy level (same shell).
- Shielding by inner electrons remains roughly constant (same number of inner shells).
- Therefore, Zeff increases — the outer electrons feel a stronger pull.
Result:
IE∝Zeff
So IE increases across a period.
Example:
- Na (Z=11): IE = 496 kJ/mol
- Mg (Z=12): IE = 738 kJ/mol
- Al (Z=13): IE = 578 kJ/mol (slight dip due to p-orbital shielding — see exception below)
3. Why IE Decreases Down a Group
Reasoning:
- As you move down a group, principal quantum number n increases.
- The outermost electron is farther from the nucleus (r increases).
- Shielding increases because more inner electron shells are present.
- Zeff increases only slightly (not enough to compensate for distance).
Result:
IE∝r21
So IE decreases down a group.
Example:
- Li (n=2): IE = 520 kJ/mol
- Na (n=3): IE = 496 kJ/mol
- K (n=4): IE = 419 kJ/mol
4. The Mathematical Expression (Approximation)
For a hydrogen-like atom (single electron), the ionization energy is given by:
IE=n213.6eV⋅Z2
For multi-electron atoms, we replace Z with Zeff:
IE≈n213.6eV⋅Zeff2
Why this holds:
- Zeff accounts for shielding by inner electrons.
- n is the principal quantum number of the electron being removed.
- The 1/n2 dependence comes from the Bohr model — energy levels scale as En∝−Z2/n2.
5. Exceptions (Why the Trend Isn’t Perfect)
a) Group 13 vs Group 2 (e.g., Al vs Mg)
- Al has a p-orbital electron (higher energy, easier to remove) than Mg’s s-orbital.
- Also, p-orbitals are more shielded by s- and p-electrons.
b) Group 16 vs Group 15 (e.g., O vs N)
- N has a half-filled p-subshell (extra stability).
- O has one paired electron — electron-electron repulsion makes removal easier.
6. Summary Table
| Factor | Across Period (→) | Down Group (↓) |
|---|---|---|
| Zeff | Increases | Increases slightly |
| r (distance) | Decreases slightly | Increases |
| Shielding | Constant | Increases |
| IE | Increases | Decreases |
Final Takeaway
Ionization energy is not just a number — it’s a direct consequence of Coulomb’s law, modified by shielding and orbital shape.
The trend is driven by Zeff (across) and distance + shielding (down).
Always ask: “How strongly is this electron held?” — and the answer lies in the balance of nuclear charge, distance, and shielding.
Concept: Density depends on mass per unit volume. For metals in the same period, atomic mass increases faster than atomic volume, so density generally increases across a series.
Reasoning:
- Density ∝atomic volumeatomic mass. Atomic volume ∝(radius)3.
- Atomic masses (approx.): Fe = 55.8, Co = 58.9, Ni = 58.7, Cu = 63.5 g/mol.
- Radii: Fe = 126, Co = 125, Ni = 125, Cu = 128 pm. Volume scales as r3, so Cu has the largest volume, but its mass is significantly higher.
- Compare mass/volume ratios: Cu has the highest atomic mass with only a slightly larger radius, giving it the greatest density.
The element with the highest density is Cu (option (iv)).
Density depends on atomic mass and atomic volume (radius³). Among Fe, Co, Ni, and Cu, copper has the highest atomic mass and a relatively large radius, giving it the highest density.
Why density depends on radius and mass
Density is mass per unit volume. For a metallic crystal, the density of the element is proportional to:
Density∝(Metallic radius)3Atomic mass
The exact formula involves packing fraction and Avogadro’s number, but for comparing elements with the same crystal structure (all four are face-centered cubic at room temperature), the packing fraction cancels out. So we only need to compare:
r3Atomic mass
A higher atomic mass and a smaller radius both push density up. Let’s see which element wins.
Step-by-step comparison
1. List the given data
| Element | Metallic radius (pm) | Atomic mass (g/mol) |
|---|---|---|
| Fe | 126 | 55.85 |
| Co | 125 | 58.93 |
| Ni | 125 | 58.69 |
| Cu | 128 | 63.55 |
The radii are nearly equal — all within 3 pm of each other. So the atomic mass will be the deciding factor.
2. Compute M/r3 for each
We can work with relative values since the constant factor (packing fraction, Avogadro’s number) is the same for all.
For Fe:
126355.85=200037655.85≈2.79×10−5
For Co:
125358.93=195312558.93≈3.02×10−5
For Ni:
125358.69≈3.00×10−5
For Cu:
128363.55=209715263.55≈3.03×10−5
3. Compare the values
- Fe: 2.79×10−5 — lowest, because Fe has the smallest atomic mass and a mid-sized radius.
- Co: 3.02×10−5 — higher than Fe.
- Ni: 3.00×10−5 — very close to Co, slightly lower.
- Cu: 3.03×10−5 — the highest value.
Copper’s atomic mass is about 7–8% higher than cobalt’s, and its radius is only 2.4% larger. The cube in the denominator means a 2.4% radius increase raises the volume by about 7.4%, but the mass increase of ~7.8% more than compensates. So Cu edges ahead.
You don’t need to compute the exact numbers. Just compare ratios:
For Co vs Cu: 125358.93 vs 128363.55.
Notice 128/125=1.024, so (128/125)3≈1.074.
The mass ratio 63.55/58.93≈1.078. Since 1.078>1.074, Cu wins.
4. Final ranking
Cu > Co > Ni > Fe in density.
A common mistake is to pick the element with the smallest radius (Co or Ni) thinking that smaller radius always means higher density. But density also depends on atomic mass — copper is heavier enough to overcome its slightly larger radius.
The element with the highest density is (iv) Cu.
Method: Density Estimation from Metallic Radius and Atomic Mass
This problem uses the relationship between density, atomic mass, and atomic radius in a periodic table trend context.
Concept Behind the Method
Density (ρ) is mass per unit volume. For metallic elements in the same period:
- Mass depends on atomic mass (increases across a period)
- Volume depends on atomic radius (generally decreases across a period)
Since density ∝volumemass, and volume ∝r3, we can compare density using:
ρ∝r3Atomic mass
Steps to Solve
Step 1: List the given data
| Element | Metallic radius (pm) | Atomic mass (g/mol) |
|---|---|---|
| Fe | 126 | 55.85 |
| Co | 125 | 58.93 |
| Ni | 125 | 58.69 |
| Cu | 128 | 63.55 |
Step 2: Calculate r3 for each element
- Fe: 1263=2,000,376
- Co: 1253=1,953,125
- Ni: 1253=1,953,125
- Cu: 1283=2,097,152
Step 3: Compute r3Atomic mass for comparison
- Fe: 2,000,37655.85≈2.79×10−5
- Co: 1,953,12558.93≈3.02×10−5
- Ni: 1,953,12558.69≈3.00×10−5
- Cu: 2,097,15263.55≈3.03×10−5
Step 4: Compare the values
The highest value indicates the highest density.
Order: Cu > Co > Ni > Fe
Final Answer
Cu has the highest density.
(iv) Cu
Why This Works
Across the first transition series, atomic mass increases steadily while atomic radius remains nearly constant (due to poor shielding by d-electrons). Copper has the highest atomic mass among these four, with only a slightly larger radius — giving it the highest density.
Common Mistakes & How to Avoid Them
Mistake 1: Assuming the smallest radius always gives the highest density
Why students make it:
They see Co and Ni have the smallest radii (125 pm) and assume "smaller atom = more tightly packed = denser," picking (iii) Co or (ii) Ni without checking atomic mass.
Why it's wrong:
Density depends on mass per unit volume, not radius alone. A smaller radius does increase density for a fixed mass, but here the atomic masses are also different — and that difference decides the outcome.
How to avoid:
Always write the formula:
Density∝Atomic volumeAtomic mass
For a spherical atom, volume ∝r3. So:
Density∝r3Atomic mass
Check the numbers:
| Element | Atomic mass (g/mol) | Radius (pm) | r3 (× 106 pm³) | Mass/r3 (relative) |
|---|---|---|---|---|
| Fe | 55.85 | 126 | 2.00 | 27.9 |
| Co | 58.93 | 125 | 1.95 | 30.2 |
| Ni | 58.69 | 125 | 1.95 | 30.1 |
| Cu | 63.55 | 128 | 2.10 | 30.3 |
Result: Cu has the highest mass per unit volume → highest density, even though its radius is the largest of the four — its atomic mass is high enough to overcome the larger volume.
Correct answer: (iv) Cu
Mistake 2: Forgetting that density depends on atomic mass, not just radius
Why students make it:
They focus only on the given radii and ignore the atomic masses (which are not directly given but must be recalled from periodic table knowledge).
How to avoid:
Always recall or note the atomic masses of the elements in the series. For 3d transition series:
- Fe ≈ 56
- Co ≈ 59
- Ni ≈ 58.7
- Cu ≈ 63.5
Cu has both the largest radius and the largest mass among these four — so the ratio, not either number alone, decides the answer.
Mistake 3: Thinking density tracks radius alone across the series
Why students make it:
They remember that atomic radii change only slightly across Fe–Co–Ni–Cu, so they assume the element with the smallest radius must be densest.
Why it's wrong:
Across the 3d series, density is set by the combination of mass and volume. Cu's radius is about 2.4% larger than Co's/Ni's, which raises its volume by about 7.4% — but Cu's atomic mass is about 7.8% higher than Co's, which more than compensates.
How to avoid:
Compare ratios directly instead of eyeballing radius or mass alone:
- Fe → Co: mass ↑ noticeably, radius ↓ slightly → density increases
- Co → Ni: mass and radius both nearly unchanged → density nearly the same
- Ni → Cu: mass ↑ more than radius ↑ → density increases again, reaching its highest value at Cu
So the peak is at Cu, not Co.
Mistake 4: Confusing metallic radius with density formula
Why students make it:
They try to use the metallic radius directly in density without converting to volume.
How to avoid:
Remember: density uses volume, which scales as r3. A 2% change in radius causes ~6-7% change in volume — significant enough to matter here.
Quick Summary — Do This Instead
| Step | Action |
|---|---|
| 1 | Note atomic masses (from memory or periodic table) |
| 2 | Compute r3 for each element |
| 3 | Compute mass/r3 (relative comparison is enough) |
| 4 | Pick the largest ratio |
Final answer: (iv) Cu
- KEAM 2026Set eng-2026-04184 marksMCQQ.The correct decreasing order of the first ionization enthalpies among the elements C, N, O, F is (A) N > O > F > C (B) O > F > N > C (C) C > N > O > F (D) F > N > O > C (E) C > O > N > F
›Reveal solutionSolution
The order is F>N>O>C; nitrogen's stable half-filled 2p3 configuration gives it a higher first IE than oxygen.
Generally first ionization enthalpy increases across a period (C < N < O < F), but the extra-stable half-filled 2p3 of nitrogen makes it harder to ionize than oxygen (whose paired 2p4 electron is easier to remove).
Approximate values (kJ mol⁻¹): C ≈ 1086, N ≈ 1402, O ≈ 1314, F ≈ 1681.
Decreasing order:
F>N>O>C
✓Final answerThe correct option is (D).
- KEAM 2026Set eng-2026-04224 marksMCQQ.Which of the following represents the correct increasing order of first ionization enthalpy for Ca, Ba, S, Se and Ar? (A) Ca < S < Ba < Se < Ar (B) Ar < S < Ba < Se < Ca (C) Ba < Ca < Se < S < Ar (D) Ba < Ca < S < Se < Ar (E) Ca < S < Ar < Se < Ba
›Reveal solutionSolution
First ionization enthalpies rise across a period and fall down a group: Ba < Ca < Se < S < Ar.
Approximate IE1 values (kJ/mol): Ba ≈ 503, Ca ≈ 590, Se ≈ 941, S ≈ 1000, Ar ≈ 1521. Ba is below Ca in group 2 (lower IE); S is above Se in group 16 (higher IE); Ar, a noble gas, is highest. Increasing order: Ba < Ca < Se < S < Ar.
✓Final answerThe correct option is (C).
- KEAM 2025Set eng-2025-04274 marksMCQQ.The alkali metal with the highest first enthalpy of ionization is (A) Cs (B) Rb (C) K (D) Na (E) Li
›Reveal solutionSolution
Down Group 1, atomic size increases and the outer electron is less tightly held, so ionization enthalpy falls — making Li the highest and Cs the lowest.
Among the alkali metals (Li, Na, K, Rb, Cs), the first ionization enthalpy decreases down the group. As we move down, the atomic radius increases and the valence electron is farther from the nucleus and more shielded, so it is removed more easily.
Lithium, being the smallest, holds its outer electron most tightly and therefore has the highest first ionization enthalpy of the listed alkali metals.
✓Final answerThe correct option is (E).
- KEAM 2025Set pha-2025-0429F4 marksMCQQ.The correct order of ionization enthalpy is (A) C < B < O < N (B) B < O < C < N (C) N < C < O < B (D) B < C < O < N (E) C < B < O < N
›Reveal solutionSolution
[!TLDR]
Ranking the first ionization enthalpies of B, C, N and O gives the increasing order B<C<O<N, so option (D) is correct.
Concept
In this NCERT/CBSE-aligned periodic-trends topic, ionization enthalpy increases across a period as nuclear charge grows. The one exception among these elements is nitrogen: its stable, exactly half-filled 2s22p3 subshell makes it harder to ionize than oxygen, whose 2p4 configuration has one paired electron that is easier to remove.
Solution
The standard first ionization enthalpies (kJ/mol) are:
B≈801,C≈1086,O≈1314,N≈1402
Arranging from smallest to largest:
801(B)<1086(C)<1314(O)<1402(N)
Hence B<C<O<N. The reversal of O and N is the tell-tale half-filled-stability effect.
[!ANSWER]
(D) B<C<O<N
- KEAM 2025Set pha-2025-0429F4 marksMCQQ.The first and second ionization enthalpies of lanthanoids are comparable with the element (A) Chromium (B) Calcium (C) Germanium (D) Cesium (E) Cadmium
›Reveal solutionSolution
The first and second ionization enthalpies of the lanthanoids are relatively low and lie in the same range as those of calcium, reflecting the ease of forming the common +2/+3 states.
Reasoning
Across the lanthanoid series the first and second ionization enthalpies remain fairly low and change little (poor shielding by 4f electrons keeps them comparable). Their values are of the same order as calcium's, which is why lanthanoids readily attain the +3 (and sometimes +2) oxidation states. This comparison with calcium is a standard NCERT statement.
✓Final answerThe correct option is (B).
- KEAM 2024Set eng-2024-06094 marksMCQQ.The decreasing order of first ionisation enthalpy of the following elements is (A) N>O>C>Be (B) O>N>C>Be (C) Be>C>O>N (D) O>N>Be>Ce (E) N>O>Be>C
›Reveal solutionSolution
Approximate IE1 values: N (1402) > O (1314) > C (1086) > Be (899 kJmol−1), giving N>O>C>Be.
Ionisation enthalpy generally rises across a period, but nitrogen's extra stable half-filled 2p3 configuration makes its IE1 higher than oxygen's (removing an electron from O's paired 2p4 is easier). Carbon (2p2) is lower than both, and beryllium (2s2) lowest of these four:
N(1402)>O(1314)>C(1086)>Be(899) kJmol−1.
Hence the decreasing order is N>O>C>Be.
✓Final answerThe correct option is (A).
- KEAM 2023Set eng-2023-P1-A14 marksMCQQ.The correct of variation of first ionisation enthalpies is: (A) Ne<Xe>Li>K<Cs (B) Xe<Li>K<Cs<Ne (C) Cs>K>Li>Xe<Ne (D) Li>K>Cs>Ne<Xe (E) Ne>Xe>Li>K>Cs
›Reveal solutionSolution
Ionisation enthalpy order is Ne > Xe > Li > K > Cs.
Concept and Intuition
Noble gases have the highest ionisation enthalpies (stable closed shells), and within a group it falls down the column. So the two noble gases lead, with Ne above Xe, followed by the alkali metals Li > K > Cs (decreasing down group 1).
Step-by-Step Solution
- Noble gases first: Ne (approx 2081 kJ/mol) > Xe (approx 1170).
- Alkali metals are far lower and decrease down the group: Li (520) > K (419) > Cs (376).
- Combined order: Ne > Xe > Li > K > Cs.
Common Mistakes
- Placing alkali metals above noble gases, or reversing the down-group trend (thinking Cs > Li).
✓Final answerThe correct option is (E) — Ne > Xe > Li > K > Cs.
ANSWER: E
- KEAM 2021Set eng-2021-P1-A14 marksMCQQ.The first ionisation enthalpy is the least in (A) Germanium (B) Antimony (C) Tellurium (D) Arsenic (E) Bismuth
›Reveal solutionSolution
Bismuth has the lowest first ionisation enthalpy of the options.
Concept and Intuition
First ionisation enthalpy generally increases across a period and decreases down a group as the outer electron gets farther from the nucleus and more shielded. Among the options, bismuth sits lowest in the periodic table.
Step-by-Step Solution
- Approximate IE1 values (kJ mol−1): Ge 762, As 944, Sb 831, Te 869, Bi 703.
- The smallest is bismuth at ≈703.
Common Mistakes
- Assuming a period-3/4 element like Ge is lowest, ignoring the group trend that favours Bi.
✓Final answerThe correct option is (E) — Bismuth.
ANSWER: E
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