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Periodic Classification of Elements: Complete CBSE Class 10 Notes

By Shailendra Singh

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Updated on 11 Nov 2025, 18:21 IST

Introduction to Periodic Classification

The periodic classification of elements is one of the most fundamental organizing principles in chemistry. Before the 18th century, when only about 30 elements were known, studying and remembering their properties was relatively simple. However, as more elements were discovered, the need arose for a systematic method to organize them based on their properties.

The periodic table arranges all known elements according to their properties in such a way that elements with similar properties are grouped together in a tabular form. This arrangement has evolved through several stages, from early attempts like Dobereiner's triads and Newlands' law of octaves to Mendeleev's periodic table, and finally to the modern periodic table we use today.

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Historical Development of Periodic Classification

Dobereiner's Triads (1817)

German chemist Johann Wolfgang Dobereiner arranged elements in groups of three (triads) where the atomic mass of the middle element was roughly the average of the other two elements.

Example:

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  • Lithium (7), Sodium (23), Potassium (39)
  • Average of Li and K: (7 + 39)/2 = 23 (Na's atomic mass)

Limitations:

  • Could only classify a limited number of elements
  • Only three triads could be identified at that time

Newlands' Law of Octaves (1866)

J.A.R. Newlands arranged elements in order of increasing atomic mass and observed that every eighth element had properties similar to the first, like musical octaves.

Periodic Classification of Elements: Complete CBSE Class 10 Notes

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Limitations:

  1. Applicable only up to calcium
  2. Worked well only with lighter elements
  3. Could not accommodate newly discovered elements
  4. Placed dissimilar elements together (Co, Ni with F, Cl, Br)
  5. Placed similar elements far apart (Fe away from Co and Ni)

Mendeleev's Periodic Table (1869)

Dmitri Ivanovich Mendeleev arranged 63 known elements in increasing order of atomic mass and grouped them based on chemical properties.

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Achievements:

  1. Systematic study - Made studying elements easier
  2. Prediction of new elements - Left gaps for undiscovered elements (Scandium, Gallium, Germanium)
  3. Correction of atomic masses - Corrected values for Be, In, U, and Pt
  4. Accommodation of noble gases - New group added without disturbing existing order

Drawbacks:

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  1. Uncertain position of hydrogen - Similar to both alkali metals and halogens
  2. Isotopes problem - No separate positions for isotopes
  3. Anomalous pairs - Ar before K, Co before Ni, Te before I
  4. Similar elements separated - Ag and Tl, Ba and Pb placed in different groups
  5. Dissimilar elements together - Cu and Hg in same group despite differences
  6. No explanation of periodicity
  7. No clear separation of metals and non-metals

Modern Periodic Law

The Law

In 1913, Henry Moseley discovered that properties of elements depend on their atomic number rather than atomic mass. This led to the Modern Periodic Law:

"The physical and chemical properties of elements are periodic functions of their atomic numbers."

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Significance of Modern Periodic Law

  1. Eliminates atomic mass anomalies - Resolves issues like Ar-K, Co-Ni placement
  2. Provides proper position for isotopes - All isotopes have same atomic number, so occupy same position
  3. Based on electronic configuration - Properties depend on number of electrons, not mass
  4. Explains periodicity - Similar valence electron configurations lead to similar properties
  5. More fundamental basis - Atomic number is a more fundamental property than atomic mass

The modern periodic law recognizes that chemical properties depend on the number of valence electrons, which in turn depends on atomic number. When elements are arranged in increasing order of atomic numbers, elements with the same number of valence electrons appear at regular intervals, creating periodicity.

Structure of Modern Periodic Table

The modern periodic table, also called the long form or Bohr, Bury & Rang, Werner periodic table, consists of:

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  • 18 vertical columns (Groups) - Elements with same number of valence electrons
  • 7 horizontal rows (Periods) - Elements with same number of shells

Periods

PeriodPrincipal Quantum Number (n)Subshells FilledNumber of ElementsRangeName
111s2H to HeShortest
222s, 2p8Li to NeShort
333s, 3p8Na to ArShort
444s, 3d, 4p18K to KrLong
555s, 4d, 5p18Rb to XeLong
666s, 4f, 5d, 6p32Cs to RnLongest
777s, 5f, 6d26 (incomplete)Fr to UubIncomplete

Period = Number of shells in the atom

Groups

Groups are numbered from 1 to 18 according to IUPAC recommendations.

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Key Groups:

  • Group 1 (IA) - Alkali metals
  • Group 2 (IIA) - Alkaline earth metals
  • Group 13 (IIIA) - Boron family
  • Group 14 (IVA) - Carbon family
  • Group 15 (VA) - Nitrogen family/Pnictogens
  • Group 16 (VIA) - Oxygen family/Chalcogens
  • Group 17 (VIIA) - Halogens (salt-forming)
  • Group 18 (0/VIIIA) - Noble gases/Inert gases

Group Number = Number of valence electrons (for main group elements)

Classification Based on Electronic Configuration: s, p, d, f Blocks

Elements are classified into four blocks based on which subshell receives the last electron:

s-Block Elements

Electronic Configuration: ns¹⁻²

Characteristics:

  • Groups 1 and 2
  • Highly electropositive (metallic)
  • Low ionization energies
  • Form cations easily
  • Good reducing agents
  • Examples: Li, Na, K (Group 1); Be, Mg, Ca (Group 2)

General Configuration:

  • Group 1: [Noble gas] ns¹
  • Group 2: [Noble gas] ns²

p-Block Elements

Electronic Configuration: ns² np¹⁻⁶

Characteristics:

  • Groups 13 to 18
  • Include metals, non-metals, and metalloids
  • Properties vary from metallic to non-metallic across the period
  • Form both cations and anions
  • Examples: B, Al (Group 13); C, Si (Group 14); N, P (Group 15); O, S (Group 16); F, Cl (Group 17); He, Ne (Group 18)

Valence Electrons: Number of electrons in outermost s and p subshells

Group Number = 10 + number of valence electrons

Characteristics:

  • Groups 3 to 12
  • All are metals
  • Form colored ions and compounds
  • Show variable oxidation states
  • Good catalysts
  • Form complex compounds
  • High melting and boiling points
  • Examples: Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn

Group Number = Number of electrons in (n-1)d + number in ns

Note: Zn, Cd, Hg with d¹⁰ configuration are sometimes not considered true transition elements because d subshell is completely filled.

f-Block Elements (Inner Transition Elements)

Electronic Configuration: (n-2)f¹⁻¹⁴ (n-1)d⁰⁻¹ ns²

Characteristics:

  • Placed separately at bottom of periodic table
  • Two series:
    • Lanthanides (4f series): Ce (58) to Lu (71)
    • Actinides (5f series): Th (90) to Lr (103)
  • All are metals
  • Show similar properties within each series
  • Most actinides are synthetic (artificial)
  • Radioactive elements

Properties:

  • Similar chemical behavior within series
  • Difficulty in separation
  • Form colored ions
  • Show magnetic properties

Comparison: Mendeleev's vs Modern Periodic Table

AspectMendeleev's Periodic TableModern Periodic Table
Basis of ClassificationIncreasing atomic massIncreasing atomic number
Periodic LawProperties are periodic function of atomic massProperties are periodic function of atomic number
Number of Groups8 groups (divided into A and B subgroups)18 groups
Number of Periods6 periods7 periods
Position of ElementsBased on atomic mass and propertiesBased on electronic configuration
IsotopesNo proper position (should be placed separately)Same position (same atomic number)
HydrogenUncertain positionPlaced above alkali metals
Noble GasesNot present initially (added later)Group 18 (0 group)
Anomalous PairsPresent (Ar-K, Co-Ni, Te-I)Resolved by atomic number arrangement
Transition ElementsPlaced in group VIII outside main tableSeparate d-block (Groups 3-12)
Metals and Non-metalsNo clear distinctionClearly separated
Explanation of PeriodicityNot explainedExplained by electronic configuration
PredictionsLeft gaps for undiscovered elementsNo gaps (except in period 7)

Periodic properties are characteristics that show regular variations when moving across a period or down a group.

1. Atomic Size (Atomic Radius)

Definition: Distance from the center of nucleus to the outermost shell containing electrons.

Types:

  • Covalent Radius: Half the distance between nuclei of two bonded identical atoms
  • Metallic Radius: Half the inter-nuclear distance between two adjacent metal atoms
  • Van der Waals Radius: Half the distance between nuclei of two adjacent non-bonded atoms (= 2 × Covalent Radius)

Trends:

Across a Period (Left to Right):

  • Decreases
  • Reason: Nuclear charge increases while electrons are added to same shell
  • Effective nuclear charge increases, pulling electrons closer
  • Example: Li (152 pm) > Be (111 pm) > B (88 pm) > C (77 pm) > N (74 pm) > O (66 pm) > F (64 pm)

Down a Group (Top to Bottom):

  • Increases
  • Reason: New shells are added
  • Distance from nucleus increases
  • Shielding effect increases
  • Example: Li (152 pm) < Na (186 pm) < K (231 pm) < Rb (244 pm) < Cs (262 pm)

2. Ionic Radius

Cationic Radius:

  • Cation is smaller than parent atom
  • Reason: Loss of electron(s) reduces electron-electron repulsion
  • Size decreases as positive charge increases
  • Example: Fe > Fe²⁺ > Fe³⁺

Anionic Radius:

  • Anion is larger than parent atom
  • Reason: Gain of electron(s) increases electron-electron repulsion
  • Effective nuclear charge per electron decreases
  • Example: Cl < Cl⁻

Isoelectronic Species:

  • Species with same number of electrons
  • Size decreases with increasing nuclear charge
  • Example: O²⁻ (1.40 Å) > F⁻ (1.36 Å) > Na⁺ (0.95 Å) > Mg²⁺ (0.65 Å) > Al³⁺ (0.50 Å)

3. Ionization Energy (Ionization Potential)

Definition: Minimum energy required to remove the most loosely bound electron from an isolated gaseous neutral atom.

Equation: M(g) + Energy → M⁺(g) + e⁻

Units: kJ/mol or eV

Successive Ionization Energies:

  • First IE (IE₁): M(g) → M⁺(g) + e⁻
  • Second IE (IE₂): M⁺(g) → M²⁺(g) + e⁻
  • Always: IE₁ < IE₂ < IE₃...

Trends:

Across a Period:

  • Generally increases (left to right)
  • Reason: Atomic size decreases, nuclear charge increases
  • Exceptions: Be > B, N > O (due to stable configurations)
  • Example: Li < Be > B < C < N > O < F < Ne

Down a Group:

  • Decreases
  • Reason: Atomic size increases, shielding effect increases
  • Outermost electrons are farther from nucleus
  • Example: Li > Na > K > Rb > Cs

Factors Affecting IE:

  1. Atomic size (IE ∝ 1/size)
  2. Nuclear charge (IE ∝ Z)
  3. Shielding effect (IE ∝ 1/shielding)
  4. Electronic configuration (stable configs have higher IE)

4. Electron Affinity (Electron Gain Enthalpy)

Definition: Energy released when an isolated gaseous atom accepts an electron to form a negative ion.

Equation: X(g) + e⁻ → X⁻(g) + Energy

Units: kJ/mol (usually reported as negative values)

Trends:

Across a Period:

  • Generally increases (becomes more negative)
  • Reason: Atomic size decreases, nuclear charge increases
  • Attraction for additional electron increases
  • Example: C < N < O < F < Ne (nearly zero)

Down a Group:

  • Generally decreases (becomes less negative)
  • Reason: Atomic size increases
  • Additional electron enters farther shell
  • Exception: Cl > F (due to small size and electron-electron repulsion in F)

Special Cases:

  • Noble gases: Nearly zero (stable configuration)
  • Nitrogen: Lower than expected (half-filled p³ stability)
  • Second electron affinity: Always endothermic (positive)
    • O⁻(g) + e⁻ → O²⁻(g) (requires energy)

5. Electronegativity

Definition: Tendency of an atom to attract shared pair of electrons towards itself in a covalent bond.

Scales:

  • Pauling Scale (most common)
  • Mulliken Scale: Based on IE and EA
    • χ = (IE + EA)/2

Trends:

Across a Period:

  • Increases (left to right)
  • Reason: Atomic size decreases, ability to attract electrons increases
  • Example: Li (1.0) < Be (1.5) < B (2.0) < C (2.5) < N (3.0) < O (3.5) < F (4.0)

Down a Group:

  • Decreases
  • Reason: Atomic size increases, attraction for bonding electrons decreases
  • Example: F (4.0) > Cl (3.0) > Br (2.8) > I (2.5)

Most Electronegative: Fluorine (4.0) Least Electronegative: Francium/Cesium (~0.7)

6. Metallic and Non-metallic Character

Metallic Character: Tendency to lose electrons and form positive ions.

Trends:

  • Decreases across a period (left to right)
  • Increases down a group
  • Most metallic: Francium/Cesium (bottom-left)
  • Least metallic: Fluorine (top-right)

Non-metallic Character: Tendency to gain electrons and form negative ions.

Trends:

  • Increases across a period
  • Decreases down a group
  • Most non-metallic: Fluorine

7. Valency

Definition: Combining capacity of an element.

Trends:

Across a Period:

  • With respect to H and halogens: 1 → 4 → 1
  • With respect to O: 1 → 7
  • Example (Period 3): Na(1), Mg(2), Al(3), Si(4), P(3), S(2), Cl(1), Ar(0)

Down a Group:

  • Remains constant (same number of valence electrons)
  • Example (Group 1): All have valency = 1
PropertyAcross Period (→)Down Group (↓)
Atomic SizeDecreasesIncreases
Ionization EnergyIncreasesDecreases
Electron AffinityIncreases (more negative)Decreases (less negative)
ElectronegativityIncreasesDecreases
Metallic CharacterDecreasesIncreases
Non-metallic CharacterIncreasesDecreases
Valency1→4→1 (with H), 1→7 (with O)Constant
Chemical Reactivity (Metals)DecreasesIncreases
Chemical Reactivity (Non-metals)IncreasesDecreases

Common Exceptions to Predicted Electronic Configurations

1. Chromium (Z = 24)

Expected: [Ar] 3d⁴ 4s² Actual: [Ar] 3d⁵ 4s¹

Reason: Half-filled d subshell (d⁵) is more stable than d⁴

2. Copper (Z = 29)

Expected: [Ar] 3d⁹ 4s² Actual: [Ar] 3d¹⁰ 4s¹

Reason: Fully-filled d subshell (d¹⁰) is more stable than d⁹

3. Palladium (Z = 46)

Expected: [Kr] 4d⁸ 5s² Actual: [Kr] 4d¹⁰ 5s⁰

Reason: Completely filled d¹⁰ configuration is exceptionally stable

Why These Exceptions Occur

  1. Extra stability of half-filled and fully-filled subshells
    • Exchange energy is maximized
    • Symmetrical distribution of electrons
    • Lower electron-electron repulsion
  2. Energy difference between (n-1)d and ns orbitals is small
    • Easy to promote one s electron to d orbital
    • Resulting configuration has lower overall energy
  3. Pattern:
    • d⁵s¹ is more stable than d⁴s²
    • d¹⁰s¹ is more stable than d⁹s²

Formulas and Relationships

PropertyFormula/RelationshipExplanation
Mendeleev's TriadAtomic mass of middle element = (First + Third)/2Average of first and third element equals middle element
Modern Periodic LawProperties = f(Atomic Number)Properties are periodic function of atomic number
Group Number (p-block)Group Number = 10 + valence electronsFor elements in p-block
Group Number (d-block)Group Number = (n-1)d electrons + ns electronsFor transition elements
Period NumberPeriod = Number of shells (n)Highest principal quantum number
Van der Waals Radiusr(VdW) = 2 × r(covalent)Relationship between radii types
Atomic Size TrendSize ∝ 1/ZeffInversely proportional to effective nuclear charge
Ionization EnergyM(g) → M⁺(g) + e⁻ ; ΔH = IEEnergy required to remove electron
Successive IEIE₁ < IE₂ < IE₃ ...Each successive ionization requires more energy
Electron AffinityX(g) + e⁻ → X⁻(g) + EnergyEnergy released when electron is added
Mulliken Electronegativityχ = (IE + EA)/2Average of ionization energy and electron affinity
Ionic vs Atomic Radiusr(cation) < r(atom) < r(anion)Relative size relationship
Isoelectronic SeriesSize ∝ 1/ZInversely proportional to nuclear charge
Effective Nuclear ChargeZeff = Z - SNuclear charge minus shielding

Important Points to Remember

About Blocks

  1. s-block: Only groups 1 and 2
  2. p-block: Groups 13-18; includes most non-metals
  3. d-block: Groups 3-12; all transition metals
  4. f-block: Lanthanides (4f) and Actinides (5f)

About Periodicity

  1. Periodicity occurs because of repeating valence shell electronic configurations
  2. Similar properties arise from same number of valence electrons
  3. Position determines properties: Group determines valency, period determines size

About Atomic Size

  1. Smallest atom: Hydrogen (in period 1) or Helium (overall)
  2. Largest atom: Francium or Cesium
  3. In period 3: Na (largest) to Ar (smallest)

About Ionization Energy

  1. Highest IE: Helium/Neon (noble gases)
  2. Lowest IE: Francium/Cesium (alkali metals)
  3. IE₁ < IE₂ < IE₃ always

About Electron Affinity

  1. Highest EA: Chlorine (not fluorine due to size)
  2. Lowest EA: Noble gases (nearly zero)
  3. Second EA is always endothermic (positive)

About Electronegativity

  1. Most electronegative: Fluorine (4.0)
  2. Least electronegative: Cesium/Francium (~0.7)
  3. Trend: Increases diagonally towards fluorine

Practice Questions

Conceptual Questions

  1. Why do elements in the same group have similar properties?
  2. How did Moseley's work improve upon Mendeleev's periodic table?
  3. Explain why the second ionization energy is always greater than the first.
  4. Why is the electron affinity of chlorine greater than fluorine?
  5. What makes half-filled and fully-filled subshells particularly stable?

Application Questions

  1. Predict the electronic configuration of element with atomic number 26.
  2. Arrange the following in order of increasing atomic size: N, O, F, P, S
  3. Which element has higher ionization energy: Na or Mg? Why?
  4. Predict the valency of an element in group 15.
  5. Identify the block and group of an element with configuration [Ar] 3d⁵ 4s²

Preparations Tips

  1. Understand trends, don't just memorize - Know the reasons behind periodic trends
  2. Practice electronic configurations - Especially for d-block elements and exceptions
  3. Remember IUPAC group numbering - 1-18, not the old IA-VIIIA system
  4. Focus on exceptions - Cr, Cu, Pd configurations are frequently asked
  5. Compare Mendeleev and Modern tables - Basis, advantages, limitations
  6. Know specific examples - For each trend, remember 2-3 examples
  7. Understand isoelectronic series - Size trend is often tested
  8. Differentiate between concepts - IE vs EA, atomic vs ionic radius

Conclusion

The periodic classification of elements represents one of chemistry's greatest organizational achievements. The journey from Dobereiner's simple triads to the sophisticated modern periodic table demonstrates the evolution of scientific understanding.

The modern periodic law, based on atomic number rather than atomic mass, provides a rational basis for understanding the systematic variation of properties. The division into s, p, d, and f blocks based on electronic configuration offers deep insights into chemical behavior.

Understanding periodic trends how atomic size, ionization energy, electron affinity, and electronegativity vary enables prediction of element properties and reactivity. These trends are not arbitrary but arise logically from electronic structure and effective nuclear charge.

Mastery of the periodic table is essential for all further study in chemistry, as it serves as the fundamental framework for understanding chemical behavior, bonding, and reactions.

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Frequently Asked Questions: Periodic Classification of Elements

What is the periodic table and why was it developed?

The periodic table is a systematic arrangement of all known elements according to their properties, where elements with similar characteristics are grouped together in a tabular format. It was developed because as the number of discovered elements increased beyond 30 in the eighteenth century, scientists needed a simpler method to study and remember their properties. This classification system groups similar elements together while separating different ones, making it easier to predict element behavior and understand chemical relationships.

Who created the modern periodic table and what was it based on?

Dmitri Ivanovich Mendeleev created the most influential periodic table in 1869, arranging 63 known elements by increasing atomic mass and chemical property similarities. However, the modern periodic table is based on the work of Henry Moseley (1913), who demonstrated that atomic number not atomic mass is the fundamental property determining element characteristics. This led to the modern periodic law: "The physical and chemical properties of elements are periodic functions of their atomic numbers."

What were Dobereiner's Triads and what were their limitations?

Dobereiner's Triads (1817) grouped elements in sets of three where the atomic mass of the middle element was roughly the average of the other two. For example, lithium (7), sodium (23), and potassium (39) form a triad where (7+39)/2 = 23. The limitation was that this classification only worked for a small number of elements only a few triads could be identified at the time, making it insufficient for organizing all known elements.

What was Newlands' Law of Octaves and why did it fail?

Newlands' Law of Octaves (1866) stated that when elements are arranged by increasing atomic mass, every eighth element has properties similar to the first, like musical octaves. This pattern worked well only up to calcium and with lighter elements. It failed because it couldn't accommodate elements discovered later, placed dissimilar elements together (like cobalt and nickel with halogens), and separated similar elements (like iron from cobalt and nickel).

How is the modern periodic table organized?

The modern periodic table contains 18 vertical columns called groups and 7 horizontal rows called periods. Elements are arranged by increasing atomic number, with those having the same number of valence electrons placed in the same group. The table includes 118 confirmed elements and distinguishes between s-block, p-block, d-block (transition elements), and f-block (lanthanides and actinides) elements based on which subshell receives the last electron.

What are periods and how many elements does each contain?

Periods are horizontal rows in the periodic table. Period 1 is the shortest with 2 elements (H, He). Periods 2 and 3 are short periods with 8 elements each. Periods 4 and 5 are long periods with 18 elements each. Period 6 is the longest with 32 elements (including lanthanides). Period 7 is incomplete with 26 elements discovered so far (including actinides). The number of elements in each period corresponds to the number of electrons that can occupy the subshells being filled.

What are groups and how are they numbered?

Groups are vertical columns containing elements with similar properties because they have the same number of valence electrons. According to IUPAC recommendations, there are 18 groups numbered 1-18. Group 1 contains alkali metals, Group 2 has alkaline earth metals, Groups 3-12 are transition elements, Groups 13-17 contain representative elements, and Group 18 consists of noble gases. Elements in the same group typically show similar chemical behavior.

What are s-block, p-block, d-block, and f-block elements?

These classifications indicate which atomic subshell receives the last electron. S-block elements (Groups 1-2) have their outermost electron in an s orbital with general configuration ns¹⁻². P-block elements (Groups 13-18) fill p orbitals with configuration ns²np¹⁻⁶. D-block elements (Groups 3-12, transition metals) have configuration (n-1)d¹⁻¹⁰ns⁰⁻². F-block elements (lanthanides and actinides) have configuration (n-2)f¹⁻¹⁴(n-1)d⁰⁻¹ns². This classification helps predict chemical properties and reactivity patterns.

What is effective nuclear charge and how does it affect properties?

Effective nuclear charge (Z_eff) is the net positive charge experienced by valence electrons after accounting for shielding by inner electrons. As you move across a period, Z_eff increases because protons are added but electrons enter the same shell with similar shielding. Down a group, Z_eff remains relatively constant as both nuclear charge and shielding increase proportionally. Higher Z_eff causes smaller atomic size, higher ionization energy, and greater electronegativity explaining most periodic trends.

What causes the lanthanide contraction?

Lanthanide contraction refers to the greater-than-expected decrease in atomic and ionic radii of lanthanide elements (atomic numbers 58-71) and subsequent elements. It occurs because 4f electrons shield outer electrons imperfectly from the increasing nuclear charge. As 4f orbitals fill across the series, each additional proton pulls the entire electron cloud closer, causing size to decrease more than expected. This affects properties of elements following the lanthanides, making 5d transition elements similar in size to 4d elements.

Oxide character changes from basic to acidic as you move from left to right across a period. Metals on the left form basic oxides (like Na₂O, MgO) that react with acids. Metalloids in the middle form amphoteric oxides (like Al₂O₃) that react with both acids and bases. Non-metals on the right form acidic oxides (like SO₂, P₂O₅, Cl₂O₇) that react with bases. This trend reflects the gradual change from metallic to non-metallic character across the period.

What are alkali metals and what are their properties?

Alkali metals (Group 1: Li, Na, K, Rb, Cs, Fr) have one electron in their outermost shell (ns¹ configuration), making them highly reactive metals with low ionization energies. They readily lose this electron to form +1 ions. Metallic character and reactivity increase down the group, with cesium being the most metallic and reactive (excluding radioactive francium). They all react with water to produce hydrogen gas and form strongly basic hydroxides.

What are transition elements and what makes them special?

Transition elements (d-block, Groups 3-12) have their last electron entering (n-1)d orbitals with general configuration (n-1)d¹⁻¹⁰ns⁰⁻². They show variable valency because both ns and (n-1)d electrons can participate in bonding. These elements typically form colored compounds, exhibit catalytic properties, and can form complex ions. They show less dramatic property changes across a period compared to representative elements due to similar outer shell configurations.

What is atomic size and how does it vary in the periodic table?

Atomic size (atomic radius) is the distance from the nucleus to the outermost electrons. In a group, atomic size increases from top to bottom as new electron shells are added, increasing the distance from the nucleus. Across a period from left to right, atomic size decreases because the nuclear charge increases while electrons are added to the same shell, pulling electrons closer. For example, in Period 2, lithium is the largest atom and fluorine is the smallest.