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JEE Mains Chemistry · Chemical Bonding and Molecular Structure

Dipole Moment, Hydrogen Bonding and Intermolecular Forces

A molecule's dipole moment is the vector sum of its bond dipoles and lone-pair moments, so symmetry can cancel it; hydrogen bonds and other intermolecular forces then decide how molecules hold together.

Why this matters

Twenty-seven PYQs, nineteen of them multiple choice, and two from 2026. Seven ask about the size or direction of a dipole moment, most often NH₃ against NF₃; nine count or pick polar and non-polar molecules; eleven test hydrogen bonding and other intermolecular forces. Three ideas cover the page.

Concept 1 of 3: Dipole moment: size and direction

When two bonded atoms differ in electronegativity, the shared electrons shift towards one of them, leaving a small positive and a small negative end. The dipole moment is that charge times the distance between the ends. In a molecule, the bond moments and any lone-pair moment add as vectors.

Definition

  • μ=q×d\mu = q \times d. Unit: debye, 1 D=10−181\ \text{D} = 10^{-18} esu cm =3.336×10−30= 3.336 \times 10^{-30} C m. The electron's charge is 4.8×10−104.8 \times 10^{-10} esu.
  • Chemists draw a crossed arrow from the positive end to the negative end: the cross at the positive end, the head at the negative end, showing where the electron density moves.
  • NH3\mathrm{NH_3} (1.47 D) > NF3\mathrm{NF_3} (0.23 D). In NH3\mathrm{NH_3} the N–H bond moments point towards N and add to the lone-pair moment. In NF3\mathrm{NF_3} the N–F bond moments point away from N and partly cancel it.
  • Values to know: H2O\mathrm{H_2O} 1.85, NH3\mathrm{NH_3} 1.47, CHCl3\mathrm{CHCl_3} 1.04, H2S\mathrm{H_2S} 0.95, HBr 0.79, NF3\mathrm{NF_3} 0.23 D.
  • Fraction of ionic character =μobservedμfully ionic= \dfrac{\mu_{\text{observed}}}{\mu_{\text{fully ionic}}}, with μfully ionic=e×d\mu_{\text{fully ionic}} = e \times d.

Dipole moment

μ=q×d1 D=10−18 esu cm\mu = q \times d \qquad 1\ \text{D} = 10^{-18}\ \text{esu cm}

Worked example

HCl has a dipole moment of 1.07 D and a bond length of 1.27 Å. Find the partial charge on each atom in esu, and the fraction of an electron's charge it represents (e=4.8×10−10e = 4.8 \times 10^{-10} esu).
Practice this conceptself-check · 4 quick reps

The same idea in a real exam question:

JEE Mains · 2026 · 22 Jan 2026 Shift 2 · Q36Moderate

Example 1 · Chemical Bonding and Molecular Structure · Dipole Moment, Hydrogen Bonding and Intermolecular Forces

Among H2 S,H2O,NF3,NH3H_{2}\text{ }S,H_{2}O,NF_{3},NH_{3} and CHCl3CHCl_{3}, identify the molecule (X)(X) with lowest dipole moment value. The number of lone pairs of electrons present on the central atom of the molecule (X)(X) is :

More electronegative F does not mean a bigger dipole

Each N–F bond is more polar than an N–H bond, yet NF3\mathrm{NF_3} (0.23 D) is far less polar than NH3\mathrm{NH_3} (1.47 D). The lone-pair moment adds to the bond moments in NH3\mathrm{NH_3} and opposes them in NF3\mathrm{NF_3}.

The two arrow conventions point opposite ways

The chemist's arrow runs from positive to negative, following the electron density. The physicist's dipole vector runs from negative to positive. A statement that puts the tail on the negative centre describes the physics convention.

Concept 2 of 3: Polar or non-polar: when symmetry cancels

Polar bonds do not always make a polar molecule. If identical bonds point symmetrically around the centre with no lone pair to spoil the balance, their moments cancel to zero. Change one outer atom, or add a lone pair that bends the shape, and a net dipole appears.

Definition

  • Zero dipole: symmetric shapes with identical outer atoms and no net lone-pair moment: linear AX₂, trigonal planar AX₃, tetrahedral AX₄, square planar AX₄E₂, trigonal bipyramidal AX₅, octahedral AX₆, and linear AX₂E₃.
  • Non-zero dipole: bent, pyramidal, see-saw, T-shaped and square pyramidal shapes; any heteronuclear diatomic; a symmetric shape with mixed outer atoms (CHCl3\mathrm{CHCl_3}, CH2Cl2\mathrm{CH_2Cl_2}).
  • Organic: pp-dichlorobenzene and trans-1,2-dichloroethene have zero dipole; the ortho and meta isomers and the cis isomer are polar.
  • A homonuclear diatomic (H2\mathrm{H_2}, N2\mathrm{N_2}) is non-polar.
ShapeNet dipoleExamples
Linear AX₂ or AX₂E₃ZeroCO2\mathrm{CO_2}, BeF2\mathrm{BeF_2}, BeCl2\mathrm{BeCl_2}, XeF2\mathrm{XeF_2}
Trigonal planar AX₃ZeroBF3\mathrm{BF_3}, BCl3\mathrm{BCl_3}, SO3\mathrm{SO_3}
Tetrahedral AX₄ZeroCH4\mathrm{CH_4}, CCl4\mathrm{CCl_4}, SiF4\mathrm{SiF_4}
Square planar, TBP, octahedralZeroXeF4\mathrm{XeF_4}, PCl5\mathrm{PCl_5}, SF6\mathrm{SF_6}
BentNon-zeroH2O\mathrm{H_2O}, H2S\mathrm{H_2S}, SO2\mathrm{SO_2}
PyramidalNon-zeroNH3\mathrm{NH_3}, NF3\mathrm{NF_3}, PCl3\mathrm{PCl_3}
See-saw, T-shaped, square pyramidalNon-zeroSF4\mathrm{SF_4}, ClF3\mathrm{ClF_3}, BrF5\mathrm{BrF_5}
Tetrahedral with mixed atomsNon-zeroCHCl3\mathrm{CHCl_3}, CH2Cl2\mathrm{CH_2Cl_2}
Heteronuclear diatomicNon-zeroHF, HCl, HBr
H₂ has zero dipole; HF, with the biggest electronegativity gap, has the largest of the hydrogen halides.
A lone pair on the centre breaks the symmetry unless the lone pairs themselves are placed symmetrically, as in XeF₂ and XeF₄.
Practice this conceptself-check · 4 quick reps

The same idea in a real exam question:

JEE Mains · 2024 · 5 Apr 2024 · Q150Moderate

Example 2 · Chemical Bonding and Molecular Structure · Dipole Moment, Hydrogen Bonding and Intermolecular Forces

Number of compounds from the following with zero dipole moment is ____ . HF,H2,H2 S,CO2,NH3,BF3,CH4,CHCl3,SiF4HF,H_{2},H_{2}\text{ }S,CO_{2},NH_{3},BF_{3},CH_{4},CHCl_{3},SiF_{4}, H2O,BeF2H_{2}O,BeF_{2}

Polar bonds can give a non-polar molecule

C–Cl and B–F bonds are strongly polar, but CCl4\mathrm{CCl_4} and BF3\mathrm{BF_3} have zero dipole moment. Ask whether the shape is symmetric, not whether the bonds are polar.

Lone pairs do not always make a molecule polar

XeF4\mathrm{XeF_4} has two lone pairs and XeF2\mathrm{XeF_2} has three, yet both are non-polar: the lone pairs sit opposite each other or round the equator, and their moments cancel.

Concept 3 of 3: Hydrogen bonding and intermolecular forces

A hydrogen bonded to F, O or N is left almost bare, so it is pulled strongly towards a lone pair on a nearby F, O or N. That is a hydrogen bond. It can link two molecules (intermolecular) or two groups inside one molecule (intramolecular), and which one happens changes boiling points and volatility.

Definition

  • A hydrogen bond needs H covalently bonded to a small, highly electronegative atom (F, O, N) and a lone pair on another such atom.
  • Intermolecular H-bonds join molecules: water, HF (zig-zag chains), NH3\mathrm{NH_3}, pp-nitrophenol. They raise the boiling point.
  • Intramolecular H-bonds close a ring inside one molecule: oo-nitrophenol, salicylaldehyde. The molecule has fewer links to its neighbours, so it boils lower and is steam volatile.
  • The extent of H-bonding depends on the physical state: ice > liquid water > vapour; dissolved impurities disrupt it.
  • Other forces: London (dispersion) forces act between all molecules, with energy ∝1/r6\propto 1/r^6; dipole-dipole energy ∝1/r3\propto 1/r^3 for fixed polar molecules and 1/r61/r^6 for rotating ones.
CaseKind of attractionEffect
HFIntermolecular H-bonds, zig-zag chainsThe strongest single H-bond; the H sits nearer one F, so the bonds are not symmetrical
Ice, water, water with soluteIntermolecular H-bondsMost in ice (each molecule bonded four ways), fewer in liquid water, fewer again with impurities
oo-Nitrophenol, salicylaldehydeIntramolecular H-bondLower boiling point; steam volatile
pp-Nitrophenol, pp-hydroxybenzaldehydeIntermolecular H-bondsHigher boiling point; not steam volatile
CH4<HCN<NH3\mathrm{CH_4 < HCN < NH_3}None, weak C–H···N, N–H···NOrder of intermolecular H-bond strength
Noble gases, CH4\mathrm{CH_4}London forces onlyEnergy ∝1/r6\propto 1/r^6; grows with molecular size
Ar, CH4\mathrm{CH_4}, H2O\mathrm{H_2O}, C6H6\mathrm{C_6H_6}Van der Waals constant a (about 1.4, 2.3, 5.5, 18 L² bar mol⁻²)Larger a means stronger attraction between molecules
H bonded to F, O or N gives a hydrogen bond; where it forms, inside or between molecules, decides the boiling point.
Practice this conceptself-check · 4 quick reps

The same idea in a real exam question:

JEE Mains · 2024 · 4 April 2024 · Q124Moderate

Example 3 · Chemical Bonding and Molecular Structure · Dipole Moment, Hydrogen Bonding and Intermolecular Forces

The correct statement/s about Hydrogen bonding is/are: (A) Hydrogen bonding exists when HH is covalently bonded to the highly electro negative atom. (B) Intermolecular HH bonding is present in o-nitro phenol (C) Intramolecular HH bonding is present in HFHF. (D) The magnitude of HH bonding depends on the physical state of the compound. (E) H-bonding has powerful effect on the structure and properties of compounds. Choose the correct answer from the options given below:

Ortho means intramolecular

The ortho isomer of a nitrophenol or hydroxybenzaldehyde bonds within itself; the para isomer bonds to its neighbours. Swapping them reverses every boiling-point and volatility answer.

HF has no intramolecular hydrogen bond

One HF molecule has a single H–F bond, so it cannot bond to itself. Its hydrogen bonds link separate molecules into chains, and they are not symmetrical.

Summary — formulas & gotchas at a glance

A revision cheat-sheet for the formulas and gotchas above. Click any concept name to jump back to its full explanation.

Formulas (1)

Reference tables (2)

Polar or non-polar: when symmetry cancels9 rows
ShapeNet dipoleExamples
Linear AX₂ or AX₂E₃ZeroCO2\mathrm{CO_2}, BeF2\mathrm{BeF_2}, BeCl2\mathrm{BeCl_2}, XeF2\mathrm{XeF_2}
Trigonal planar AX₃ZeroBF3\mathrm{BF_3}, BCl3\mathrm{BCl_3}, SO3\mathrm{SO_3}
Tetrahedral AX₄ZeroCH4\mathrm{CH_4}, CCl4\mathrm{CCl_4}, SiF4\mathrm{SiF_4}
Square planar, TBP, octahedralZeroXeF4\mathrm{XeF_4}, PCl5\mathrm{PCl_5}, SF6\mathrm{SF_6}
BentNon-zeroH2O\mathrm{H_2O}, H2S\mathrm{H_2S}, SO2\mathrm{SO_2}
PyramidalNon-zeroNH3\mathrm{NH_3}, NF3\mathrm{NF_3}, PCl3\mathrm{PCl_3}
See-saw, T-shaped, square pyramidalNon-zeroSF4\mathrm{SF_4}, ClF3\mathrm{ClF_3}, BrF5\mathrm{BrF_5}
Tetrahedral with mixed atomsNon-zeroCHCl3\mathrm{CHCl_3}, CH2Cl2\mathrm{CH_2Cl_2}
Heteronuclear diatomicNon-zeroHF, HCl, HBr
H₂ has zero dipole; HF, with the biggest electronegativity gap, has the largest of the hydrogen halides.
A lone pair on the centre breaks the symmetry unless the lone pairs themselves are placed symmetrically, as in XeF₂ and XeF₄.
Hydrogen bonding and intermolecular forces7 rows
CaseKind of attractionEffect
HFIntermolecular H-bonds, zig-zag chainsThe strongest single H-bond; the H sits nearer one F, so the bonds are not symmetrical
Ice, water, water with soluteIntermolecular H-bondsMost in ice (each molecule bonded four ways), fewer in liquid water, fewer again with impurities
oo-Nitrophenol, salicylaldehydeIntramolecular H-bondLower boiling point; steam volatile
pp-Nitrophenol, pp-hydroxybenzaldehydeIntermolecular H-bondsHigher boiling point; not steam volatile
CH4<HCN<NH3\mathrm{CH_4 < HCN < NH_3}None, weak C–H···N, N–H···NOrder of intermolecular H-bond strength
Noble gases, CH4\mathrm{CH_4}London forces onlyEnergy ∝1/r6\propto 1/r^6; grows with molecular size
Ar, CH4\mathrm{CH_4}, H2O\mathrm{H_2O}, C6H6\mathrm{C_6H_6}Van der Waals constant a (about 1.4, 2.3, 5.5, 18 L² bar mol⁻²)Larger a means stronger attraction between molecules
H bonded to F, O or N gives a hydrogen bond; where it forms, inside or between molecules, decides the boiling point.

Watch out for (6)

Test yourself on Chemical Bonding and Molecular Structure

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