JEE Main 2025 · 22 January · evening · Single correct · +4 / −1
Arrange the following compounds in increasing order of their dipole moment :
HBr, H₂ S, NF₃ and CHCl₃
- (a) HBr<H₂ S<NF₃<CHCl₃
- (b) H₂ S<HBr<NF₃<CHCl₃
- (c) NF₃<HBr<H₂ S<CHCl₃
- (d) CHCl₃<NF₃<HBr<H₂ S
Answer and solution
Answer (c) NF₃<HBr<H₂ S<CHCl₃
Solution
Chemistry ma’am · 4 steps
NF₃ is the surprise here: its lone pair works against the N–F bonds, so it comes last.
- NF3 nearly cancels. In NF₃ each N–F bond moment points away from N, towards the very electronegative F. The lone pair on N points the other way, so the two effects largely cancel and μ is only about 0.23 D.
- HBr versus H2S. HBr has one polar bond, with an electronegativity difference of about 0.8. H₂S has weaker S–H bonds, but it is bent, so its two bond moments and its lone pairs add up. That puts H₂S slightly above HBr.
- CHCl3 adds up. In CHCl₃ the three C–Cl bond moments all lean the same way along the C–H axis, and the H on the opposite side has nothing to cancel them. So it has the largest dipole moment of the four.
Molecule Shape What happens to the bond moments μ (D) NF₃ pyramidal lone pair opposes the N–F moments 0.23 HBr linear one bond, moderately polar 0.79 H₂S bent two S–H moments and lone pairs add 0.95 CHCl₃ tetrahedral three C–Cl moments add, nothing cancels them 1.04 - So. The increasing order is NF₃ < HBr < H₂S < CHCl₃, which is option (c).
The idea to keep. Dipole moment is a vector sum. Check the shape and the direction of every bond moment and lone pair before you trust electronegativity alone.
Answer from the NTA final answer key. Solution by PrepWiser.