Molecular Orbital Theory: Bonding and Antibonding Orbitals

Chemistry · Chemical Bonding · NEET

In Molecular Orbital Theory (MOT), two atomic orbitals combine to make two molecular orbitals. When the electron waves add up (reinforce), you get a low-energy bonding orbital that holds atoms together. When they cancel (subtract), you get a high-energy antibonding orbital (marked with a star, like sigma-star) that pushes atoms apart. Memory hook: "Add = bond, Subtract = star."
Two atomic orbitals combine into two molecular orbitalsAtom A (1s)Atom B (1s)Antibonding (σ*): high energynode between nucleiBonding (σ): low energyelectrons build up between nucleiwaves subtractwaves add
Two 1s atomic orbitals combine to give a low-energy bonding MO (waves add, electrons between the nuclei) and a high-energy antibonding MO (waves subtract, a node forms between the nuclei).

Your doubts, answered

What actually is a bonding orbital vs an antibonding orbital?

Think of electrons as waves. When you bring two atoms close, their orbital waves mix. If the waves add together, electron density builds up BETWEEN the two nuclei. This is the bonding molecular orbital. That extra electron cloud between the nuclei acts like glue, so the orbital has LOW energy and makes the molecule stable. If the waves subtract (cancel), electron density is pushed AWAY from the middle, leaving almost no electrons between the nuclei. This is the antibonding orbital. It has HIGH energy and works against bonding. We mark antibonding orbitals with a star, like sigma-star or pi-star.

Why does an antibonding orbital have a node and higher energy?

A node is a place where the chance of finding an electron is zero. In an antibonding orbital, the two waves cancel exactly at the midpoint between the nuclei, so a node forms right between the two atoms. With no electron glue in the middle, the two positive nuclei feel more repulsion. That is why the antibonding orbital sits HIGHER in energy than the original atomic orbitals, while the bonding orbital sits lower. NEET loves this fact: pi-star has a node between the nuclei.

How many molecular orbitals do I get, and where does the energy go?

A simple rule: the number of molecular orbitals equals the number of atomic orbitals you started with. Combine two 1s orbitals and you get exactly two MOs, one bonding (sigma-1s) and one antibonding (sigma-star-1s). The bonding one drops in energy by some amount; the antibonding one rises by a slightly larger amount. So MOs are always made in pairs, one low and one high.

What is the difference between a sigma MO and a pi MO?

It depends on HOW the atomic orbitals overlap. Head-on (end-to-end) overlap along the bond axis gives a sigma molecular orbital, which is symmetrical around the bond axis. Sidewise (parallel) overlap of p orbitals gives a pi molecular orbital, which has more electron density above and below the axis and is NOT symmetrical around it. This exact point was tested in NEET 2023.

Why does He2 not exist but H2 does?

Fill the MOs with electrons like a ladder, lowest first. H2 has 2 electrons: both go into the bonding sigma-1s, so it is stable. He2 has 4 electrons: 2 fill bonding sigma-1s and 2 fill antibonding sigma-star-1s. The bonding effect is cancelled by the antibonding effect, so bond order is zero and He2 does not exist. This is a classic NEET trap.

Do I have to memorise the MO energy order?

For NEET, yes, learn two orders. For light molecules up to N2 (14 electrons or fewer), the two pi-2p orbitals are BELOW sigma-2pz. For O2, F2 and heavier, sigma-2pz is BELOW the pi-2p orbitals. Getting this order right is exactly what NEET 2023 asked. It also decides magnetism, which the next concept covers.

⚠️ The NEET trap
Students think O2+ is diamagnetic because it 'lost an electron and became stable', or that a pi molecular orbital is symmetrical around the bond axis like a sigma orbital.
O2+ still has one unpaired electron in a pi-star-2p orbital, so it is PARAMAGNETIC, not diamagnetic. And a pi MO comes from sidewise overlap, so it is NOT symmetrical around the bond axis; only sigma MOs are.
🧠 Star does not always mean paired. Count electrons in the pi-star boxes before you call anything diamagnetic.

Real NEET questions

NEET 2023 Phase 2

Which one of the following statements is incorrect related to Molecular Orbital Theory?

A · Molecular orbitals obtained from 2px and 2px orbitals are symmetrical around the bond axis
B · A pi-bonding molecular orbital has larger electron density above and below the internuclear axis
C · The pi-star antibonding molecular orbital has a node between the nuclei
D · In the formation of a bonding molecular orbital, the two electron waves of the bonding atoms reinforce each other
Solution: Sidewise (lateral) overlap of 2px or 2py orbitals gives PI molecular orbitals, which are NOT symmetrical about the bond axis. Only the head-on 2pz overlap gives a sigma MO that is symmetrical around the bond axis. So statement A is the incorrect one. Statements B, C and D are all correct descriptions of MOT.
NEET 2020

Identify a molecule which does not exist.

A · C2
B · O2
C · He2
D · Li2
Solution: Use bond order = 1/2 (Nb - Na). He2 has 4 electrons: 2 in bonding sigma-1s and 2 in antibonding sigma-star-1s, so bond order = 1/2 (2 - 2) = 0. A zero bond order means no net bond, so He2 does not exist. C2, O2 and Li2 all have positive bond orders and do exist.
NEET 2019

Which of the following diatomic molecular species has only pi bonds according to Molecular Orbital Theory?

A · O2
B · N2
C · C2
D · Be2
Solution: C2 configuration is KK (sigma-2s)^2 (sigma-star-2s)^2 (pi-2px)^2 (pi-2py)^2. The sigma-2s and sigma-star-2s cancel, and no electrons sit in the sigma-2pz bonding MO. So its bond order of 2 comes entirely from the two filled pi bonding orbitals, meaning C2 has only pi bonds and no sigma bond.

Solved Chemical Bonding NEET PYQs

Try the real previous-year questions from this chapter — each with the answer and a full solution.

See all 51 Chemical Bonding NEET PYQs ›
Next concept: Bond Order from MOT and Predicting Paramagnetism (NEET)Keep learning — 2 minFeeling ready? Solve the Chemical Bonding NEET PYQs ›Or practice on your phone — get the free MedicNEET app ›

Frequently asked

What is the main idea of Molecular Orbital Theory?

Electrons in a molecule do not belong to one atom. Atomic orbitals combine to form new orbitals called molecular orbitals that spread over the whole molecule. Combining gives one lower-energy bonding orbital and one higher-energy antibonding orbital.

How do you tell a bonding orbital from an antibonding orbital?

A bonding orbital has extra electron density between the nuclei and lower energy. An antibonding orbital has a node (zero electron density) between the nuclei, higher energy, and is written with a star symbol.

Are electrons in antibonding orbitals bad?

They weaken the bond. Every electron in a bonding orbital helps hold the atoms together, and every electron in an antibonding orbital cancels one bonding electron. If both are equal, bond order is zero and the molecule cannot exist.

Why is MOT important for NEET?

MOT explains things VBT cannot, like why O2 is paramagnetic and why He2 does not exist. NEET asks direct questions on MO energy order, bond order and magnetism almost every year in Chemical Bonding.

What comes after learning bonding and antibonding orbitals?

Next you learn to calculate bond order using the formula 1/2 (Nb - Na) and to predict whether a molecule is paramagnetic or diamagnetic from unpaired electrons. That is the next concept in this chapter.