Chapter 9 Covalent Bonding: Orbitals. Schroedinger An atomic orbital is the energy state of an...

Chapter 9

Covalent Bonding: Orbitals

Schroedinger

An atomic orbital is the energy state of an electron bound to an atomic nucleus

Energy state changes when it is bonded to another atom

Hybridization is the combining of wave functions to give new wave functions

http://www.mikeblaber.org/oldwine/chm1045/notes/Geometry/Hybrid/Geom05.htm

9.1 Hybridization and the Localized Electron Model

Localized electron model - a molecule is a collection of atoms bound together by sharing electrons

A modification of the LE model is needed to account for the type and arrangement of bonds actually seen in molecules

A molecule is more than the sum of its parts. It tries to achieve minimum energy

Hybridization – mixing of “native” atomic orbitals to form special orbitals for bonding

Localized model

Write the Lewis structure Determine the best arrangement using

VSEPR Determine the hybrid atomic orbitals

necessary (apply to peripheral and central atoms)

Electron pairs (lone pairs) not involved in bonding may occupy hybrid orbitals.

Atoms adjust to minimize energy and electron pair repulsions.

The whole molecule is considered rather than the individual atom.

Effective pairs – lone, single or multiple bonds

sp3 hybridization

Energy between 2s and 2p The new orbitals are four identically shaped

orbitals (Fig. 9.3 p. 405) They are oriented towards the corners of a

tetrahedron Account for known structure

One 2s orbital and three 2p orbitals combine to form four new sp3 orbitals (s1p3)

Assume bonding only involves valence electrons

The total number of electrons and their arrangement in the molecule is important

Atomic orbitals are arranged to accommodate the best electron arrangement for the molecule as a whole

sp3 hybridization gives 4 identical orbitals

*Whenever a set of equivalency tetrahedral atomic orbitals is required by an atom, the atom adopts a set of sp3 orbitals.

Ex. C has 2s2 2p2 valance electrons

sp2 hybridization

For three bonds or effective pairs Trigonal planar shape Combine one s and two p orbitals The plane is determined by the p orbitals

(x,y,z)

sp2 hybridization gives three identical orbitals

whenever an atom is surrounded by three effective pairs, a set of sp2 hybrid orbitals is required.

One p orbital remains unchanged

Sigma(s) bond

the electron pair is shared in an area centered by the line running between the atoms

formed from orbitals whose lobes point towards each other

(pi) bonds

sharing an electron pair in the space above and below the sigma bond

Unhybridized p orbitals form pi bonds use the 2p orbital perpendicular to the sp2

hybrid

So…

A double bond consists of a sigma bond and a pi bond

Ethylene (C2H4)

sp hybridization

One s and one p orbital 1800 apart Two effective pairs around an atom Linear Two p orbitals remain unchanged; they are

used for pi bonds

dsp3 hybridization

When a central atom exceeds the octet rule One d, one s, and three p orbitals When five electron pairs need to be

represented Trigonal bipyramidal arrangement

d2sp3

Six electrons pairs around the central atom

Octahedral arrangement

Summary

Hybrid orbitals demo

Problems p. 431 # 24, 29 hybrid orbitals P. 432 # 33, 35, 37 sigma, pi bonds

9.2 The Molecular Orbital ModelLE model problems: Incorrectly assumes electrons are localized Needs the concept of resonance Unpaired electrons are a problem Gives no information about bond energies

Molecular Orbital Model

(We don’t know exactly where electrons are, so we can’t accurately predict interactions)

Compare predictions with experimental observations. MO’s are like atomic orbitals Hold two electrons with opposite spins Square of the MO wave function indicates electron probability Always the same number of atomic orbitals as the sum of the atoms

that formed them

Ex. 2H H2

 Each H has a 1s atomic orbital Quantum mechanical equations give two

molecular orbitals  MO2 = 1SA – 1SB

MO1 = 1SA + 1SB

The greatest probability for MO1 is between the nuclei.

MO2 is on the outside of each nuclei. Distribution is called sigma (like LE) molecular orbitals.

(Atomic orbitals no longer exist.) MO1 is lower in energy than 1s atomic, MO2 is higher

Electrons in MO1 favor bonding, MO2 are anti-bonding.

Bonding are lower energy since they are attracted by both nuclei.

MO designations include shape, original (parent) atomic orbitals and bonding/anti-bonding properties.

For 2p: The overlapping pair produces one bonding

and one anti-bonding sigma molecular orbital The parallel pairs produce two bonding and

two antibonding p MO’s.

Ex. For H

MO1 = 1s

MO2 = 1s*

(* designates anti-bonding) Molecular electron configurations – written

like electron configurations

  H2 (1s )2

Bond Order

difference between the number of bonding and the number of anti-bonding electrons divided by two.

(Two is used because bonds represent pairs of electrons.)

Is an indication of bond strength Larger bond order means greater bond strength A value of zero is unstable

Problems

p. 433 # 39,41

9.3 Bonding in Homonuclear Diatomic Molecules Two identical atoms Consider elements in period 2  Only the valence electrons contribute to molecular

orbitals. (Core levels are smaller and the electrons are

considered to be localized.) You can determine if a molecule is stable or if it exists

based in bond order.  Metals also form metallic bonds of many atoms.

Magnetic properties

Most substances do not exhibit magnetism unless they are in a magnetic field.

A. Paramagnetism – a substance is attracted into the inducing magnetic field

B. Diamagnetism – a substance is repelled from the inducing field.

A substance is weighed both with and without a magnetic field. If the weight increases, it is paramagnetic.

Unpaired electrons –

paramagnetic properties (oxygen)

Paired electrons – diamagnetic properties 

If both conditions exist, there is a net paramagnetic effect since this is stronger.

Boron needs to use s-p mixing to explain its magnetic properties.

Energy of 2p and 2p are reversed.

Summary

As bond order (predicted) increases, bond energy increases and bond length decreases.

  Bond order is not associated with particular

bond energy.

  N2 has a triple bond, bond order 3. In

explosives, much energy is released from N containing compounds as N2 is formed.

O2 is paramagnetic as predicted from MO theory. LE theory predicts diamagnetic.

bond order = (bonding – anti bonding) / 2

  You need to get electron configurations using

MO’s and then use bond order to determine the strongest bond.

Samples Problems p. 433 #47, 48

9.4 Bonding in Heteronuclear Diatomic molecules Heteronuclear – different atoms

  If the atoms are close on the periodic table,

use the MO for homonuclear molecules.

  When the atoms are very different, a new

energy diagram is necessary for each molecule.

The sigma bond would show greater probability close to the atom with an orbital of lower energy. This would produce a polar bond.

9.5 Combing the localized Electron and Molecular Orbital ModelsLE : Electrons are localized Resonance is necessary to explain some

bond angles More than one valid Lewis structure can be

drawn for some molecules

MO : allows for delocalization

Combine LE and MO for molecules that require resonance structures.

Ex. A double bond that could be in more than one location becomes one and one bond to give the most physically accurate description of the molecule.

  LE describes the MO describes the

Ex. Benzene C6H6

6 equivalent C-C bonds All the atoms are in the same plane sp2 orbitals – sigma bond p orbitals perpendicular to the plane for

orbitals Gives delocalized

bonding

Additional exercises

p. 447 # 51, 55, 57 Challenge # 61