Chemical Bonding Textbook Notes

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Chemical Bonding

as pKa decreases, acidity increases!

Molecular Orbital Theory: hybrid orbitals Valence Bond Theory: a chemical bond is
are formed by mixing different types of formed when the orbitals of two atoms
atomic orbitals, such as s and p orbitals. these overlap and share electrons (de-localised)
hybrid orbitals then overlap with other atomic
covalent bond forms when the atomic
orbitals to form molecular orbitals. (creating
orbitals of two atoms overlap
new shapes, energy levels, and de-localised
electrons)

ex. methane: the compound undergoes


hybridisation, forming four sp^3 bonds,
these orbitals overlap with the 1s orbital
and forms a molecular orbital

De-localised Electrons:
localised charges - electrons cannot move
from atom

localised electrons are less stable than


de-localised electrons as one atom is
bearing the whole negative charge

de-localised charges - electrons are shared


Hybrid Orbital: an orbital that is formed by and can move freely between multiple atoms
mixing different types of atomic orbitals. (mostly between metallic elements)
ex. methane: the carbon atom undergoes atoms that share electrons are now either
hybridisation and forms four sp^3 hybrid both negative or both positive
orbitals. These hybrid orbitals are a
electrons that make up the double bond
combination of one s orbital and three p
are shared equally between all atoms

Chemical Bonding 1
orbitals. The four sp3 hybrid orbitals of (any compound with a double bond has
carbon overlap with the 1s orbitals of the de-localised electrons)
hydrogen atoms, resulting in four strong
conjugated double bonds: double
sigma bonds. This arrangement gives
bonds that share electrons
methane its tetrahedral shape.
VSEPR Theory: A theory that predicts three-
dimensional arrangements of electron groups
around a central atom based on electron
group repellent forces, like the distance of
electron groups (in degrees); a model used to
predict molecular shapes.
Resonance Structures: only can be drawn if
electrons are de-localised

these structures are indicated by double


headed arrows ↔

major resonance contributors are


determined by which structures is more
stable with the negative charge

ex. oxygen with a negative charge is


more stable than carbon due to
electronegativity

major structures - determined by where the


+/- charge is located

tertiary →secondary→primary (stability


chart)

Chemical Bonding 2

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