Structure and Bonding Flashcards
Definitions
- protons and neutrons
- electron cloud
- mass (nucleus)
- volume (electron)
Atomic Structure
two or more forms of the same element that contain equal numbers of protons but different numbers of neutrons
Isotopes
electron location unknown but electron density is known
Quantum Mechanical Model
electron will be in a certain region of space (orbital) at a given instant
Electron Density
Electrons do not circle around the nucleus in fixed orbits but rather,
in ________.
Orbitals
Each orbital has a characteristic _____and ____ (energy).
Shape and Size
used to described orbitals
Quantum Numbers
lowest-energy orbitals fill up first
Aufbau Principle
If two or more empty orbitals of equal energy are available, one electron occupies each with spins parallel until all orbitals are half-full,
Hund’s Rule
Only two electrons can occupy an orbital, and they must
have opposite spins
Pauli’ Exclusion Principle
there is a limit to the precision with which certain pairs of physical properties can be simultaneously known
Heisenberg’s Uncertainty Principle
Electron BELOW the outermost shell
Core Electrons
Electrons IN the outermost shell
Valence Electrons
An attractive force between two ions or between two atoms
Chemical bond
Why do chemical bonds form?
more stable and lower in energy
How do chemical bonds form?
Octet Rule
Chemistry of main-group elements is governed by their tendency to
take on the electron configuration of the nearest noble gas.
Octet Rule
Attractive forces between opposite charges
Electrostatic Attraction
formed in electrostatic attraction
formed in transfer of electrons
reaction of metals with nonmetals
Ionic Bond
Compounds formed by ionic bonds
Ionic Compound
Bond formed as a result of sharing electrons between two nuclei
Covalent Bond
Compounds formed by covalent bonds
Molecular compounds
Measure of the ability of an atom to pull the bonding electrons toward itself
Electronegativity
covalent bond between atoms with SAME electronegativity
Nonpolar covalent bond
covalent bond between atoms with DIFFERENT ELECTRONEGATIVITIES
Polar covalent bond
< 0.4
pure covalent
between 0.4 and 1.8
Polar covalent
> 1.8
ionic
a pair of equal and oppositely charged poles separated by a DISTANCE
Dipole
Measure of Dipole
Dipole moment
magnitude of the charge on either atom x distance between the two charges
Dipole moment
electron-dot structures
Lewis Structures
line-bond structures
Kekule Structures
not an actual charge, used for bookkeeping of electrons
Formal charge
charge if each bonding electron pair in the molecule were shared equally between atoms
Formal Charge
Difference VE when it is not bonded and VE when it is bonded
Formal Charge
OMITTING OF THE COVALENT bonds and listing
atoms bonded to a particular carbon (or nitrogen or oxygen) next toit (with a subscript if there is more than one of a particular atom)
Condensed structures
C atoms aren’t shown
C atoms are assume in the lines
H atoms aren’t shown
Atoms other than C and H are shown
Skeletal structures
Shows 3D shape
Perspective Drawing
Show bond angles accurately
Ball-and-Stick Model
Shows atoms in scale
Space-filling Model
Bond lies in the plane of the paper
Normal Bond
Bond extends backwards, away from the viewer
Dashed bond
Bond protudes forwards, toward the viewer
Wedged bond
Geometry based on arrangement of atoms in a molecule + defined by bond angles
Molecular Geometry
Geometry based on valence electron pairs around a central atom + Defined by bond angles
Electron pair geometry
A model for the prediction of molecular geometry based on the MINIMIZATION OF ELECTRON REPULSION between regions of eelctron density around an atom
Valence-Shell Electron-Pair Repulsion Model (VSEPR)
The best arrangement of a given number of electron pairs (bonding and nonbonding) is the one that minimizes the repulsions among them.
Valence-Shell Electron-Pair Repulsion Model (VSEPR)
Without lone pairs:
Electron Pair Geometry and Molecular Geometry is equal
assumes that the electrons in a molecule occupy OVERLAPPING atomic orbitals of the individual atoms
Valence Bond Theory
Assumes the formation of molecular orbitals from the atomic orbitals
Molecular Orbital Theory
How is covalent bonds formed?
When atomic orbitals on neighboring atoms overlap one another
head-on overlap of atomic orbitals; stronger
Sigma σ
sideway overlap of atomic orbitals; weaker
PI BONDS (π)
atomic orbitals obtained when TWO OR MORE NONEQUIVALENT ORBITALS of the SAME ATOM combine for covalent bond formation
Hybrid Orbitals
Produces the molecular geometry of the molecule.
Hybridization
The greater the electron density in the gregion of orbital overlap
The stronger and shorter the bond
As s character increases, bond angle _______
Increases
Describes a region of space in a molecule where electrons are most likely to be found
Molecular Orbital
2 ways to combine atomic orbitals into molecular orbitals
Additive and Subtractive
2 ways to combine atomic orbitals into molecular orbitals
? - Lower energy, bonding molecular oribtal
Additive
2 ways to combine atomic orbitals into molecular orbitals
? - higher energy, antibonding molecular orbital
Subtractive
occurs when an electron is shared by more than 2 atoms with π bonds (p orbitals)
π ELECTRON DELOCALIZATION
Structures are represented by resonance contributors
π ELECTRON DELOCALIZATION
Some substances can’t be represented by a single line-bond structure and must be considered as a resonance hybrid of two or more structures.
Resonance
two individual line-bond structures
Resonance forms
indicated by the double-
headed arrow between them.
Special Resonance Relationship
What is the different between resonance forms?
Placement of the π BOND and NONBONDING VALENCE ELECTRONS
single unchanging structure
Resonance Hybrid
two individual forms and has characteristics of both
Resonance Hybrid
Between resonance forms
Double headed arrow
Movement of electrons
Curly Arrow
From electron-rich species
Tail
To electron-deficient specials
Head
Double bonds separated by single bonds
Conjugation
Refers to a system that has a p orbital adjacent to a π bond allowing delocalization of π electrons
Conjugation
Compounds with isolated double bonds (___________)
Higher energy
Special kind of conjugation and cyclic unsaturated molecules with unusual stability
Aromaticity
Originally used to classify benzene and its derivatives because
many of them have distinctive odors
Aromaticity