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Last updated 12:03 AM on 6/18/26
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103 Terms

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chemical bond

  • involves the electrons only

  • nuclei of the different atoms are not affected

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Quantum Theory

  • electrically neutral (# of protons = # of electrons)

  • acquire the more stable electron structure of the nearest Noble Gas

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orbital

region of space where electrons are most likely to be found

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non-valance electrons

in the inner energy levels

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valance electrons

  • in the outer shell

  • paired or single

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lone pair

  • two electrons (pair)

  • repelling effect on electrons in any nearby orbitals

  • reduce the bond angle by 2.5°

  • closer to central atom - more repulsion than bonded pairs

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bonding electron

  • single electron

  • share that electron with another atom

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Octet Rule

  • obeyed by Main Group atoms

  • max. eight electrons can occupy orbitals in the valence energy level to become like noble gasses

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Pauli Exclusion Principle

  • two electrons may share the same region of space (never more)

  • occupy empty valence orbitals before forming electron pairs

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Chemical Formulae

  • structure of atoms

  • identify element

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<p>.</p>

.

Molecular Formula - do not reduce

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<p>.</p>

.

empirical formula - reduce

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<p>.</p>

.

Lewis Structure

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<p>.</p>

.

Structural Formula (Kekulé Structure)

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<p>.</p>

.

Perspective Drawing (Stereochemistry)

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<p>.</p>

.

Ball and Stick Model

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rules for placing electrons

  • One electron dot is placed in each of the four valence orbitals before electron pairing

  • If there are five to eight valence electrons, a second electron with a bonding electron

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ionic compound

  • transfer of electrons

  • electronegative atom - anion

  • less electronegative atom - cation

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naming inorganic compounds

  • ionic or molecular

  • ionic - how many ions does the metal form (eg. Cu (ii))

  • monatomic or polyatomic

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NH4+

make ionic compounds due to positive charge

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name → formula

right to left

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formula → name

left to right

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ionic compound shape

  • solid at room temperature

  • form crystal (ionic) lattice

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lewis structure for ionic compounds

  • draw lewis structure of both atoms

  • draw half-headed arrow to show transfer

  • add more atoms to balance the charges

  • draw square brackets around ions and add charges (lost/gained)

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lattice

  • maximize forces of attraction

  • shape of ionic compounds

  • unit cell defined by the lattice points

  • array of alternating positive and negative charges

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properties of ionic compounds

  • lattice

  • high MP and BP

  • non-conductive as solid

  • conductive as molten or in aqueous solution

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high MP and BP

  • strong attraction between cation and anion

  • hard to seperate

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non-conductive as a solid

cation and anion are fixed in the solid state - no movment

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conductive as molten/in solution

cation and anions are free to move

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brittle

  • when knocked out of place, positive aligns with positive, negative aligns with negative

  • repulsion occurs, causing a fracture

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intermolecular forces

  • the forces that exist between molecules

  • London dispersion

  • dipole-dipole

  • hydrogen bond

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intramolecular forces

  • forces that hold atoms together within molecules

  • covalent bonds

  • ionic bonds

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london dispersion

  • temporary

  • non-polar

  • determined by the number of electrons in the molecule

  • low boiling point - weak attraction

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dipole-dipole

  • permanent

  • polar

  • stronger dipole = stronger force

  • attracts positive end with negative end

  • higher boilng point

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hydrogen bond

  • permanent

  • N, O, F is bonded to H

  • strongest of all IMFs

  • high boiling point - strong attraction, hard to break

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covalent bonds

  • atoms share valence electrons

  • non-metal + non-metal

  • non-polar/polar

  • ΔEN less than 1.7

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ionic bonds

  • transfer of electrons

  • ΔEN more than 1.7

  • metal (cation) + non-metal (anion)

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bond strength order (strongest to weakest)

  • metallic

  • ionic

  • molecular

  • hydrogen bonding

  • dipole-dipole

  • london dispersion

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Van der Waals’ Forces

  • define attraction of intermolecular forces

  • London dispersion

  • Dipole-dipole

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LDF causes

  • LDFs are in all atom, ion, and molecule

  • temporary shift, attraction between electron and proton, off when shifts back

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boiling point increase

  • size increase

  • more electrons, more surface area

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strength of LDF

  • number of electrons

  • shape and size

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more electrons

stronger LDF

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shape and size

  • affect how close the molecules approach each other in solid and liquid states

  • closer molecule = stronger attraction/repulsion

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<p>graph</p>

graph

  • top - hydrogen bonding - highest boiling point due to strong attraction

  • drop - only LDFs - lowest boiling point due to weak attraction

  • increasing - LDFs increase attraction with an increase in size (more electrons)

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electrostatic attraction

negative side of the dipole bonds with the unshielded proton

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hydrogen bonding requirements

  • first molecule has hydrogen attatched to a highly electronegative atom (N, O, F) - hydrogen bond donor

  • second molecule has a lone pair on a small highly electronegative atom (N, O, F) - hydrogen bond acceptor

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properties of hydrogen bonded substances

  • increased melting/boiling point

  • increase solubility - like disolves like

  • shape and stability

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key points of IMF

  • boiling points are a measure of IMF

  • IMF increase with polarization (seperation of positive/negative charges) of bonds

  • boiling point increases with molar mass/surface area

  • strength of IMF - LDF < DDF < hydrogen bonding < covalent < ionic < metallic

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molecular

related to/has molecules

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polarity

  • contrasted properties/direction

  • having poles

  • opposite powers in opposite parts/directions

  • being opposite

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dipole moments

  • separation of charge

  • large difference in electronegativity = large dipole moment

  • ionic/covalent bond

  • measure polarity

  • electrons unequally shared

  • one atom is more electronegative than another

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shape and polarity of bonds

  • determines overall polarity

  • asymmetrical = polar

  • symmetrical = non-polar

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determinations for polar molecules

  • charges cannot cancel out

  • unequal distribution of charge

  • may include lone pairs

  • may have different types of bonds

  • asymmetrical

  • different peripheral atoms

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Electron Domain

region around the central atom of a molecule where electrons are concentrated

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Bonding Domains

  • single, double, or triple bonds connected to the central atom

  • every bond counted as only one electron domain

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Non-Bonding Domains

lone pairs connected to the central atom

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<p>.</p>

.

Triganol planar

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<p>.</p>

.

linear

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<p>.</p>

.

tetrahedral

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<p>.</p>

.

Triganol pyramidal

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<p>.</p>

.

bent

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VSEPR Theory

  • shape of an atom

  • due to the repulsions between electron pairs in the valence shell

  • depends on number of bonding groups and non-bonding electrons

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number of electron pairs

determined by writing the Lewis structure

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strength of repulsion (highest to lowest)

  1. lone pair - lone pair

  2. lone pair - bonded pair

  3. bonded pair - bonded pair

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AXmEn

  • A = central atom

  • X = bonded/peripheral atom

  • E = lone pairs

  • m and n = number of lone pairs or bonded atoms

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Electronegativity

ability of an atom to attract electrons in a chemical bond

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down a group

  • Atomic radius increases (bigger)

  • Increase in nuclear charge is too small to be important

  • More shielding - more shells

  • electronegativity decreases

  • Less attraction between nucleus and bonding electrons

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shielding effect

  • block

  • inner electrons shields outer electrons from attractive force of the nucleus (protons)

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going across a period

  • atom becomes smaller

  • nuclear charge increases

  • atomic radius decreases

  • greater attraction between nucleus and bonding electron

  • electronegativity increases

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nuclear charge

greater than repulsion charge

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smaller atom

  • more electrons being put in the same energy level

  • less shielding

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sharing

not equal

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non polar covalent electronegativity

  • no pull

  • equal

  • ΔEN - ≤ 0.4

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polar covalent electronegativity

  • higher electronegativity

  • pulls electron towards it

  • 0.4 < ΔEN > 1.7

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ionic bond electronegativity

ΔEN - 1.7 <

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polar covalent

  • between two extremes

  • electron sharing unequal

  • electron density greater around more electronegative atom

  • different non-metals - different electronegativity

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nonpolar covalent

  • same or different non-metals that have same/similar electronegativity

  • electron shared equally

  • purely covalent

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Electrical Charge

  • deficiency/excess of electrons in a chemical species

  • result is a net positive charge or net negative charge

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Molecular Polarity

  • electrical charge not symmetrically distributed among the atoms in a molecule

  • partial positive and partial negative charges on opposite ends of the molecule

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𝛿

  • lower case delta

  • partial charge

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Metallic Bond

sharing of free electrons among a structure of positively charged ions

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No Bond

  • Noble Gases have a full outer valence shell

  • non-reactive

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theory of covalent bonding

  • fill their valence orbitals (except H, He, Be, and B)

  • bonding is attraction of a pair of shared electrons

  • Unpaired electrons can bond

  • Two atoms with bonding electrons form covalent bond

  • The number of covalent bonds that each atom forms is limited (fill valence shell)

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limitation for octet rule

  • first period - only two electrons

  • B and Be - do not need full valance shell

  • odd number of valence electrons

  • third period < exceed rule

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Noble Gases

  • similar properties

  • low reactivity

  • don’t form bonds

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halogens

  • highly reactive

  • need one more electron

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Nomenclature

  • naming chemical compounds

  • easily identified as separate chemicals

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covalent nomenclature

  • least electronegative element first

  • second element - suffix to –ide

  • USE prefixes

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one

mono

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two

di

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three

tri

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four

tetra

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five

penta

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six

hexa

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seven

hepta

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eight

octa

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nine

nona

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ten

deca