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intramolecular forces
bonding forces that occur within a molecule or compound
bonds in molecules
covalent bonds
bonds in ionic compounds
ionic forces
bonds in metals
metallic bonds
water molecule bonds
2 hydrogen atoms are covalently bonded to an oxygen atom in one single unit
attraction between water molecules
attract each other to form larger volumes through IMFS
intermolecular forces
attractive forces between molecules
cohesive forces
attractive forces between the same chemical species
example of cohesive forces
water is attracted to itself, allowing water to form droplets
adhesive forces
attractive forces between different chemical species
example of adhesive forces
water is attracted to cellulose which helps trees absorb water
electrostatic forces of attraction
all IMFS are caused by electrostatic forces of attraction
Coulumb’s law strikes again!
causes of intermolecular and intramolecular bonding
coulombic attraction between the charged particles
strength of intramolecular and intermolecular forces
intermolecular forces are much weaker than intramolecular forces, because the charges are smaller and the distances are greater between molecules
3 states of matter
solid, liquid, or gas
properties of matter in solid form
particles are close together and held in fixed position (low entropy) for attractive forces
vibrate in place and individual atoms have limited movement
properties of matter in liquid form
Particles easily slide past each other
Attractive forces frequently break and reform
The volume is constant
The shape depends on the container
properties of matter in gas form
particles are in constant, independent motion
attractive forces are very low - no fixed position or volume
gasses are extremely compressible
compressibility
measure of how much a substance’s volume can be decreased when pressure is applied
2 formations of solids
amorphous: solid that doesn’t have orderly arrangement of particle
crystalline: solid containing orderly repetitive pattern of particles
4 types of solids
ionic, molecular solids, network covalent solids, metallic solids
bonds in ionic compounds
ionic bonding forces
bonds in molecular solids
intermolecular forces
bonds in network covalent solids
covalent bonding forces
SOMETIMES IMFS but not too common
bonds in metallic solids
metallic bonding forces
ionic compounds composition
crystalline solids of cations and anions
examples of ionic compounds
NaCl, Mg(OH)2
properties of ionic compounds
strong, brittle, dissolve into cations and anions, low vapor pressures, high melting and boiling point
comparing attraction in ionic compounds and covalent bonds
electrostatic attraction in ionic compounds stornger than IMF forces in covalent bonds
factors determining strength of ionic compounds
distance between ions and charge of the ions (coulumb’s law)
molecular solids composition
intermolecular forces (weaker than ionic solids)
examples of molecular solids
ice, dry ice, iodine, sulfur
properties of molecular solids
amorphous/crystalline, low melting + boiling, poor conductors
network covalent solids composition
solid structure composed of a large amount of nonmetals and/or metalloids held together through covalent bonds
examples of network covalent solids
diamond, graphite, silicon dioxide, silicon carbide
properties of network covalent solids
amorphous/crystalline, strong material, high melting + boiling, poor conductor
allotropy
different forms at which chemical elements can be arranged
examples of allotropes
diamond and graphite are allotropes of carbon
2D network solids
atoms are connected through covalent bonds in 2D network
IMFS hold 2D networks
3D Network Solid
atoms that are connected through covalnet bonds in a 3D network
(locked in place and very STRONG)
metallic solid composition
solid made of metallic protons immersed in a sea of delocalized electrons
examples of metallic solid
lithium and iron
metallic solid properties
crystalline solid, malleable, ductile, good conductors
general chemical formula of molecular solid
nonmetals
general chemical formula of network solids
metalloids
general chemical formula of ionic compounds
metal and nonmetal and/or polyatomic ion
general chemical formula of metals
metals
causes of a phase change
energy is added or removed - attractive forces to break apart or come together
stronger the attractive force
the more energy required to break the force
strength of the force depends on
the types of chemical bonds and the composition and positions of the interacting particles.
london dispersion forces
attractive forces between all substances that result from the motion of electrons
electrons are in constant movement
not always evenly dispersed around a chemical species.
Temporary dipole
A temporary attractive force caused by the temporary positions of electrons
Polarizability
The tendency for a molecule to produce more dipole interactions
Polarizability increases with the size of the electron clouds of the molecules
strength of the london dispersion forces in a substance depends on the polarizability of the electrons
concept for polarizability
The larger the electron clouds, the further the electrons are from the nucleus, and the easier the electrons can polarize
increase in mass, surface area, or pi bonds
more chances for electron clouds to form dipoles and strength increases
LDFs in heavier molecules (mass)
LDFs are strongest IMFS due to the large volume of electron clouds
LDFS with surface area
butane has a higher surface area which causes it to have a higher melting and boiling point
LDFs with pi bonds
compounds with higher pi bonds will have higher melting + boiling points due to the pi bonds having more electron orbital overlap and electrons closer together to each other
effect of pi bonds
increase electron density and electron interactions
dipole interactions
attractions between chemical species where at least one of the species is a polar molecule
general types of dipole interactions
dipole-induced interactions
dipole-dipole
ion-dipole
dipole induced interactions
temporary dipole induced from a polar molecule interacting with the electrons in a nonpolar molecule
dipole-dipole
intermolecular forces between polar molecules that form from coulombic attractions between partially positive and partially negative parts of molecules
ion dipole
attraction between a dipole from a molecule and the charge of an ion
at similar molar masses, molecules with dipole-dipole forces are stronger than molecules with only LDFs
molecules with dipole-dipole also contain LDFs, increasing the total strength
polar molecules dissolve
polar molecules
example of polar molecules dissolving polar molecules
Water will dissolve sugar more easily than it will dissolve flour. Sugar has a higher polarity than flour
the strength of dipole-dipole interactions increases with
magnitude and positions of the dipoles
example of dipole-induced dipole
Oxygen is nonpolar, but is able to dissolve in water
The movement of electrons in an oxygen molecule can cause a temporary attraction to the partial positive and negative charges to each other
strength of dipole-induced dipole
strength increases with the polarity of the molecule and the polarizability of the nonpolar molecule
hydrogen bonds
extremely strong type of dipole-dipole force that exists between polar molecules with a hydrogen atom attached to an oxygen, nitrogen, or fluorine atom
cause of strength of hydrogen bonds
hydrogen only has one electron and as the electron spends more time near an electronegative atom, the proton becomes more exposed and is more attracted to electronegative atoms
hydrogen bonds and chemical bonds
even though it is a strong intermolecular force, it is much weaker than chemical bonds
explanation for why water is liquid at room temperature
hydrogen bonding
properties of water attributed to polarity and strong hydrogen bonds
universal solvent, highly polar, expands when frozen, found as liquid/solid/gas
gravitational forces compared to ion-dipole forces
ion-dipole forces are stronger than gravitational forces
strength of IMFS at similar masses
ion-dipole, hydrogen bonds, dipole-dipole, london dispersion
if molecules have the same types of IMFS
strengths increase with mass and complexity.
properties that increase with strengthening attractive forces
melting/boiling point
heat of vaporization and heat of fusion
surface tension
viscosity
capillary action
vapor pressure
volatility
solubility
melting and boiling point
temperature at which a substance changes phases
heat of vaporization and heat of fusion
amount of energy rquired for a substance to change phases
causes of phase changes
when attractive forces break
surface tension
amount of energy required to increase the surface area
liquid molecules minimize surface area
stronger attractive forces are more likely to pull liquid into a sphere
viscosity
tendency for a liquid to resist flow
viscosity explanation
when attractive forces are stronger, particles are strongly attracted to each other and don’t flow around each other easily
capillary action
rise of a liquid due to the interaction between cohesive and adhesive forces
explanations for capillary action
capillary action increases with increasing adhesive attractions
vapor pressure
pressure applied from the collisions of vaporized particles in equilibrium within its liquid phase
explanations for vapor pressures
in a closed container, molecules with weaker IMFS will not evaporate as frequently and there will be less overall collisions
volatility
how easily a substance evaporates
takes less time to evaporate when the molecules are less attracted to each other
solubility
maximum amount a substance will dissolve in a solvent
relation of solubility with cohesion and adhesion
solubility decreases with increasing cohesive strength and decreases with adhesive strength
kinetic molecular theory of gasses
gasses are made of particles with no volume
no attractive or repulsive forces
particles are in constant random motion
collisions are elastic
kinetic energy is directly proportional to the temperature
gasses are compressible
volume of gas depends on size of the container
gas described by 4 properties
volume (amount of space a container takes up)
molar amount (amount of particles in the sample)
temperature (average kinetic energy of the particles)
pressure (force of particles exerted over an area)
gas laws
group of laws in the form of equations that state the relationships between gas properties in an ideal gas
kinetic molecular theory defines volume of an individual gas particle as 0
this is because particles in the gas phase are so far apart from each other
as more particles are added to a group of particles
the volume will expand