Chapter 11- Liquids and Intermolecular Forces and Chapter 12- Solids and Modern Materials

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Particle arrangement in solids

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Particle arrangement in solids

closely packed in an ordered array; positions are essentially fixed; energies of particle-particle attraction are greater than kinetic energies of particles

<p>closely packed in an ordered array; positions are essentially fixed; energies of particle-particle attraction are greater than kinetic energies of particles</p>
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Particle arrangement in liquids

particles are closely packed but randomly orientated; retain freedom of motion; kinetic energies of particles similar to energies of particle-particle attraction

<p>particles are closely packed but randomly orientated; retain freedom of motion; kinetic energies of particles similar to energies of particle-particle attraction</p>
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Particle arrangment in gas

particles are far apart; posses complete freedom of motion; kinetic energies of particles are greater than the energies of particle-particle attraction

<p>particles are far apart; posses complete freedom of motion; kinetic energies of particles are greater than the energies of particle-particle attraction</p>
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Ion-Dipole Forces

interaction between an ion and a dipole; a neutral, polar molecule (ex: water); strongest of all intermolecular forces (solutions ONLY)

<p>interaction between an <em>ion</em> and a <em>dipole</em>; a neutral, <strong>polar molecule</strong> (ex: water); strongest of all intermolecular forces (solutions ONLY)</p>
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Dipole-Dipole Forces

between neutral polar molecules (oppositely charged ends of molecules attract); weaker than ion-dipole forces; increase with increasing polarity; strength of attractive forces is inversely related to molecular volume

<p><strong>between neutral polar molecules</strong> (oppositely charged ends of molecules attract); weaker than ion-dipole forces;<strong> increase with increasing polarity; strength of attractive forces is inversely related to molecular volume</strong></p>
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London Dispersion Forces

weakest of all intermolecular forces; two adjacent neutral, nonpolar molecules; the nucleus of one attracts the electrons of the other; electron clouds are distorted; instantaneous dipole; strength of forces is directly related to molecular weight; exist between all molecules; depend on the shape of the molecules; the greater the surface area available for contact, the greater the force is

<p>weakest of all intermolecular forces; two adjacent <strong>neutral, nonpolar molecules</strong>; the nucleus of one attracts the electrons of the other; electron clouds are distorted; instantaneous dipole; strength of forces is directly related to molecular weight; exist <strong>between all molecules; </strong>depend on the shape of the molecules; the greater the surface area available for contact, the greater the force is</p>
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Hydrogen Bonding

special case of dipole-dipole forces; H-bonding requires H bonded to an electronegative element (F, O, N); boiling increases with increasing molecular weight (exception water)

<p>special case of dipole-dipole forces; H-bonding requires <strong>H bonded to an electronegative element </strong>(F, O, N); boiling increases with increasing molecular weight (exception water)</p>
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Intermolecular Forces

London dispersion forces, dipole-dipole forces, hydrogen bonding, ion-dipole forces, ionic bonding

<p>London dispersion forces, dipole-dipole forces, hydrogen bonding, ion-dipole forces, ionic bonding</p>
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What is the effect of molar mass on IMFs?

increasing molar mass has stronger IMFs

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What is the effect of structure on IMFs?

longer molecules have a greater surface area result in stronger IMFS

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11

The stronger the attractive forces, the (boiling point and melting point)

the higher the boiling point of the liquid and the melting point of a solid

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12

Temperature of boiling point increases as pressure

decreases

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high altitude: low pressure so water boils at

lower temperature

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liquids boil when the external pressure equals

the vapor pressure

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Normal boiling point

Boiling point of a liquid at 1 atm

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Vapor Pressure

pressure exerted when the liquid and vapor are in dynamic equilibrium; some molecules on the surface of a liquid have enough energy to escape to the gas phase, after some time the pressure of the gas will be constant at the vapor pressure (equilibrium)

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Dynamic Equilibrium

the point when as many molecules escape the surface as strike the surface

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Vapor Pressure increases nonlinearly with increasing

temperature (Clausius-Clapeyron Equation)

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If equilibrium is never established then the liquid

evaporates; volatile substances (high VP) evaporate rapidly

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the higher the temperature, the higher the average KE, the _____ the liquid evaporates

faster; (hot water is even faster than cold water)

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Volatility

liquids that evaporate readily

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What is the effect of IMFs on vapor pressure?

stronger the forces, the lower the vapor pressure; inverse relationship; fewer molecules will have enough KE to escape and substances with high vapor pressures are volatile, easily evaporate

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What is the effect of surface area on vapor pressure?

no effect

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Viscosity

resistance of a liquid to flow; molecules slide over each other

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What is the effect of temperature on viscosity of a substances?

inverse relationship; viscosity decreases with increased temperature; increasing temperature increases energy and the velocity, so they interact for shorter time reducing internal friction and decreasing viscosity

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What is the effect of molecular weight on viscosity of a substances?

viscosity increases with an increase in molecular weight; proportional

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What is the effect of IMFs on viscosity of a substances?

the stronger the intermolecular forces, the higher the viscosity; proportional

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Meniscus formation and characteristics

when adhesive forces are greater than cohesive forces, the water binds to the graduated cylinder creating a U-shaped meniscus; if the cohesive forces are greater, then the water binds to itself creating a curved downwards meniscus

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Adhesive forces

bind molecules to a surface

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Cohesive forces

bind molecules to each other

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Surface Tension

amount of energy required to increase the surface area of a liquid

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Phase Changes

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Generally the heat of fusion is less than

the heat of vaporization; takes more energy to completely separate molecules, than to partially separate them

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What is the term for melting?

heat of fusion

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What is the term for evaporation?

the heat of vaporization

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Vaporization

endothermic; liquid → gas

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Melting

endothermic; solid→liquid

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sublimation

endothermic; solid→gas

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condensation

exothermic; gas→liquid

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freezing

exothermic; liquid→solid

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deposition

exothermic; gas→solid

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Heating curve

plot of temperature change vs. heat added; during a phase change, adding heat causes no temperature change (equilibrium); points calculate change in Hfus and change in Hvap

<p>plot of temperature change vs. heat added; during a phase change, adding heat causes no temperature change (equilibrium); points calculate change in H<sub>fus</sub> and change in H<sub>vap</sub></p>
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43

Gases are liquefied by increasing __________ at some temperature

pressure

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critical temperature

the minimum temperature for liquefaction of a gas using pressure; high CT means strong intermolecular forces

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Critical pressure

pressure required for liquefaction

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Exothermic

transfers heat or the surroundings; feels hot

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Endothermic

absorbs heat from surroundings; feels cold

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Coulomb’s Law

the strength of the electrostatic force (attraction/repulsion) between two charged objects; higher charges, higher electrostatic forces. longer distances, lower electrostatic forces

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Metallic solids

held together by a “sea” of collectively shared electrons

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Ionic soldis

sets of cations and anions mutually attracted to each other (Coulomb’s Law)

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Covalent-network soldis

joined by an extensive network of covalent bonds

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molecular solids

discrete molecules held together by weak forces

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Metal

group of cations suspended in a sea of electrons (electron-sea model)

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Alloys

materials that contain more than one element and have characteristic properties of metals; employed to change the properties of certain metals

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Substitutional alloys

second element takes the place for a metal atom; homogeneus mixture; components dispersed randomly and uniformly; atoms of solid occupy positions occupied normally by a solvent atom; 2 metallic components with similar atomic radii and chemical-bonding characteristics

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Interstitial alloys

second element fills a space in the lattice of metal atoms; homogeneous mixtures; components dispersed randomly and uniformly; atoms of the solute occupy positions in the “holes” between solvent atoms; solute atoms need to have smaller bonding atomic radius than solvent atoms; its element is a nonmetal that makes covalent bonds with the metal atoms; harder, stronger, less ductile

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Heterogeneous alloys

components not dispersed uniformly; components are not dispersed uniformly; properties depend on the composition and manner when a solid is formed from molten mixture; formed by rapid cooling are different from slow cooling of same mixture

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Properties of Ionic Solids

very high melting and boiling points; quintessential crystals; charge is centered on the anions, electronic insulators; favorable Structures with hcation-anion distances as close as possible; CsCl structure, NaCl structure and Zince blende (ZnS) structure

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cesium chloride (CsCl) structure; primitive cubic lattice

two atom-basis; center atom; no lattice point inside primitive unit cell; anions sit on the lattice points at the corners and cations sit in the center of the cell; surrounded by 8 atoms;

<p>two atom-basis; center atom; no lattice point inside primitive unit cell; anions sit on the lattice points at the corners and cations sit in the center of the cell; surrounded by 8 atoms; </p>
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60

Sodium Chloride (NaCl); rock salt structure

face-centered cubic lattice; anions sit on lattice points that lie on the corners and faces of unit cell; cations are displaced from anions along the edge of the unit cell; each cation and anion are surrounded by six ions of the opposite type; octahedral coordination environment

<p>face-centered cubic lattice; anions sit on lattice points that lie on the corners and faces of unit cell;  cations are displaced from anions along the edge of the unit cell; each cation and anion are surrounded by six ions of the opposite type; octahedral coordination environment</p>
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61

Zinc blende (ZnS)

face-centered cubic lattice; anions sit on the lattice points that lie on the corners and faces of the cell; cations are displaced from anions along the body diagonal of the cell; each cation and anion are surrounded by 4 of the opposite type; tetrahedral coordination geometry

<p>face-centered cubic lattice; anions sit on the lattice points that lie on the corners and faces of the cell; cations are displaced from anions along the body diagonal of the cell; each cation and anion are surrounded by 4 of the opposite type; tetrahedral coordination geometry</p>
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62

When to use the ionic structure based on ion size?

cation and anion are similar in size, large coordination # is favored so CsCl structure; relative size of cation gets smaller, coordination # drops from 8 to 6, sodium chloride structure; cation size decreases a lot, coordination # reduces from 6 to 4, zinc blende structure

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