Gases. States of Matter. Molecular Arrangement Solid Small Small Ordered Liquid Unity Unity Local Order Gas High Large Chaotic (random)



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Gases States of Matter States of Matter Kinetic E (motion) Potential E(interaction) Distance Between (size) Molecular Arrangement Solid Small Small Ordered Liquid Unity Unity Local Order Gas High Large Chaotic (random) (http://www.chem.neu.edu/courses/1105tom/05lecture19_files/image002.jpg Individual Molecules in Gas Gas is made of molecules in motion can be pure He or CH 4 etc. or mixture of molecules Air contains Ar, CO 2, O 2, H 2 O, N 2 Gas Properties and Ideal Gas Law Pressure p (atm) Volume V (L) Temperature T (K) Moles n (mol) Gas Constant R (0.08206 L atm/mol K) Ideal Gas Law p V = n R T links properties together Always use Kelvin temperature scale in pv = nrt o C = ( o F 32)/1.8 K = o C + 273.15 Atmospheric Pressure Measured with a Barometer Pressure = Force/ Area

Height of column of Mercury (Hg) is way to measure pressure. Mercury can expand with temperature but effect is small in wide bore column. Careful measurements correct for temperature expansion. Pressure units used: 1.01 x 10 5 Pa = 1.01 bar = 760 mm Hg =760 torr = 1 atm = 14.7 lbs/in 2 psi Note:Pa = Pascal (N/m 2 ) and bar is 10 5 Pa Atmospheric Pressure Measured with a Barometer Ex: Miami 760 mm Hg Denver 628 mm Hg Chattanooga 740 mm Hg (http://theory.uwinnipeg.ca/physics/fluids/node9.html) Difference in Pressure with a Manometer

(http://www.dwyer-inst.com/htdocs/pressure/manometerintroduction.cfm) High pressure can be measured with metal diaphragm Development of Ideal Gas Law 1660 Boyle s Law V α 1/P 1703 Amonton s Law P α T (Gay-Lussac) P= (const) (T)

1787 Charles Law V α T V= (const) ( T) 1811 Avogadro Law V α n Equal number of molecules in equal volumes Summarize Ideal Gas Law V ~ (1/P) (T) (n) V = R (1/P) (T) (n) (http://dwb.unl.edu/teacher/nsf/c09/c09content.html) p V = n R T where R is gas constant Absolute Zero Charles Law introduces idea of lowest possible temperature V is proportional to T and plotting data for helium gas shows that V = 0 at T= -273 o C which we call Absolute Zero T = -273.15 o C (Celsius) = 0 K (zero Kelvin) Standard Temperature and Pressure (STP) At T = 0 o C = 273 K and P = 1 atm = 760 mmhg

1 mole occupies 22.4 L 6.02 x 10 23 molecules occupy 22.4L at STP but have different densities O 2 32 g/mol 1.43 g/l Ar 40 g/mol 1.79 g/l CH 4 16 g/mol 0.72 g/l Different weight but the same mass Density = w/v (g/l) or (g/cm 3 ) V, P, T moles use V, P, T to determine the # of moles Molecular Weight M = w/ n (weight / moles) Gas Constant R pv = nrt Ideal Gas Law where R= gas constant R= pv/nt R= (22.414 L) (1.000 atm)/ (1.000 mol) ( 273.15 K) R = 0.08206 L atm/ K mol or R= (2.21 x 10-2 m 3 ) ( 1.01 x 10 5 Pa) / (273.15 K) (1 mol) R= 8.31 m 3 Pa / K mol and Pa = (N / m 2 ) x m 3 = N x m = J so R= 8.31 J/ K mol Values of R will be given on exams Use R= 0.08206 L atm/ K mol for gas law problems trying to find amounts of P, V, or T Use R= 8.31 J/ K mol for calculations trying to find energy Problems using Gas Law a. Direct Substitution b. Change c. Stoichiometry

a. Direct Substitution 1. Write down what you know p = 320 mm Hg (329)( 1atm/ 760) = 0.421 atm T = 27 o C 300 K N = ½ mol 0.5 mol R = 0.08206 L atm mol K V =? 2. Convert to proper units 3. Find Symbolic Solution (rearrange pv=nrt for what you are seeking) pv = nrt V =? V= nrt/ P 4. Substitute in Numbers and do math V = (0.5 mol)( 0.08206 L atm/ mol K)( 300 K) = 29.2 L (0.421 atm) b. Change 1. Write Before 2. Write After (fix units if needed) P 1 = 1 atm P 2 =? V 1 = 2.0 L V 2 = 6.0 L T 1 = 200 K T 2 = 400 K 3. Find Symbolic P 1 V 1 / n T 1 = P 2 V 2 / n T 2 Cross out any property that is constant P 2 = (V 1 / V 2 ) ( T 2 / T 1 ) P 1 4. Substitute in Numbers and do math P 2 = (2.0L/6.0L) (400K/200K) (1 atm) = 0.67 atm

c. Stoichiometry 1. Do regular stoichiometry problem 2. Do gas law problem with answer from part 1 Ex. Water is converted to gas by electrolysis. Starting with 100g H 2 O produces what volume of H 2, O 2, at STP? 2H 2 O (l) 2H 2 (g) + O 2 (g) 100g x (1.00 mol / 18.0g) = 5.56 mol H 2 O 5.56 x (2/2) = 5.56 mol H 2 5.56 x (1/2) = 2.78 mol O 2 at STP 22.4 L/ mol so 125 L H 2 and 62.5 L O 2 from pv = nrt V =? V = (nrt/ p) = (2.78 mol)(0.08206 L atm / mol K)( 273 K )=62.3L (1 atm) Partial Pressure Based on Mixture of Gases that don t react chemically Ex. Air is mixture of N 2, O 2, CO 2, Ar, H 2 O Total Pressure of the mixture is the sum of the components P TOTAL = P A + P B + P C P TOTAL = P N2 + P O2 + P CO2 + P Ar + P H2O = 5.75 + 134 + 12 + 4 + 20 =745 mm Hg in general for gases A, B, and C for gases in air Keep track of relative number of molecules Mole fraction X A X A = (n A / n TOTAL ) = (n A ) / (n A + n B + n C +...)

Sum of the mole fractions (components) is one 1 = X A + X B + X C +... To calculate partial pressure from mole fraction Can use ideal gas law with partial pressure as do for pressure Volume is total volume of container p A V = n A RT p B V = n B RT etc. p A = Pressure of A n A = Moles of A Molecular Speed Higher temperature Higher speed Higher kinetic energy Typical room temperature values Speed ~ 180 m/s ~ 400 mph Collisions ~ 10 10 collisions/second (collisions are random) Diffusion is much slower than molecular speed Distance between collisions ~ 10-7 m Speeds of molecules is greater for lighter molecules and greater at higher temperatures http://en.wikipedia.org/wiki/image:maxwellboltzmann.gif#file Kinetic Molecular Theory of Gases Explain behavior of gases in terms of molecule assumptions:

1. Size of gas molecules is negligible (molecules small compared distances between) 2. Attractive forces between molecules are negligible 3. Molecules are in constant random motion, collide with each other and walls 4. Kinetic energy proportional to temperature Ideal gas law NOT followed At high pressure size important, molecules packed together At low temperature interactions become important There are other equations of state more complicated Science observations Law Model Results of Kinetic Molecular Theory pv = nrt pressure depends on number of collisions per area p increases if... V decreases T increases n increases small volume, less wall area more collisions each a collision has more energy more molecules more collisions Mathematical Derivation of Ideal Gas Law from Kinetic Theory We will not cover these math details and you are not responsible for -(discussed in some GChem textbooks) Average Molecular Speed Ex. What is the average speed of nitrogen gas molecules? 3/2 ( RT ) = 1/2 (Mu 2 ) where M = molar mass u avg = ( 3RT/M ) 1/2

= ( 3 (8.31 J/mol K) (300K) ) / (0.028 kg/mol) ) 1/2 = 517 m/s since (J/kg) 1/2 = (m 2 / s 2 ) 1/2 = 517 m/s ( mi/1609 m)( 3600s/ hr) = 517 mi/s (2.24) = 1160 mph! Effusion The movement of molecules through hole is effusion Movement of molecules through gas or liquid is diffusion In general relative rate of effusion is given by: Rate A / Rate B = (M B /M A ) where M = mass Ex. Comparison of rate of He to N 2 He faster than N 2 since mass less

Rate He/ Rate N 2 = 2.65 = (M N2 / M He ) = ( 28/4) = 2.65 Can use to determine molar mass of one gas relative to known gas Real Gases Kinetic Molecular Theory for Ideal Gas must be modified to account for real gas behavior 1. Gas Molecules do have interactions attractions for each other (collisions are sticky) 2. Gas Molecules do have volume can only be compressed so far can not be squeezed together too close Van der Waals Equation of State includes parameters that relate to size and interactions P = ( nrt / ( V nb) ) (a n 2 / V 2 ) P is less due to attractions of molecules Weaker interactions between molecules mean lower temperatures required to convert from gas to liquid (at 1 atm, the normal boiling point) He bp = 4K and N 2 bp = 77 K Therefore N 2 has stronger interactions than He Generally larger molecules have stronger interactions but water is unusual because small molecule with high boiling point H 2 O bp = 373 K dipole Extra Stoichiometry Problem Ex. 50g of CaCO 3 heated produces what volume of CO 2 at STP? CaCO 3 (s) heat CaO(s) + CO 2 (g)?mol CaCO 3 = 50g CaCO 3 (mol/ 100 g) = 0.50molCaCO 3 and CO 2 is same moles as CaCO3 therefore use 0.50 mole of CO 2 PV=nRT V = nrt/p V = (0.50mol)(.08206 L atm/mol K) (273K)/(1.00atm) = 11.2 L

Extra Problem to find Molar Mass Find the molecular weight of CO 2 from observing the mass of CO 2 produced and the volume it occupies. Experiment CaCO 3 (s) + heat CaO (s) + CO 2 (g) CO 2 (g) collected at 1.00 atm and 300 K and mass or of CO 2 was 11g And volume of CO 2 was 6.15 L 1) Convert volume to moles pv = nrt n = pv/rt = (1 atm)( 6.15 L) = 0.25 mol (0.08206 L atm/mol K)(300K) 2) Calculate the molecular weight W (molar mass) of CO 2 and use Density = m/v in (g/cm 3 ) or (g/l) Heavier the molecule the larger the density W = m / n (g/mol) W = 11g / 0.25 mol = 44 g/mol for CO 2 Example Gas Density Calculation Density d = m/v Moles of Gas n = m/w m = mass (g) W = molecular weight (g /mol) n = pv/ RT Combining above gives n = m/w = pv/ RT And simplifying m/v = pw/rt d density = m/v = pw/ RT

Example for NO 2 d= [(1 atm)( 46 g/mol)] / [(0.08206 L atm/ mol K)(273 K) ] = 2.05 g/l Note that liquid densities are measured in g/ml and gas densities in g/l so about a factor of 1000 different. Gases are much less dense than liquids.