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Gases CHAPTER 10 Powerpoint from Melissa Brophy’s website (http://teacherweb.com/TX/McNeilHS/brophy/photo7.aspx) and modified for our class

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**Gases (Chapter 10) Resources and Activities**

Textbook - chapter 10 & ppt file Lab activities (1) Exploring Gas Behavior (with LabQuest Units ) (2) Molar volume of a gas (wet lab) POGIL activities: Ideal gas law Partial Pressure Chemtour videos from W.W. Norton (chapter 6 : ideal gas law; Dalton’s law; molecular speed)

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**Animation on gases to view:**

Independent work - view animations & interactive activities (4 in total) and write summary notes on each. These summaries are to be included in your portfolio

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**Activities and Problem set for chapter 10 (due date_______)**

Complete the chapter 10 packet part (a) Characteristics of Gases ( sample, practice and integrative exercises - show work) and part (b) AP Chemistry Gas Law Practice Do all chapter 10 GIST and Visualizing concepts problems - write out questions and answers & show work. (NB Photocopy of questions is also acceptable) TextBook ch. 10– all sections required for regents (in part), SAT II and AP exams Lab activities: (2) POGILS (2)

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**Measurements on Gases Properties of gases**

Gases uniformly fill any container Gases are easily compressed Gases mix completely with any other gas Gases exert pressure on their surroundings Pressure = Force Area

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**Measurements on Gases Measuring pressure**

The barometer – measures atmospheric pressure Inventor – Evangelista Torricelli (1643)

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Measurements on Gases The manometer – measures confined gas pressure

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**Measurements on Gases Units mm Hg (torr) Kilopascal (kPa) Atmospheres**

760 torr = standard pressure Kilopascal (kPa) kPa = standard pressure Atmospheres 1 atmosphere (atm) = standard pressure STP = 1 atm = 760 torr = 760 mmHg = kPa

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**Measurements on Gases Example: Convert 0.985 atm to torr and to kPa.**

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**The Gas Laws of Boyle, Charles and Avogadro**

Boyle’s Law (Robert Boyle, ) The product of pressure times volume is a constant, provided the temperature remains the same PV = k

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**The Gas Laws of Boyle, Charles and Avogadro**

P is inversely related to V The graph of P versus V is hyperbolic Volume increases linearly as the pressure decreases As you squeeze a zip lock bag filled with air (reducing the volume), the pressure increases making it difficult to keep squeezing

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**The Gas Laws of Boyle, Charles and Avogadro**

At constant temperature, Boyle’s law can be used to find a new volume or a new pressure P1V1 = k = P2V2 or P1V1 = P2V2 Boyle’s law works best at low pressures Gases that obey Boyle’s law are called Ideal gases

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**The Gas Laws of Boyle, Charles and Avogadro**

Example: A gas which has a pressure of 1.3 atm occupies a volume of 27 L. What volume will the gas occupy if the pressure is increased to 3.9 atm at constant temperature? P1 = 1.3 atm V1 = 27 L P2 = 3.9 atm V2 = ? (1.3atm)(27L) = (3.9atm)V2 V2 = 9.0 L

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**The Gas Laws of Boyle, Charles and Avogadro**

Charles’ Law (Jacques Charles, 1746 – 1823) The volume of a gas increase linearly with temperature provided the pressure remains constant V = bT V = b V1 = b = V2 T T T2 or V1 = V2 T T2

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**The Gas Laws of Boyle, Charles and Avogadro**

Temperature must be measured in Kelvin ( K = °C + 273) 0 K is “absolute zero”

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**The Gas Laws of Boyle, Charles and Avogadro**

Example: A gas at 30°C and 1.00 atm has a volume of 0.842L. What volume will the gas occupy at 60°C and 1.00 atm? V1 = 0.842L T1 = 30°C (+273 = 303K) V2 = ? T2 = 60°C (+273 = 333K)

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0.842L = V2 303K K V2 = 0.925L

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**The Gas Laws of Boyle, Charles and Avogadro**

Avogadro’s Law (Amedeo Avogadro, 1811) For a gas at constant temperature and pressure, the volume is directly proportional to the number of moles, n V = an V/n = a V1 = a = V or V1 = V2 n n n n2

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**The Gas Laws of Boyle, Charles and Avogadro**

Example: A 5.20L sample at 18°C and 2.00 atm contains moles of a gas. If we add an additional 1.27 moles of the gas at the same temperature and pressure, what will the total volume occupied by the gas be? V1 = 5.20L n1 = mol V2 = ? n2 = 1.27 mol mol = mol

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**The Gas Laws of Boyle, Charles and Avogadro**

5.20 L = V2 0.436 mol mol x = 20.3L

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**The Ideal Gas Law Derivation from existing laws P V = kba(Tn)**

V=k V=bT V=an P V = kba(Tn)

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**The Ideal Gas Law V = nRT or PV = nRT P**

Constants k, b, a are combined into the universal gas constant (R), V = nRT or PV = nRT P

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**The Ideal Gas Law R = PV using standard numbers will give you R nT STP**

P = 1 atm V = 22.4L n = 1 mol T = 273K Therefore if we solve for R, R = L• atm/mol •K

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The Ideal Gas Law Example: A sample containing moles of a gas at 12°C occupies a volume of 12.9L. What pressure does the gas exert? P = ? V = 12.9L n = mol R = L•atm/mol• K T = = 285K

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**The Ideal Gas Law (P)(12.9L) = (0.614mol)(0.0821 L•atm/mol• K)(285K)**

Hint: Rearrange and re-write (watch out for units in numerator and denominator) P =1.11 atm

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**The Ideal Gas Law Combined Law P1V1 = nR = P2V2 or P1V1 = P2V2**

Solving for new volumes, temperature, or pressure (n remaining constant) Combined Law P1V1 = nR = P2V or P1V1 = P2V2 T T T T2

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The Ideal Gas Law Example: A sample of methane gas at atm and 4.0°C occupies a volume of 7.0L. What volume will the gas occupy if the pressure is increased to 1.52 atm and the temperature increased to 11.0°C? P1 = atm P2 = 1.52 atm V1 = 7.0L V2 = ? T1 = = 277K T2 = = 284K

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The Ideal Gas Law (0.848atm)(7.0L) = (1.52atm)(V2) 277K K V2 = 4.0L

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**Gas Stoichiometry Molar volume Things to remember volume M**

One mole of an ideal gas occupies 22.4L of volume at STP Things to remember Density = mass volume n = grams of substance = m molar mass M PV = mRT M

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Gas Stoichiometry Example: A sample containing 15.0g of dry ice (CO2(s)) is put into a balloon and allowed to sublime according to the following equation: CO2(s) CO2(g) How big will the balloon be (i.e. what is the volume of the balloon) at 22°C and 1.04 atm, after all of the dry ice has sublimed?

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**Gas Stoichiometry Moles of CO2(s): 15g 1 mol = 0.341 mol CO2(s) 44 g**

0.341 mol CO2(s) 1 CO2(g) = mol CO2(g) 1 CO2(s) = n

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**Gas Stoichiometry P = 1.04 atm V = ? n = 0.341 mol**

R = L•atm/mol• K T = 22C = 295K V = 7.94L

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Gas Stoichiometry Limiting Reactant Example: L of H2(g) are reacted with 0.600L of O2(g) at STP according to the equation 2H2(g) + O2(g) 2H2O(g) What volume will the H2O occupy at 1.00 atm and 350°C?

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**Gas Stoichiometry H2: 0.5L 1 mol 2 H2O = 0.0223 mol H2O 22.4L 2 H2**

O2: 0.6L 1 mol 2 H2O = mol H2O 22.4L 1 O2

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Gas Stoichiometry H2: (1 atm)(V) = (0.0223mol)( L•atm/mol• K)(623K) V = 1.14L O2: (1atm)(V) = (0.0536mol)( L•atm/mol• K)(623K) V = 2.74L Limiting reactant and how much volume is produced!

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Gas Stoichiometry Density/Molar Mass example: A gas at 34°C and 1.75 atm has a density of 3.40g/L. Calculate the molar mass of the gas. D = mass = g V L P = 1.75 atm R = L•atm/mol• K V = 1L T = = 307K m = 3.40 g M = x

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**Gas Stoichiometry (1.75atm)(1L) = (3.4g)(0.0821 L•atm/mol• K)(307K)**

M = molar mass M = g/mol

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**Dalton’s Law of Partial Pressures (John Dalton, 1803)**

Statement of law “for a mixture of gases in a container, the total pressure exerted is the sum of the pressures each gas would exert if it were alone” It is the total number of moles of particles that is important, not the identity or composition of the gas particles.

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**Dalton’s Law of Partial Pressures**

Derivation Ptotal = P1 + P2 + P3 … P1 = n1RT P2 = n2RT P3 = n3RT …. V V V Ptotal = n1RT + n2RT + n3RT V V V Ptotal = (n1+n2+n3+…) (RT) V Ptotal = ntotal (RT)

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**Dalton’s Law of Partial Pressures**

Example: Oxygen gas is collected over water at 28C. The total pressure of the sample is 5.5 atm. At 28C, the vapor pressure of water is 1.2 atm. What pressure is the oxygen gas exerting? Ptotal = PO2 + PH2O 5.5 = x + 1.2 X = 4.3 atm

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**Dalton’s Law of Partial Pressures**

Mole Fraction The ratio of the number of moles of a given component in a mixture to the total number of moles in the mixture For an ideal gas, the mole fraction (x): x1 = n = P1 ntotal Ptotal

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**Dalton’s Law of Partial Pressures**

Example: The vapor pressure of water in air at 28°C is 28.3 torr. Calculate the mole fraction of water in a sample of air at 28°C and 1.03 atm. XH2O = PH2O = torr Pair torr = 0.036

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**Dalton’s Law of Partial Pressures**

Example: A mixture of gases contains 1.5 moles of oxygen, 7.5 moles of nitrogen and 0.5 moles of carbon dioxide. If the total pressure exerted is 800 mmHg, what are the partial pressures of each gas in the mixture?

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**Dalton’s Law of Partial Pressures**

Calculate the total number of moles = 9.5 moles Use mole fractions for each individual gas PO2: 800mmHg x 1.5 mol = 126 mmHg 9.5 mol PN2: 800mmHg x 7.5 mol = 632 mmHg PCO2: 800mmHg x 0.5 mol = 42 mmHg

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**Kinetic Molecular Theory of Gases**

Postulates of the KMT Related to Ideal Gases The particles are so small compared with the distances between them that the volume of the individual particles can be assumed to be zero The particles are in constant motion. Collisions of the particles with the walls of the container cause pressure. Assume that the particles exert no forces on each other The average kinetic energy of a collection of gas particles is assumed to be directly proportional to the Kelvin temperature of the gas

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**Kinetic Molecular Theory of Gases**

Explaining Observed Behavior with KMT P and V (T = constant) As V is decreased, P increases: V decrease causes a decrease in the surface area. Since P is force/area, the decrease in V causes the area to decrease, thus increasing the P

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**Kinetic Molecular Theory of Gases**

P and T (V = constant) As T increase, P increases The increase in T causes an increase in average kinetic energy. Molecules moving faster collide with the walls of the container more frequently, and with greater force.

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**Kinetic Molecular Theory of Gases**

V and T (P = constant) As T increases, V also increases Increased T creates more frequent, more forceful collisions. V must increase proportionally to increase the surface area, and maintain P

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**Kinetic Molecular Theory of Gases**

V and n (T and P constant) As n increases, V must increase Increasing the number of particles increases the number of collisions. This can be balanced by an increase in V to maintain constant P

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**Kinetic Molecular Theory of Gases**

Dalton’s Law of partial pressures P is independent of the type of gas molecule KMT states that particles are independent, and V is assumed to be zero. The identity of the molecule is therefore unimportant

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**Kinetic Molecular Theory of Gases**

Root Mean Square Velocity Velocity of a gas is dependent on mass and temperature Velocity of gases is determined as an average M = mass of one mole of gas particles in kg R = J/K•mol joule = kg•m2/s2 urms = 3RT M

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**Kinetic Molecular Theory of Gases**

Example: Calculate the root mean square velocity for the atoms in a sample of oxygen gas at 0°C. MO2 = 32g/mol 32g 1 kg = kg 1000g T = = 273K R = J/K•mol

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**Kinetic Molecular Theory of Gases**

Urms = 3( kg•m2 •s-2•K-1 •mol-1)(273 K) = 461m•s-1 0.032 kg•mol-1 Answer 461m•s-1 or 461 m/s Recall 1 Joule = 1 J = 1 kg• m2/s2 = 1 kg• m2• s-2

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**Kinetic Molecular Theory of Gases**

Mean Free Path – distance between collisions Average distance a molecule travels between collisions 1 x m for O2 at STP

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**Effusion and Diffusion**

Movement of a gas through a small opening into an evacuated container (vacuum) Graham’s law of effusion Rate of effusion for gas 1 = √M2 Rate of effusion for gas 2 √M1

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**Effusion and Diffusion**

Example: How many times faster than He would NO2 gas effuse? MNO2 = g/mol larger mass MHe = g/mol effuses slower Rate He = = He effuses 3.39 Rate NO times faster

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**Real Gases and van der Waals Equation (Johannes van der Waals, 1873)**

Volume Real gas molecules do have volume Volume available is not 100% of the container volume n= number of moles b = is an empirical constant, derived from experimental results

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**Real Gases and van der Waals Equation**

Ideal: P = nRT V Real: P = nRT V-nb

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**Real Gases and van der Waals Equation**

Pressure Molecules of real gases do experience attractive forces a = proportionality constant determined by observation of the gas Pobs = Pideal – a(n/V)2

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**Real Gases and van der Waals Equation**

Combining to derive van der Waals equation Pobs = nRT - n2a V-nb V2 And then rearranging… (Pobs + n2a/V2)(V-nb) = nRT

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**Chemistry in the Atmosphere**

Composition of the Troposphere The atmosphere is composed of 78% N2, 21% O2, 0.9%Ar, and 0.03% CO2 along with trace gases. The composition of the atmosphere varies as a function of distance from the earth’s surface. Heavier molecules tend to be near the surface due to gravity.

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**Chemistry in the Atmosphere**

Upper atmospheric chemistry is largely affected by ultraviolet, x ray, and cosmic radiation emanating from space. The ozone layer is especially reactive to ultraviolet radiation Manufacturing and other processes of our modern society affect the chemistry of our atmosphere. Air pollution is a direct result of such processes.

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Chpt 5 - Gases Gas Law Development Dalton’s Partial pressure law

Chpt 5 - Gases Gas Law Development Dalton’s Partial pressure law

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