University College Chemistry Semester 2 Final Review Study Guide

Comprehensive Overview of Semester 2 College Chemistry Final Review

The final examination consists of 30 multiple-choice questions spanning five major units: Unit 6 (Intermolecular Forces and Properties), Unit 7 (Gases), Unit 8 (Matter and Energy), Unit 9 (Stoichiometry), and Unit 10 (Reactions). Permitted materials during the exam include a regular periodic table, a periodic table of ions, a molecular geometry chart, a stoichiometry map, and a scientific calculator. All necessary equations will be provided on the exam. A specific review of previous problems confirms that while a periodic table of ions (polyatomic ions) is provided, it is not strictly required for questions like the stoichiometry of H2SH_2S (S=32.06gmol1S = 32.06\,g\,mol^{-1}), as standard periodic tables provide necessary molar masses.

Unit 6: Intermolecular Forces and Molecular Properties

Intermolecular forces (IMFs) are determined by the polarity and structure of covalent molecules. For ammonia (NH3NH_3), the molecule is polar and exhibits London Dispersion Forces (LDFs), Dipole-Dipole interactions, and Hydrogen bonding. Methane (CH4CH_4) is non-polar and only possesses LDFs. Hydrogen sulfide (H2SH_2S) is polar with LDFs and Dipole-Dipole interactions. Methanol (CH3OHCH_3OH) is polar and demonstrates LDFs, Dipole-Dipole, and Hydrogen bonding. Ethene (C2H4C_2H_4) is non-polar with only LDFs. Trifluoromethane (CHF3CHF_3) is polar, exhibiting LDFs and Dipole-Dipole forces, but specifically lacks Hydrogen bonding because the Hydrogen is not bonded directly to Nitrogen, Oxygen, or Fluorine.

Boiling point predictions are based on the strength of these IMFs. Methanol (CH3OHCH_3OH) is predicted to have the highest boiling point among these examples because it can Hydrogen bond and has a larger molecular size than NH3NH_3. Furthermore, Oxygen is more electronegative than Nitrogen, making the OHO-H bond more polar. Conversely, ethene (C2H4C_2H_4) is predicted to have the lowest boiling point because it only possesses weak LDFs. In a comparison between CH4CH_4, CF4CF_4, CH3FCH_3F, O2O_2, and NH3NH_3, NH3NH_3 has the highest boiling point due to Hydrogen bonding.

Bond polarity is ranked by the difference in electronegativity (ΔEN\Delta EN). For the bonds SHS-H, CBrC-Br, FNF-N, and OHO-H, the calculated differences are ΔEN=0.4\Delta EN = 0.4 for SHS-H (2.62.22.6 - 2.2), ΔEN=0.4\Delta EN = 0.4 for CBrC-Br (3.02.63.0 - 2.6), ΔEN=1.0\Delta EN = 1.0 for FNF-N (4.03.04.0 - 3.0), and ΔEN=1.5\Delta EN = 1.5 for OHO-H (3.41.93.4 - 1.9). Therefore, the bonds ranked from least polar to most polar are SHS-H and CBrC-Br (tie), followed by FNF-N, and finally OHO-H.

Unit 7: Kinetic Molecular Theory and Gas Laws

A gas exerts pressure on the walls of its container due to the force of collisions of the gas particles with the container walls. Several gas laws describe the relationship between pressure (PP), volume (VV), and temperature (TT). Boyle's Law states that as Volume increases, Pressure decreases; mathematically, this is an inverse relationship where P=1VP = \frac{1}{V} or P1V1=P2V2P_1V_1 = P_2V_2. Charles's Law states that as Temperature increases, Volume increases; this is a direct relationship where V=TV = T or V1T1=V2T2\frac{V_1}{T_1} = \frac{V_2}{T_2}. Gay-Lussac's Law states that as Temperature increases, Pressure increases; this is a direct relationship where P=TP = T or P1T1=P2T2\frac{P_1}{T_1} = \frac{P_2}{T_2}. If the volume of a gas is decreased at a constant temperature, its pressure will increase.

Dalton's Law of Partial Pressure describes the pressure of individual gases in a mixture. The total pressure is the sum of partial pressures (Ptotal=P1+P2+...+PnP_{total} = P_1 + P_2 + ... + P_n). For a mixture of 4.3mol4.3\,mol Argon, 2.8molCO22.8\,mol\,CO_2, and 6.2molN26.2\,mol\,N_2 with a total pressure of 8.7atm8.7\,atm, the total moles are 13.3mol13.3\,mol. The partial pressures are calculated as PAr=4.313.3×8.7=2.8atmP_{Ar} = \frac{4.3}{13.3} \times 8.7 = 2.8\,atm, PCO2=2.813.3×8.7=1.8atmP_{CO_2} = \frac{2.8}{13.3} \times 8.7 = 1.8\,atm, and PN2=6.213.3×8.7=4.1atmP_{N_2} = \frac{6.2}{13.3} \times 8.7 = 4.1\,atm. In another example with a total pressure of 833torr833\,torr, the mole fractions (XiX_i) for N2N_2 (204torr204\,torr), NeNe (172torr172\,torr), and H2H_2 (457torr457\,torr) are XN2=0.245X_{N_2} = 0.245, XNe=0.206X_{Ne} = 0.206, and XH2=0.549X_{H_2} = 0.549.

The Ideal Gas Law is defined as PV=nRTPV = nRT. For a gas with 6.82mol6.82\,mol, a volume of 53.5L53.5\,L, and a pressure of 2.65atm2.65\,atm, using R=0.0821Latmmol1K1R = 0.0821\,L \cdot atm \cdot mol^{-1} \cdot K^{-1}, the temperature is calculated as T=2.65×53.56.82×0.0821=253KT = \frac{2.65 \times 53.5}{6.82 \times 0.0821} = 253\,K. For 8.73moles8.73\,moles of Helium at 344kPa344\,kPa and 58.1C58.1^{\circ}C (331.1K331.1\,K), using R=8.31LkPamol1K1R = 8.31\,L \cdot kPa \cdot mol^{-1} \cdot K^{-1}, the volume is V=8.73×8.31×331.1344=69.8LV = \frac{8.73 \times 8.31 \times 331.1}{344} = 69.8\,L. The Combined Gas Law (P1V1T1=P2V2T2\frac{P_1V_1}{T_1} = \frac{P_2V_2}{T_2}) is used for changing conditions. A balloon with 5.25L5.25\,L at 136kPa136\,kPa and 28.2C28.2^{\circ}C (301.2K301.2\,K) moved to a pressure of 189kPa189\,kPa and 17.3C17.3^{\circ}C (290.3K290.3\,K) will have a new volume of V2=136×5.25×290.3301.2×189=3.64LV_2 = \frac{136 \times 5.25 \times 290.3}{301.2 \times 189} = 3.64\,L.

Unit 8: Matter and Energy

Phase properties distinguish solids, liquids, and gases. Solids have a definite volume and a definite shape, with no space between particles and no translational motion. Liquids have a definite volume but no definite shape; they also lack significant space between particles and translational motion. Gases have no definite volume or shape, are compressible, have significant space between particles, and exhibit translational motion.

Definitions of energy include: Heat, which is the total energy due to particle movement, and Temperature, which is the average kinetic energy of a substance. During a phase change, the potential energy changes while temperature remains constant. Chemical bonds and intermolecular forces are considered forms of potential energy. Specific heat represents the kinetic energy change for 1g1\,g of a substance per 1C1^{\circ}C. Calculations for heat transfer use q=mcΔTq = mc\Delta T, where cc for gaseous water is 1.84Jg1C11.84\,J \cdot g^{-1} \cdot ^{\circ}C^{-1} or 2.08Jg1C12.08\,J \cdot g^{-1} \cdot ^{\circ}C^{-1} depending on the reference used. For 15.0g15.0\,g of water going from Ti=150.8CT_i = 150.8^{\circ}C to Tf=105.9CT_f = 105.9^{\circ}C, the heat transfer is q=15.0×1.84×(105.9150.8)=1239Jq = 15.0 \times 1.84 \times (105.9 - 150.8) = -1239\,J.

Phase changes require enthalpy of fusion (ΔHfus\Delta H_{fus}) or vaporization (ΔHvap\Delta H_{vap}). Calculating the energy to condense 156g156\,g of gaseous water (H2OH_2O) to liquid involves ΔHvap=40.67kJmol1\Delta H_{vap} = 40.67\,kJ\,mol^{-1}. The calculation is ΔH=156g×1mol18.02g×(40.67kJ)=352kJ\Delta H = 156\,g \times \frac{1\,mol}{18.02\,g} \times (-40.67\,kJ) = -352\,kJ. Melting 150.0g150.0\,g of ice (ΔHfus=6.01kJmol1\Delta H_{fus} = 6.01\,kJ\,mol^{-1}) requires ΔH=150.0g×1mol18.02g×6.01kJ=50.0kJ\Delta H = 150.0\,g \times \frac{1\,mol}{18.02\,g} \times 6.01\,kJ = 50.0\,kJ. Calorimetry calculation for enthalpy of solution (ΔHsoln\Delta H_{soln}) uses ΔHsoln=mtotal4.18(TfTi)\Delta H_{soln} = -m_{total} \cdot 4.18 \cdot (T_f - T_i). For example, adding 10g10\,g of CaCl2CaCl_2 to 100g100\,g of H2OH_2O (Ti=24.5CT_i = 24.5^{\circ}C, Tf=39.4CT_f = 39.4^{\circ}C) results in ΔHsoln=110×4.18×(39.424.5)=6851J\Delta H_{soln} = -110 \times 4.18 \times (39.4 - 24.5) = -6851\,J, which is an exothermic process.

Unit 9: Stoichiometry and Yields

Stoichiometry requires balanced chemical equations to determine relationships between reactants and products. In the reaction 2Al(s)+6HCl(aq)2AlCl3(aq)+3H2(g)2\,Al(s) + 6\,HCl(aq) \rightarrow 2\,AlCl_{3}(aq) + 3\,H_{2}(g), reacting 5.2molAl5.2\,mol\,Al requires 15.6molHCl15.6\,mol\,HCl (5.2×625.2 \times \frac{6}{2}). Reacting 7.5molHCl7.5\,mol\,HCl produces 3.75molH23.75\,mol\,H_2 (7.5×367.5 \times \frac{3}{6}). Making 3.25molAlCl33.25\,mol\,AlCl_3 requires the reaction of 3.25molAl3.25\,mol\,Al (3.25×223.25 \times \frac{2}{2}). At STP (Standard Temperature and Pressure), 1mol1\,mol of any gas occupies 22.4L22.4\,L. For the reaction 2H2S(l)+3O2(g)2SO2(g)+2H2O(l)2\,H_2S(l) + 3\,O_2(g) \rightarrow 2\,SO_2(g) + 2\,H_2O(l), reacting 103.5gH2S103.5\,g\,H_2S requires 102LO2102\,L\,O_2 calculated as: 103.5g×1mol34.08g×3O22H2S×22.4L=102L103.5\,g \times \frac{1\,mol}{34.08\,g} \times \frac{3\,O_2}{2\,H_2S} \times 22.4\,L = 102\,L.

Limiting reactants determine the theoretical yield. If 175gCuCl2175\,g\,CuCl_2 reacts with 35.1gAl35.1\,g\,Al in the reaction 2Al+3CuCl22AlCl3+3Cu2\,Al + 3\,CuCl_2 \rightarrow 2\,AlCl_3 + 3\,Cu, the conversion from CuCl2CuCl_2 yields 0.868molAlCl30.868\,mol\,AlCl_3 (116g116\,g), while AlAl yields 1.30molAlCl31.30\,mol\,AlCl_3. Thus, CuCl2CuCl_2 is the limiting reactant and the theoretical yield is 116g116\,g. Percent yield is defined as Actual YieldTheoretical Yield×100\frac{\text{Actual Yield}}{\text{Theoretical Yield}} \times 100. If 4.28LH24.28\,L\,H_2 is actually produced from a theoretical yield of 5.04L5.04\,L, the percent yield is 84.9%84.9\%. In another reaction producing 8.07gNaOH8.07\,g\,NaOH from a theoretical 12.9g12.9\,g, the percent yield is 62.6%62.6\%. For magnesium chloride reacting with sodium (2Na+MgCl22NaCl+Mg2\,Na + MgCl_{2} \rightarrow 2\,NaCl + Mg), reacting 0.255L0.255\,L of 1.75MMgCl21.75\,M\,MgCl_2 requires 20.5gNa20.5\,g\,Na calculated as: 0.255L×1.75molL1×2Na1MgCl2×22.99gmol1=20.5g0.255\,L \times 1.75\,mol\,L^{-1} \times \frac{2\,Na}{1\,MgCl_2} \times 22.99\,g\,mol^{-1} = 20.5\,g.

Unit 10: Chemical Reactions, Kinetics, and Equilibrium

Collision theory states that for a reaction to occur, a collision must have two things: the Activation Energy (EaE_a) and the proper orientation. Five factors affect the rate of reaction: temperature, surface area of solids, concentration of reactants, catalysts, and the pressure of gaseous reactants. Increasing the concentration of products has no effect on the forward reaction rate. Enthalpy of reaction (ΔH\Delta H) is the energy difference between reactants and products. In an energy profile, activation energy (EaE_a) is the energy needed to start bond breaking.

Energy changes can be calculated from bond enthalpies using ΔH=bonds brokenbonds formed\Delta H = \text{bonds broken} - \text{bonds formed}. For the reaction N2H4+O2N2+2H2ON_2H_4 + O_2 \rightarrow N_2 + 2\,H_2O, given bonds NN=163N-N = 163, NH=391N-H = 391, O=O=495O=O = 495, NN=941N \equiv N = 941, and OH=463kJmol1O-H = 463\,kJ\,mol^{-1}, the calculation is ΔH=(163+4×391+495)(941+4×463)=571kJ\Delta H = (163 + 4 \times 391 + 495) - (941 + 4 \times 463) = -571\,kJ. Since ΔH\Delta H is negative, the reaction is exothermic. For the combustion of methane (CH4+2O2CO2+2H2OCH_4 + 2\,O_2 \rightarrow CO_2 + 2\,H_2O), given CH=413C-H = 413, O=O=495O=O = 495, C=O=799C=O = 799, and OH=463kJmol1O-H = 463\,kJ\,mol^{-1}, ΔH=(4×413+2×495)(2×799+4×463)=808kJ\Delta H = (4 \times 413 + 2 \times 495) - (2 \times 799 + 4 \times 463) = -808\,kJ.

Equilibrium is described by the equilibrium constant (KcK_c or KpK_p). For the reaction C(s)+2H2(g)CH4(g)C(s) + 2\,H_2(g) \rightleftharpoons CH_4(g), the expressions are Kc=[CH4][H2]2K_c = \frac{[CH_4]}{[H_2]^2} and Kp=PCH4PH22K_p = \frac{P_{CH_4}}{P_{H_2}^2}, noting that solids like Carbon are excluded. If Kp=0.277K_p = 0.277 and PH2=1.21atmP_{H_2} = 1.21\,atm, then PCH4=1.212×0.277=0.406atmP_{CH_4} = 1.21^2 \times 0.277 = 0.406\,atm. If an equilibrium constant KeqK_{eq} is much less than 1 (e.g., 0.0010.001), the equilibrium mixture contains mostly reactants. Le Chatelier's Principle predicts reaction shifts: for 2SO2(g)+O2(g)2SO3(g)+heat2\,SO_2(g) + O_2(g) \rightleftharpoons 2\,SO_3(g) + \text{heat} (ΔH=39kJ\Delta H = 39\,kJ - wait, if heat is a product, it is exothermic, but the transcript notes ΔH=39kJ\Delta H = 39\,kJ. Based on the provided answer key: adding SO2SO_2 shifts right, removing SO2SO_2 shifts left, adding O2O_2 shifts right, decreasing pressure shifts left, and increasing temperature shifts left for exothermic reactions).

Questions & Discussion

Question: Does any question from the beginning need to use the periodic table of ions?

Answer: Looking back at the questions we have done, no, you do not need a periodic table of ions (polyatomic ions) to solve them. For example, in Question 3 (Stoichiometry), you only needed a regular periodic table to find the molar mass of H2SH_2S (S=32.06gmol1S = 32.06\,g\,mol^{-1}).

Question: Why does a gas exert pressure on the walls of its container?

Answer: The force of the collisions of the gas particles with the container walls creates the pressure.

Question: What are the two things a collision must have in order to produce a reaction?

Answer: It must have sufficient Activation Energy (EaE_a) and the proper orientation.

Question: What is the temperature of 15.0g15.0\,g of water moving between 150.8C150.8^{\circ}C and 105.9C105.9^{\circ}C?

Answer (from ChatGPT margin note): The water is in a gaseous state because the temperature is above 100C100^{\circ}C. Use the formula q=mcΔTq = mc\Delta T. Calculation: 15.0g×1.84Jg1C1×(105.9150.8)=1239J15.0\,g \times 1.84\,J \cdot g^{-1} \cdot ^{\circ}C^{-1} \times (105.9 - 150.8) = -1239\,J.