10.1 [134 marks] 1. [1 mark] Iron is a stronger reducing agent than silver. What is correct when this voltaic cell is in operation? Markscheme D 2. [1 mark] What is correct in an electrolytic cell? Markscheme D 3. [1 mark] Which functional groups are present in this molecule? A. carbonyl, ether, nitrile B. carbonyl, ester, nitrile C. carboxyl, ether, amine D. carboxyl, ester, amine Markscheme A 4. [1 mark] What is the IUPAC name of this molecule? A. 1,1,2,4-tetramethylpent-1-ene B. 2,4,5-trimethylhex-4-ene C. 2,4,5,5-tetramethylpent-4-ene D. 2,3,5-trimethylhex-2-ene Markscheme D 5. [1 mark] Which compound with the molecular formula πΆ4 π»8 π has this high resolution H1 NMR? From: libretexts.org. Courtesy of Chris Schaller, Professor (Chemistry) at College of Saint Benedict/Saint John’s University. A. but-3-en-2-ol, πΆπ»2 = πΆπ»πΆπ»(ππ»)πΆπ»3 B. butanal, πΆπ»3 πΆπ»2 πΆπ»2 πΆπ»π C. butanone, πΆπ»3 πΆππΆπ»2 πΆπ»3 D. but-3-en-1-ol, πΆπ»2 = πΆπ»πΆπ»2 πΆπ»2 ππ» Markscheme B 6a. [2 marks] Compound A is in equilibrium with compound B. Predict the electron domain and molecular geometries around the oxygen atom of molecule A using VSEPR. Markscheme Electron domain geometry: tetrahedral β Molecular geometry: bent/V-shaped β 6b. [1 mark] The IR spectrum of one of the compounds is shown: COBLENTZ SOCIETY. Collection © 2018 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. Deduce, giving a reason, the compound producing this spectrum. Markscheme B AND πΆ = π absorption/1750 << ππ−1 >> OR B AND absence of ππ» /3200 − 3600 << ππ−1 πππ ππππ‘πππ >> β Accept any value between 1700 − 1750 ππ−1 . 6c. [2 marks] Compound A and B are isomers. Draw two other structural isomers with the formula πΆ3 π»6 π. Markscheme Accept any two πΆ3 π»6 π isomers except for propanone and propen-2-ol: ββ Penalize missing hydrogens in displayed structural formulas once only. 6d. [1 mark] The equilibrium constant, πΎπ , for the conversion of A to B is 1.0 × 108 in water at 298πΎ. Deduce, giving a reason, which compound, A or B, is present in greater concentration when equilibrium is reached. Markscheme π΅ AND πΎπ is greater than 1/large β 7a. [1 mark] Nickel catalyses the conversion of propanone to propan-2-ol. Outline how a catalyst increases the rate of reaction. Markscheme provides an alternative pathway/mechanism AND lower πΈπ β Accept description of how catalyst lowers πΈπ (e.g. “reactants adsorb on surface «of catalyst»”, “reactant bonds weaken «when adsorbed»”). 7b. [2 marks] Explain why an increase in temperature increases the rate of reaction. Markscheme more/greater proportion of molecules with πΈ ≥ πΈπ β greater frequency/probability/chance of collisions «between the molecules» OR more collision per unit of time/second β 7c. [3 marks] Discuss, referring to intermolecular forces present, the relative volatility of propanone and propan-2-ol. Markscheme hydrogen bonding/bonds «and dipole–dipole and London/dispersion forces are present in» propan-2-ol β dipole–dipole «and London/dispersion are present in» propanone β propan-2-ol less volatile AND hydrogen bonding/bonds stronger «than dipole–dipole » OR propan-2-ol less volatile AND «sum of all» intermolecular forces stronger β 7d. [1 mark] The diagram shows an unlabelled voltaic cell for the reaction ππ 2+ (ππ) + ππ(π ) → ππ 2+ (ππ) + ππ(π ) Label the diagram with the species in the equation. Markscheme 7e. [1 mark] Suggest a metal that could replace nickel in a new half-cell and reverse the electron flow. Use section 25 of the data booklet. Markscheme π΅π/πΆπ’/π΄π/ππ/π»π/ππ‘/π΄π’ β Accept ππ OR π΄π . 7f. [2 marks] Describe the bonding in metals. Markscheme electrostatic attraction β between «a lattice of» metal/positive ions/cations AND «a sea of» delocalized electrons β Accept “mobile/free electrons”. 7g. [1 mark] Nickel alloys are used in aircraft gas turbines. Suggest a physical property altered by the addition of another metal to nickel. Markscheme Any of: malleability/hardness OR «tensile» strength/ductility OR density OR thermal/electrical conductivity OR melting point OR thermal expansion β Do not accept corrosion/reactivity or any chemical property. Accept other specific physical properties. 8a. [1 mark] Chlorine undergoes many reactions. State the full electron configuration of the chlorine atom. Markscheme 1π 2 2π 2 2π6 3π 2 3π5 β Do not accept condensed electron configuration. 8b. [1 mark] State, giving a reason, whether the chlorine atom or the chloride ion has a larger radius. Markscheme πΆπ − AND more «electron–electron» repulsion β Accept πΆπ − AND has an extra electron. 8c. [2 marks] Outline why the chlorine atom has a smaller atomic radius than the sulfur atom. Markscheme πΆπ has a greater nuclear charge/number of protons/ππππ «causing a stronger pull on the outer electrons» β same number of shells OR same «outer» energy level OR similar shielding β 8d. [1 mark] The mass spectrum of chlorine is shown. NIST Mass Spectrometry Data Center Collection © 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. Outline the reason for the two peaks at π/π§ = 35 and 37. Markscheme «two major» isotopes «of atomic mass 35 and 37» β 8e. [2 marks] Explain the presence and relative abundance of the peak at π/π§ = 74. Markscheme «diatomic» molecule composed of «two» chlorine-37 atoms β chlorine-37 is the least abundant «isotope» OR low probability of two Cl37 «isotopes» occurring in a molecule β 8f. [1 mark] 2.67π of manganese(IV) oxide was added to 200.0ππ3 of 2.00πππππ−3 π»πΆπ. πππ2 (π ) + 4π»πΆπ(ππ) → πΆπ2 (π) + 2π»2 π(π) + πππΆπ2 (ππ) Calculate the amount, in πππ, of manganese(IV) oxide added. Markscheme 2.67π << 86.94ππππ−1 =>> 0.0307 << πππ >> β 8g. [2 marks] Determine the limiting reactant, showing your calculations. Markscheme << ππ»πΆπ = 2.00πππππ−3 × 0.2000ππ3 >>= 0.400πππ β << 0.400 4 =>> 0.100πππ AND πππ2 is the limiting reactant β Accept other valid methods of determining the limiting reactant in M2. 8h. [1 mark] Determine the excess amount, in πππ, of the other reactant. Markscheme << 0.0307πππ × 4 = 0.123πππ >> << 0.400πππ0.123πππ =>> 0.277 << πππ >> β 8i. [1 mark] Calculate the volume of chlorine, in ππ3 , produced if the reaction is conducted at standard temperature and pressure (STP). Use section 2 of the data booklet. Markscheme << 0.0307πππ × 22.7ππ3 πππ −1 =>> 0.697 << ππ3 >> β Accept methods employing ππ = ππ π. 8j. [2 marks] State the oxidation state of manganese in πππ2 and πππΆπ2 . Markscheme πππ2 : +4 β πππΆπ2 : +2 β 8k. [1 mark] Deduce, referring to oxidation states, whether πππ2 is an oxidizing or reducing agent. Markscheme oxidizing agent AND oxidation state of ππ changes from +4 to +2/decreases β 8l. [1 mark] Chlorine gas reacts with water to produce hypochlorous acid and hydrochloric acid. πΆπ2 (π) + π»2 π(π) β π»πΆππ(ππ) + π»πΆπ(ππ) Hypochlorous acid is considered a weak acid. Outline what is meant by the term weak acid. Markscheme partially dissociates/ionizes «in water» β 8m. [1 mark] State the formula of the conjugate base of hypochlorous acid. Markscheme πΆππ− β 8n. [1 mark] Calculate the concentration of π» + (ππ) in a π»πΆππ(ππ) solution with a ππ» = 3.61. Markscheme << [π» + ] = 10−3.61 =>> 2.5 × 10−4 << πππππ−3 >> β 8o. [1 mark] State the type of reaction occurring when ethane reacts with chlorine to produce chloroethane. Markscheme «free radical» substitution/ππ β Do not accept electrophilic or nucleophilic substitution. 8p. [1 mark] Predict, giving a reason, whether ethane or chloroethane is more reactive. Markscheme chloroethane AND C–Cl bond is weaker/324ππ½πππ −1 than C–H bond/414ππ½πππ −1 OR chloroethane AND contains a polar bond β Accept “chloroethane AND polar”. 8q. [3 marks] Explain the mechanism of the reaction between chloroethane and aqueous sodium hydroxide, ππππ»(ππ), using curly arrows to represent the movement of electron pairs. Markscheme curly arrow going from lone pair/negative charge on π in −OH to πΆ β curly arrow showing πΆπ leaving β representation of transition state showing negative charge, square brackets and partial bonds β Accept ππ» − with or without the lone pair. Do not accept curly arrows originating on π» in ππ» − . Accept curly arrows in the transition state. Do not penalize if π»π and πΆπ are not at 180°. Do not award M3 if ππ» − πΆ bond is represented. 8r. [1 mark] Ethoxyethane (diethyl ether) can be used as a solvent for this conversion. Draw the structural formula of ethoxyethane Markscheme / πΆπ»3 πΆπ»2 ππΆπ»2 πΆπ»3 β Accept (πΆπ»3 πΆπ»2 )2 π. 8s. [3 marks] Deduce the number of signals and chemical shifts with splitting patterns in the 1H NMR spectrum of ethoxyethane. Use section 27 of the data booklet. Markscheme 2 «signals» β 0.9−1.0 AND triplet β 3.3−3.7 AND quartet β Accept any values in the ranges. Award [1] for two correct chemical shifts or two correct splitting patterns. 8t. [2 marks] πΆπΆπ2 πΉ2 is a common chlorofluorocarbon, πΆπΉπΆ. Calculate the percentage by mass of chlorine in πΆπΆπ2 πΉ2. Markscheme << π(πΆπΆπ2 πΉ2 ) =>> 120.91 << ππππ −1 >> β 2×35.45ππππ−1 120.91ππππ−1 × 100% =>> 58.64 << % >> β Award [2] for correct final answer. 8u. [1 mark] Comment on how international cooperation has contributed to the lowering of πΆπΉπΆ emissions responsible for ozone depletion. Markscheme Any of: research «collaboration» for alternative technologies «to replace πΆπΉπΆs» OR technologies «developed»/data could be shared OR political pressure/Montreal Protocol/governments passing legislations β Do not accept just “collaboration”. Do not accept any reference to πΆπΉπΆ as greenhouse gas or product of fossil fuel combustion. Accept reference to specific measures, such as agreement on banning use/manufacture of πΆπΉπΆs. 8v. [2 marks] πΆπΉπΆs produce chlorine radicals. Write two successive propagation steps to show how chlorine radicals catalyse the depletion of ozone. Markscheme π3 + πΆπ → π2 + πΆππ β πΆππ + π → π2 + πΆπ OR πΆππ + π3 → πΆπ + 2π2 β Penalize missing/incorrect radical dot (β) once only. 9a. [2 marks] Predict the electron domain and molecular geometries around the oxygen atom of molecule A using VSEPR Markscheme Electron domain geometry: tetrahedral β Molecular geometry: bent/V-shaped β 9b. [1 mark] State the type of hybridization shown by the central carbon atom in molecule B. Markscheme π π2 β 9c. [1 mark] State the number of sigma (π) and pi (π) bonds around the central carbon atom in molecule B. Markscheme π-bonds: 3 AND π-bonds: 1 β 9d. [1 mark] The IR spectrum of one of the compounds is shown: COBLENTZ SOCIETY. Collection © 2018 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. Deduce, giving a reason, the compound producing this spectrum. Markscheme B AND πΆ = π absorption/1750 << ππ−1 >> OR B AND absence of ππ» /3200 − 3600 << ππ−1 πππ ππππ‘πππ >> β Accept any value between 1700 − 1750 ππ−1 . 9e. [2 marks] Compound A and B are isomers. Draw two other structural isomers with the formula πΆ3 π»6 π. Markscheme Accept any two πΆ3 π»6 π isomers except for propanone and propen-2-ol: ββ Penalize missing hydrogens in displayed structural formulas once only. 9f. [1 mark] The equilibrium constant, πΎπ , for the conversion of A to B is 1.0 × 108 in water at 298πΎ. Deduce, giving a reason, which compound, A or B, is present in greater concentration when equilibrium is reached. Markscheme π΅ AND πΎπ is greater than 1/large β 9g. [1 mark] Calculate the standard Gibbs free energy change, πΊ , in π€ππ¦π¨π₯1 , for the reaction (A to B) at 298πΎ. Use sections 1 and 2 of the data booklet. Markscheme << π₯πΊ π© = −π πlnπΎ = 0.00831ππ½πππ −1 πΎ −1 (298πΎ) (ln 1.0 × 108 ) =>> −46 << ππ½πππ −1 >> β 9h. [3 marks] Propanone can be synthesized in two steps from propene. Suggest the synthetic route including all the necessary reactants and steps. Markscheme π»2 π/water «and π» + » β πΆπ»3 πΆπ»(ππ»)πΆπ»3/propan-2-ol β πΎ2 πΆπ2 π7/«potassium» dichromate(VI) AND π» + OR πΎπππ4 /«acidified potassium» manganate(VII) β Accept π»3 π + . 9i. [2 marks] Propanone can be synthesized in two steps from propene. Suggest why propanal is a minor product obtained from the synthetic route in (g)(i). Markscheme primary carbocation «intermediate forms» OR minor product «of the water addition would be» propan-1-ol OR anti-Markovnikov addition of water β primary alcohol/propan-1-ol oxidizes to an aldehyde/propanal β 10a. [1 mark] Outline how a catalyst increases the rate of reaction. Markscheme provides an alternative pathway/mechanism AND lower Ea β Accept description of how catalyst lowers Ea (e.g. “reactants adsorb on surface «of catalyst»”, “reactant bonds weaken «when adsorbed»”). 10b. [2 marks] Explain why an increase in temperature increases the rate of reaction. Markscheme more/greater proportion of molecules with E Ea β greater frequency/probability/chance of collisions «between the molecules» OR more collision per unit of time/second β 10c. [3 marks] Discuss, referring to intermolecular forces present, the relative volatility of propanone and propan-2-ol. Markscheme hydrogen bonding/bonds «and dipole–dipole and London/dispersion forces are present in» propan-2-ol β dipole–dipole «and London/dispersion are present in» propanone β propan-2-ol less volatile AND hydrogen bonding/bonds stronger «than dipole–dipole » OR propan-2-ol less volatile AND «sum of all» intermolecular forces stronger β 10d. [1 mark] The diagram shows an unlabelled voltaic cell for the reaction ππ 2+ (ππ) + ππ(π ) → ππ 2+ (ππ) + ππ(π ) Label the diagram with the species in the equation. Markscheme 10e. [1 mark] Calculate the standard cell potential, in π, for the cell at 298πΎ. Use section 24 of the data booklet Markscheme << −0.13π − (−0.26π) = +>> 0.13 << π >> β 10f. [1 mark] Calculate the standard free energy change, πΊ , in π€π, for the cell using sections 1 and 2 of the data booklet. Markscheme << π₯πΊ π© = −ππΉπΈ π© = −2 × 96500 × 0.13 1000 =>> −25 << ππ½ >> β 10g. [1 mark] Suggest a metal that could replace nickel in a new half-cell and reverse the electron flow. Use section 25 of the data booklet. Markscheme π΅π/πΆπ’/π΄π/ππ/π»π/ππ‘/π΄π’ β Accept ππ OR π΄π . 10h. [2 marks] Describe the bonding in metals. Markscheme electrostatic attraction β between «a lattice of» metal/positive ions/cations AND «a sea of» delocalized electrons β Accept “mobile/free electrons”. 10i. [1 mark] Nickel alloys are used in aircraft gas turbines. Suggest a physical property altered by the addition of another metal to nickel. Markscheme Any of: malleability/hardness OR «tensile» strength/ductility OR density OR thermal/electrical conductivity OR melting point OR thermal expansion β Do not accept corrosion/reactivity or any chemical property. Accept other specific physical properties. 11a. [2 marks] Consider the structures of medicinal molecules in section 37 of the data booklet. Name two functional groups that both zanamivir and oseltamivir contain. Markscheme Any two: «secondary» carboxamide/amido β ether β carbonyl β Accept amide Accept amino/amine. Accept alkenyl/alkene. Do not accept formula. 11b. [2 marks] Explain how zanamivir works as a preventative agent against flu viruses. Markscheme «drug» blocks/inhibits «viral» enzyme/neuraminidase/ππ΄ «activity» β prevents virus from leaving/escaping host cells «thus cannot infect other cells» β Do not accept other anti-viral methods (as question is specific to Zanamivir). 11c. [1 mark] Circle the side-chain in penicillin on the structure below. Markscheme β Accept a circle that does not surround the amido group. Do not accept a circle that only surrounds the phenol group. 11d. [2 marks] Explain, with reference to the action of penicillin, why new penicillins with different sidechains need to be produced. Markscheme bacterial resistance «to older penicillins/antibiotics» β prevent penicillinase/beta-lactamase/enzyme in bacterium to deactivate/open penicillin/beta-lactam ring β Accept “antibiotic resistant bacteria” but not “antibiotic resistance” for M1. Accept “reduce allergic reactions from from penicillin” for M2. Award [1 max] for “increased efficiency” OR “increased stability in GIT”. Do not accept “bacteria develop tolerance”. 11e. [2 marks] State and explain the relative solubility of codeine in water compared to morphine and diamorphine. Markscheme codeine less soluble «in water» than morphine AND more soluble than diamorphine OR morphine > codeine > diamorphine «in terms of solubility in water» β more/stronger/greater hydrogen/H bonding «due to more hydroxyl groups leads to greater solubility» β 11f. [1 mark] State the natural source from which codeine, morphine and diamorphine are obtained. Markscheme opium poppy/plants/seeds β Accept “poppy” OR “opioid”. 12a. [2 marks] There has been significant growth in the use of carbon nanotubes, CNT. Explain these properties of carbon nanotubes. Markscheme Excellent strength: defect-free AND rigid/regular 2D/3D β Excellent conductivity: delocalized electrons β Accept “carbons/atoms are all covalently bonded to each other” for M1. 12b. [1 mark] Alloying metals changes their properties. Suggest one property of magnesium that could be improved by making a magnesium–CNT alloy. Markscheme Any of: ductility β strength/resistance to deformation β malleability β hardness β resistance to corrosion/chemical resistance β range of working temperatures β density β Do not accept “conductivity”. 12c. [2 marks] Pure magnesium needed for making alloys can be obtained by electrolysis of molten magnesium chloride. © International Baccalaureate Organization 2020. Write the half-equations for the reactions occurring in this electrolysis. Markscheme Anode: 2πΆπ − → πΆπ2 (π) + 2π − β Cathode: ππ2+ + 2π − → ππ(π) β Accept πΆπ − → πΆπ2 (π) + π . Award [1 max] for correct equations at incorrect electrodes. 12d. [3 marks] Calculate the theoretical mass of magnesium obtained if a current of 3.00π΄ is used for 10.0 hours. Use charge (π) = ππ’πππππ‘(πΌ) × π‘πππ(π‘) and section 2 of the data booklet Markscheme << π = πΌ × π‘ = 3.00 × 10.0 × 3600 =>> 108000πΆ β << π πΉ 108000πΆ = 96500πΆπππ −1 =>> 1.12 << πππ π − >> β 1.12πππ = 0.560πππππ >> 2 << π = 0.560πππ × 24.31ππππ −1 =>> 13.6 << π >> β << Award [3] for correct final answer. 12e. [1 mark] Suggest a gas which should be continuously passed over the molten magnesium in the electrolytic cell. Markscheme argon/π΄π/helium/π»π β Accept any identified noble/inert gas. Accept name OR formula. Do not accept “nitrogen/π2 “. 12f. [1 mark] Zeolites can be used as catalysts in the manufacture of CNT. Explain, with reference to their structure, the high selectivity of zeolites. Markscheme pores/cavities/channels/holes/cage-like structures β «only» reactants with appropriate/specific size/geometry/structure fit inside/go through/are activated/can react β Accept “molecules/ions” for “reactants” in M2. 12g. [1 mark] Experiments have been done to explore the nematic liquid crystal behaviour of CNT. Justify how CNT molecules could be classified as nematic. Markscheme rod-shaped molecules OR «randomly distributed but» generally align OR no positional order AND have «some» directional order/pattern β Accept “linear” for “rod-shaped”. 13a. [1 mark] Gasoline (petrol), biodiesel and ethanol are fuels. [U.S. Department of Energy. https://afdc.energy.gov/] Calculate the energy released, in ππ½, from the complete combustion of 5.00ππ3 of ethanol. Markscheme << 21200ππ½ππ−3 × 5.00ππ3 =>> 106000/1.06 × 105 << ππ½ >> β 13b. [1 mark] State a class of organic compounds found in gasoline. Markscheme alkane OR cycloalkane OR arene β Accept “alkene”. Do not accept just “hydrocarbon”, since given in stem. Do not accept “benzene/aromatic” for “arene”. 13c. [4 marks] Outline the advantages and disadvantages of using biodiesel instead of gasoline as fuel for a car. Exclude any discussion of cost. Markscheme Advantages: [2 max] renewable β uses up waste «such as used cooking oil» β lower carbon footprint/carbon neutral β higher flashpoint β produces less πππ₯ /ππ2 OR less polluting emissions β has lubricating properties OR preserves/increases lifespan of engine β increases the life of the catalytic converter β eliminates dependence on foreign suppliers β does not require pipelines/infrastructure «to produce» β relatively less destruction of habitat compared to obtaining petrochemicals β Accept “higher energy density” OR “biodegradable” for advantage. Disadvantages: [2 max] needs conversion/transesterification β takes time to produce/grow plants β takes up land OR deforestation β fertilizers/pesticides/phosphates/nitrates «used in production of crops» have negative environmental effects β biodiversity affected OR loss of habitats «due to energy crop plantations» β cannot be used at low temperatures β variable quality «in production» β high viscosity/can clog/damage engines β Accept “lower specific energy” as disadvantage. Do not accept “lower octane number” as disadvantage”. 13d. [1 mark] A mixture of gasoline and ethanol is often used as a fuel. Suggest an advantage of such a mixture over the use of pure gasoline. Exclude any discussion of cost. Markscheme Any one: uses up fossil fuels more slowly β lower carbon footprint/CO2 emissions β undergoes more complete combustion β produces fewer particulates β higher octane number/rating OR less knocking β prevents fuel injection system build up OR helps keep engine clean β Accept an example of a suitable advantage even if repeated from 9c. 13e. [2 marks] Contrast the molecular structures of biodiesel and the vegetable oil from which it is formed. Markscheme Any two: biodiesel has smaller molecules/single «hydrocarbon» chain AND oil has larger molecules/multiple «hydrocarbon» chains β biodiesel is methyl/ethyl ester AND oil has «backbone of» glycerol joined to fatty acids β biodiesel contains one ester group AND oil contains three ester groups β Do not accept properties such as “less viscous” or “lower ignition point”. 13f. [1 mark] When combusted, all three fuels can release carbon dioxide, a greenhouse gas, as well as particulates. Contrast how carbon dioxide and particulates interact with sunlight. Markscheme carbon dioxide allows sunlight/short wavelength radiation to pass through AND particulates reflect/scatter/absorb sunlight β Accept “particulates reflect/scatter/absorb sunlight AND carbon dioxide does not”. Accept “πΆπ2 absorbs πΌπ «radiation» AND particulates reflect/scatter/absorb sunlight”. Do not accept “traps” for “absorbs”. 13g. [2 marks] Methane is another greenhouse gas. Contrast the reasons why methane and carbon dioxide are considered significant greenhouse gases. Markscheme carbon dioxide is highly/more abundant «in the atmosphere» β methane is more effective/potent «as a greenhouse gas» OR methane/better/more effective at absorbing πΌπ «radiation» OR methane has greater greenhouse factor OR methane has greater global warming potential/GWPβ Accept “carbon dioxide contributes more to global warming” for M1. 13h. [1 mark] Suggest a wavenumber absorbed by methane gas. Markscheme any value or range within 28503090 << ππ−1 >> β 14a. [1 mark] Calculate the energy released, in ππ½, from the complete combustion of 5.00ππ3 of ethanol. Markscheme << 21200ππ½ππ−3 × 5.00ππ3 =>> 106000/1.06 × 105 << ππ½ >> β 14b. [1 mark] State a class of organic compounds found in gasoline. Markscheme alkane OR cycloalkane OR arene β Accept “alkene”. Do not accept just “hydrocarbon”, since given in stem. Do not accept “benzene/aromatic” for “arene”. 14c. [4 marks] Outline the advantages and disadvantages of using biodiesel instead of gasoline as fuel for a car. Exclude any discussion of cost. Markscheme Advantages: [2 max] renewable β uses up waste «such as used cooking oil» β lower carbon footprint/carbon neutral β higher flashpoint β produces less πππ₯ /ππ2 OR less polluting emissions β has lubricating properties OR preserves/increases lifespan of engine β increases the life of the catalytic converter β eliminates dependence on foreign suppliers β does not require pipelines/infrastructure «to produce» β relatively less destruction of habitat compared to obtaining petrochemicals β Accept “higher energy density” OR “biodegradable” for advantage. Disadvantages: [2 max] needs conversion/transesterification β takes time to produce/grow plants β takes up land OR deforestation β fertilizers/pesticides/phosphates/nitrates «used in production of crops» have negative environmental effects β biodiversity affected OR loss of habitats «due to energy crop plantations» β cannot be used at low temperatures β variable quality «in production» β high viscosity/can clog/damage engines β Accept “lower specific energy” as disadvantage. Do not accept “lower octane number” as disadvantage”. 14d. [1 mark] A mixture of gasoline and ethanol is often used as a fuel. Suggest an advantage of such a mixture over the use of pure gasoline. Exclude any discussion of cost. Markscheme Any one: uses up fossil fuels more slowly β lower carbon footprint/CO2 emissions β undergoes more complete combustion β produces fewer particulates β higher octane number/rating OR less knocking β prevents fuel injection system build up OR helps keep engine clean β Accept an example of a suitable advantage even if repeated from 11c. 14e. [1 mark] When combusted, all three fuels can release carbon dioxide, a greenhouse gas, as well as particulates. Contrast how carbon dioxide and particulates interact with sunlight. Markscheme carbon dioxide allows sunlight/short wavelength radiation to pass through AND particulates reflect/scatter/absorb sunlight β Accept “particulates reflect/scatter/absorb sunlight AND carbon dioxide does not”. Accept “πΆπ2 absorbs πΌπ «radiation» AND particulates reflect/scatter/absorb sunlight”. Do not accept “traps” for “absorbs”. 14f. [2 marks] Methane is another greenhouse gas. Contrast the reasons why methane and carbon dioxide are considered significant greenhouse gases. Markscheme carbon dioxide is highly/more abundant «in the atmosphere» β methane is more effective/potent «as a greenhouse gas» OR methane/better/more effective at absorbing πΌπ «radiation» OR methane has greater greenhouse factor OR methane has greater global warming potential/GWPβ Accept “carbon dioxide contributes more to global warming” for M1. 14g. [1 mark] Suggest a wavenumber absorbed by methane gas. Markscheme any value or range within 28503090 << ππ−1 >> β 14h. [1 mark] Determine the relative rate of effusion of methane (ππ = 16.05) to carbon dioxide (ππ = 44.01), under the same conditions of temperature and pressure. Use section 1 of the data booklet. Markscheme πΆπ» 44.01 «rate of effusion of πΆπ4 = √16.05 =>> 1.656 β 2 15. [1 mark] What is formed at the electrodes during the electrolysis of molten sodium bromide? Markscheme D 16. [1 mark] Which compound is not in the same homologous series as the others? A. C5H12 B. C6H12 C. C7H16 D. C8H18 Markscheme B 17. [1 mark] Where does oxidation occur in a voltaic cell? A. positive electrode and anode B. negative electrode and anode C. positive electrode and cathode D. negative electrode and cathode Markscheme B 18. [1 mark] Which product will be obtained at the anode (positive electrode) when molten NaCl is electrolysed? A. Na (l) B. Cl (g) C. Cl2 (g) D. Na (s) Markscheme C 19. [1 mark] Which functional group is surrounded in the molecule? A. hydroxyl B. carboxyl C. carbonyl D. ether Markscheme C 20. [1 mark] What is the IUPAC name of the following molecule? A. 2-bromo-3-ethylbutane B. 3-methyl-4-bromopentane C. 2-ethyl-3-bromobutane D. 2-bromo-3-methylpentane Markscheme D 21. [1 mark] Consider the following electrochemical cell. What happens to the ions in the salt bridge when a current flows? A. Na+ ions flow to the zinc half-cell and SO42− ions flow to the copper half-cell. B. Na+ ions flow to the copper half-cell and SO42− ions flow to the zinc half-cell. C. Na+ and SO42− ions flow to the copper half-cell. D. Na+ and SO42− ions flow to the zinc half-cell. Markscheme B Printed for GREEN HILLS ACAD SEC © International Baccalaureate Organization 2021 International Baccalaureate® - Baccalauréat International® - Bachillerato Internacional®