M09/4/CHEMI/SP2/ENG/TZ1/XX+ CHEMISTRY. Monday 18 May 2009 (afternoon) Candidate session number. 1 hour 15 minutes INSTRUCTIONS TO CANDIDATES

Similar documents
M10/4/CHEMI/SP2/ENG/TZ1/XX+ CHEMISTRY. Wednesday 12 May 2010 (afternoon) Candidate session number. 1 hour 15 minutes INSTRUCTIONS TO CANDIDATES

M09/4/CHEMI/SP2/ENG/TZ2/XX CHEMISTRY. Monday 18 May 2009 (afternoon) Candidate session number. 1 hour 15 minutes INSTRUCTIONS TO CANDIDATES

M08/4/CHEMI/SP2/ENG/TZ2/XX CHEMISTRY. Thursday 8 May 2008 (afternoon) Candidate session number. 1 hour 15 minutes INSTRUCTIONS TO CANDIDATES

1. What is the sum of all coefficients when the following equation is balanced using the smallest possible whole numbers? D.

N10/4/CHEMI/SP2/ENG/TZ0/XX CHEMISTRY STANDARD LEVEL PAPER 2. Thursday 11 November 2010 (afternoon) Candidate session number.

T2-1P1 [187 marks] [1 mark] How many protons, neutrons and electrons are present in each atom of 31 P? [1 mark]

List, with an explanation, the three compounds in order of increasing carbon to oxygen bond length (shortest first).

Alcohols. Ethanol Production. 182 minutes. 181 marks. Page 1 of 25

Cherry Hill Tuition A Level Chemistry OCR (A) Paper 12

CHEMISTRY Unit 2 Energy, Rate and Chemistry of Carbon Compounds

T8-1P1 [212 marks] [1 mark] Which is an acid-base conjugate pair? A. H3 O / OH B. H2SO 4 / SO4 C. CH3COOH / H3 O D. CH3NH 3 + / CH3NH2.

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

3.2.9 Alkenes. Addition Reactions. 271 minutes. 268 marks. Page 1 of 35

CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certificate of Education Advanced Subsidiary Level and Advanced Level

Thursday 19 January 2012 Afternoon

A.M. MONDAY, 7 June hours

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

Candidate Name Centre Number Candidate Number. Energy, Rate and Chemistry of Carbon Compounds

PAPER 2 MAY/JUNE SESSION hour

3.2.1 Energetics. Enthalpy Change. 263 minutes. 259 marks. Page 1 of 41

Cherry Hill Tuition A Level Chemistry OCR (A) Paper 9 THIS IS A NEW SPECIFICATION

CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certificate of Education Advanced Subsidiary Level and Advanced Level

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

Wednesday 23 May 2012 Afternoon

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

Chemistry *P45044A0128* Pearson Edexcel P45044A

N09/4/CHEMI/HP2/ENG/TZ0/XX+ CHEMISTRY HIGHER level. Tuesday 3 November 2009 (afternoon) Candidate session number. 2 hours 15 minutes

(2) (1) (2) The isotopic composition of a sample of sulphur is found using a mass spectrometer.

B410U10-1 S16-B410U10-1. CHEMISTRY Component 1 The Language of Chemistry, Structure of Matter and Simple Reactions

Unit 4: General Principles of Chemistry I Rates, Equilibria and Further Organic Chemistry (including synoptic assessment)

Cherry Hill Tuition A Level Chemistry OCR (A) Paper 10 THIS IS A NEW SPECIFICATION

AQA Chemistry Checklist

Questions Q1. The first ionization energies, in kj mol -1, of four elements with consecutive atomic numbers are shown below. A 1680 B 2080 C 496 D 738

alkane molecular formula boiling point / C H 6 H 8 H [1] Explain why the boiling points increase down the alkane homologous series....

Edexcel Chemistry Checklist

Cherry Hill Tuition A Level Chemistry OCR (A) Paper 11

Chemistry *P40135A0116* P40135A. Unit: KCH0/4CH0 Paper: 2C. Edexcel Certificate Edexcel International GCSE. Tuesday 29 May 2012 Morning Time: 1 hour

PhysicsAndMathsTutor.com. Advanced Subsidiary Paper 2: Core Organic and Physical Chemistry

Lower Sixth Chemistry. Sample Entrance Examination

3.2.6 Group II. Trends in Chemical properties. 164 minutes. 161 marks. Page 1 of 19

Chemistry *P42992A0128* Pearson Edexcel P42992A

F322: Chains, Energy and Resources Basic Concepts

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

Friday 10 June 2016 Afternoon Time allowed: 1 hour 30 minutes

International Advanced Level Chemistry Advanced Subsidiary Unit 2: Application of Core Principles of Chemistry

Q1. Which one of the following is not a correct general formula for the non-cyclic compounds listed?

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

A-level CHEMISTRY CHEM4. Unit 4 Kinetics, Equilibria and Organic Chemistry. Afternoon. (JUN16CHEM401) WMP/Jun16/E5. Materials.

CHEMISTRY. Section II (Total time 95 minutes) Part A Time 55 minutes YOU MAY USE YOUR CALCULATOR FOR PART A.

Wednesday 16 January 2013 Morning

B410U20-1 S17-B410U20-1. CHEMISTRY AS component 2 Energy, Rate and Chemistry of Carbon Compounds

Candidate number. Centre number

A-level CHEMISTRY 7405/1. Paper 1: Inorganic and Physical Chemistry. SPECIMEN MATERIAL v1.2

THIS IS A NEW SPECIFICATION

1 The structures of six organic compounds are shown. H H H H H H H C C C H H H H H O H D E F. (a) Give the name of F. ... [1]

2 Answer all the questions. 1 Born Haber cycles can be used to calculate enthalpy changes indirectly.

London Examinations GCE

1 hour 30 minutes plus your additional time allowance

PHYSICAL SCIENCES/ P2 1 SEPTEMBER 2015 CAPS CAPE WINELANDS EDUCATION DISTRICT

SPECIMEN. Date Morning/Afternoon Time allowed: 1 hour 30 minutes. AS Level Chemistry A H032/01 Breadth in chemistry Sample Question Paper PMT

Propanone can be formed when glucose comes into contact with bacteria in the absence of air. Deduce the role of the bacteria in this reaction.

AS CHEMISTRY 7404/2. Paper 2: Organic and Physical Chemistry

Q1. (a) Explain the meaning of the terms mean bond enthalpy and standard enthalpy of formation. Mean bond enthalpy

*P51939A0124* Pearson Edexcel WCH04/01. P51939A 2018 Pearson Education Ltd.

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED SUBSIDIARY GCE F322 CHEMISTRY A. Chains, Energy and Resources

... [1] Draw another structural isomer of these two alcohols.

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

CHEM5. General Certificate of Education Advanced Level Examination June Unit 5 Energetics, Redox and Inorganic Chemistry

AS Level Chemistry B (Salters) H033/01 Foundations of chemistry Date Morning/Afternoon You must have: You may use: First name Last name

Chemistry Assessment Unit AS 1

CHEMISTRY HIGHER LEVEL

Unit 3(a) Introduction to Organic Chemistry

Advanced Subsidiary Unit 1: The Core Principles of Chemistry. Wednesday 11 January 2017 Morning Time: 1 hour 30 minutes

Coimisiún na Scrúduithe Stáit State Examinations Commission

2 Examiner SECTION A. Answer all the questions in the spaces provided.

M14/4/CHEMI/SPM/ENG/TZ1/XX CHEMISTRY. Monday 19 May 2014 (afternoon) 45 minutes INSTRUCTIONS TO CANDIDATES

Q1. Methane and oxygen react together to produce carbon dioxide and water.

Chapter 10 Organic Reactions

CHEM1. General Certificate of Education Advanced Subsidiary Examination June Unit 1 Foundation Chemistry. Monday 23 May pm to 2.

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certificate of Education Advanced Subsidiary Level and Advanced Level

B410U10-1 S17-B410U10-1. CHEMISTRY AS component 1 The Language of Chemistry, Structure of Matter and Simple Reactions

T3-2P3 [51 marks] Bromine is a member of group 7, the halogens. [3 marks] Explain the trend in reactivity of the halogens. 1a.

CHEM1. General Certificate of Education Advanced Subsidiary Examination June Foundation Chemistry. (JUN09CHEM101) APW/Jun09/CHEM1 TOTAL

Chemistry Assessment Unit A2 1

CHEM2. General Certificate of Education Advanced Subsidiary Examination January Unit 2 Chemistry in Action

(03) WMP/Jun10/CHEM4

London Examinations IGCSE

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

CHEM1. General Certificate of Education Advanced Subsidiary Examination January Unit 1 Foundation Chemistry

Carbon and its Compounds

Advanced Subsidiary Unit 1: The Core Principles of Chemistry

London Examinations IGCSE

3.2.1 Energetics. Calorimetry. 121 minutes. 120 marks. Page 1 of 19

International School of Johannesburg. Diploma Chemistry. Organic Chemistry (HL) Revision Questions. D. ( HNCH 2 CH 2 NHCOCH 2 NH ) (Total 1 mark)

A-level CHEMISTRY (7405/1)

Transcription:

M09/4/EMI/SP2/ENG/TZ1/XX+ 22096111 EMISTRY standard level Paper 2 Monday 18 May 2009 (afternoon) 1 hour 15 minutes 0 0 andidate session number INSTRUTINS T ANDIDATES Write your session number in the boxes above. Do not open this examination paper until instructed to do so. Section A: answer all of Section A in the spaces provided. Section B: answer one question from Section B. Write your answers on answer sheets. Write your session number on each answer sheet, and attach them to this examination paper and your cover sheet using the tag provided. At the end of the examination, indicate the numbers of the questions answered in the candidate box on your cover sheet and indicate the number of sheets used in the appropriate box on your cover sheet. 13 pages International Baccalaureate rganization 2009 0113

Answer all the questions in the spaces provided. 2 M09/4/EMI/SP2/ENG/TZ1/XX+ Section a 1. Biodiesel makes use of plants ability to fix atmospheric carbon by photosynthesis. Many companies and individuals are now using biodiesel as a fuel in order to reduce their carbon footprint. Biodiesel can be synthesized from vegetable oil according to the following reaction. R R R Na (s) (l) + 3 3 (l) (l) + 3 3 R (l) vegetable oil methanol glycerol biodiesel (a) Identify the organic functional group present in both vegetable oil and biodiesel. For part of her extended essay investigation into the efficiency of the process, a student reacted a pure sample of a vegetable oil (where R = 17 33 ) with methanol. The raw data recorded for the reaction is below. Mass of oil = 1013.0 g Mass of methanol = 200.0 g Mass of sodium hydroxide = 3.5 g Mass of biodiesel produced = 811.0 g The relative molecular mass of the oil used by the student is 885.6. alculate the amount (in moles) of the oil and the methanol used, and hence the amount (in moles) of excess methanol. [3] (This question continues on the following page) 0213

3 M09/4/EMI/SP2/ENG/TZ1/XX+ (Question 1 continued) (c) The reversible arrows in the equation indicate that the production of biodiesel is an equilibrium process. (i) State what is meant by the term dynamic equilibrium. Using the abbreviations [vegetable oil], [methanol], [glycerol] and [biodiesel] deduce the equilibrium constant expression (K c ) for this reaction. (iii) Suggest a reason why excess methanol is used in this process. (iv) State and explain the effect that the addition of the sodium hydroxide catalyst will have on the position of equilibrium. (d) The reactants had to be stirred vigorously because they formed two distinct layers in the reaction vessel. Explain why they form two distinct layers and why stirring increases the rate of reaction. (This question continues on the following page) 0313 Turn over

4 M09/4/EMI/SP2/ENG/TZ1/XX+ (Question 1 continued) (e) (f) alculate the percentage yield of biodiesel obtained in this process. When biodiesel is combusted it produces carbon dioxide. Explain why the use of biodiesel as a fuel does not significantly contribute to global warming. 0413

5 M09/4/EMI/SP2/ENG/TZ1/XX+ Blank page 0513 Turn over

6 M09/4/EMI/SP2/ENG/TZ1/XX+ 2. Two students were asked to use information from the Data Booklet to calculate a value for the enthalpy of hydrogenation of ethene to form ethane. (g) 2 4 + (g) 2 (g) 2 6 John used the average bond enthalpies from Table 10. Marit used the values of enthalpies of combustion from Table 12. (a) alculate the value for the enthalpy of hydrogenation of ethene obtained using the average bond enthalpies given in Table 10. Marit arranged the values she found in Table 12 into an energy cycle. ë Ö (hydrogenation) 2 4 (g) + 2 (g) 2 6 (g) 3 2 1411 kj mol 1 1 2 2 286 kj mol 1 3 1 2 2 1560 kj mol 1 2 2 (g) + 3 2 (l) alculate the value for the enthalpy of hydrogenation of ethene from the energy cycle. (c) Suggest one reason why John s answer is slightly less accurate than Marit s answer. (This question continues on the following page) 0613

7 M09/4/EMI/SP2/ENG/TZ1/XX+ (Question 2 continued) (d) John then decided to determine the enthalpy of hydrogenation of cyclohexene to produce cyclohexane. (i) () l + ( g) () l 6 10 2 6 12 Use the average bond enthalpies to deduce a value for the enthalpy of hydrogenation of cyclohexene. The percentage difference between these two methods (average bond enthalpies and enthalpies of combustion) is greater for cyclohexene than it was for ethene. John s hypothesis was that it would be the same. Determine why the use of average bond enthalpies is less accurate for the cyclohexene equation shown above, than it was for ethene. Deduce what extra information is needed to provide a more accurate answer. 0713 Turn over

3. Sodium oxide, Na 2, is a white solid with a high melting point. 8 M09/4/EMI/SP2/ENG/TZ1/XX+ (a) Explain why solid sodium oxide is a non-conductor of electricity. Molten sodium oxide is a good conductor of electricity. State the half-equation for the reaction occurring at the positive electrode during the electrolysis of molten sodium oxide. (c) (i) State the acid-base nature of sodium oxide. State the equation for the reaction of sodium oxide with water. 0813

9 4. (a) Define oxidation in terms of electron transfer. M09/4/EMI/SP2/ENG/TZ1/XX+ hlorine can be made by reacting concentrated hydrochloric acid with potassium manganate(vii), KMn 4. 2KMn 4(aq) + 16l(aq) 2Mnl 2(aq) + 2Kl(aq) + 5l 2(aq) + 82(aq) (i) State the oxidation number of manganese in KMn 4 and in Mnl 2. KMn 4... Mnl 2........................................................ Deduce which species has been oxidized in this reaction and state the change in oxidation number that it has undergone. 0913 Turn over

10 M09/4/EMI/SP2/ENG/TZ1/XX+ Section b Answer one question. Write your answers on the answer sheets provided. Write your session number on each answer sheet, and attach them to this examination paper and your cover sheet using the tag provided. 5. (a) (i) Describe and explain the operation of a mass spectrometer. [5] State three factors that affect the degree of deflection of ions in a mass spectrometer. [3] (iii) Strontium exists as four naturally-occurring isotopes. alculate the relative atomic mass of strontium to two decimal places from the following data. Isotope Percentage abundance Sr-84 0.56 Sr-86 9.90 Sr-87 7.00 Sr-88 82.54 (This question continues on the following page) 1013

11 M09/4/EMI/SP2/ENG/TZ1/XX+ (Question 5 continued) The graph of the first ionization energy plotted against atomic number for the first twenty elements shows periodicity. 2500 2000 First ionization energy / kj mol 1 1500 1000 500 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 Atomic number (i) Define the term first ionization energy and state what is meant by the term periodicity. State the electron arrangement of argon and explain why the noble gases, helium, neon and argon show the highest first ionization energies for their respective periods. [3] (iii) A graph of atomic radius plotted against atomic number shows that the atomic radius decreases across a period. Explain why chlorine has a smaller atomic radius than sodium. (iv) Explain why a sulfide ion, S 2, is larger than a chloride ion, l. (v) Explain why the melting points of the Group 1 metals ( Li s) decrease down the group whereas the melting points of the Group 7 elements ( F I) increase down the group. [3] 1113 Turn over

12 M09/4/EMI/SP2/ENG/TZ1/XX+ 6. (a) (i) Draw the Lewis structures for carbon monoxide,, carbon dioxide, 2 and methanol, 3. [3] List, with an explanation, the three compounds in order of increasing carbon to oxygen bond length (shortest first). Predict the shape and bond angles for the following species: (i) 2 3 2 (iii) BF 4 (c) (i) Define a Brønsted-Lowry acid. Deduce the two acids and their conjugate bases in the following reaction: + (l) + N(aq) (aq) + N (aq) 2 3 4 (iii) Explain why the following reaction can also be described as an acid-base reaction. F(g) + BF (g) BF (s) 3 4 (d) Ethanoic acid, 3, is a weak acid. (i) Define the term weak acid and state the equation for the reaction of ethanoic acid with water. Vinegar, which contains ethanoic acid, can be used to clean deposits of calcium carbonate from the elements of electric kettles. State the equation for the reaction of ethanoic acid with calcium carbonate. 1213

13 M09/4/EMI/SP2/ENG/TZ1/XX+ 7. (a) Three compounds with similar relative molecular masses are butane, propanal and propan-1-ol. (i) List the three compounds in order of increasing boiling point (lowest first) and explain the differences in their boiling points. [4] Predict, with an explanation, which of the three compounds is least soluble or miscible in water. (iii) When propan-1-ol is oxidized using a warm acidified solution of potassium dichromate(vi) two different organic products can be obtained. Deduce the name and structural formula for each of these two products. [3] (iv) Propan-2-ol is an isomer of propan-1-ol. Draw the structure of propan-2-ol. (v) Identify the class of alcohols that propan-2-ol belongs to and state the name of the organic product formed when it is oxidized by an acidified solution of potassium dichromate(vi). Ethanol can be formed from ethene in a two step reaction: Br step 1 step 2 (g) (g) (l) (i) State the name of the reagent used for step 1. State the name of the reagent and the conditions used for step 2. (iii) The mechanism involved in step 2 is S N 2. Explain how the reaction proceeds using curly arrows to represent the movement of electron pairs. [3] (iv) utline how ethanol is manufactured from ethene in industry and state one important commercial use of ethanol. 1313