Thursday 19 January 2012 Afternoon

Similar documents
Analyse this information to suggest possible structures for compounds F, G and H.

Wednesday 23 May 2012 Afternoon

Wednesday 16 January 2013 Morning

Tuesday 2 June 2015 Afternoon

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

Wednesday 16 January 2013 Morning

CHEMISTRY 2812/01 Chains and Rings

Thursday 26 January 2012 Afternoon

Friday 10 June 2016 Afternoon

THIS IS A NEW SPECIFICATION

Tuesday 4 June 2013 Afternoon

CHEMISTRY 2814/01 Chains, Rings and Spectroscopy

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

Chemistry Unit Two (F322) Chains, Energy and Resources

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

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

surname number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED SUBSIDIARY GCE F322 CHEMISTRY A Chains, Energy and Resources

THIS IS A NEW SPECIFICATION

Cherry Hill Tuition A Level Chemistry OCR (A) Paper 1 THIS IS A NEW SPECIFICATION

THIS IS A NEW SPECIFICATION

Candidate number. Centre number

Friday 26 May 2017 Morning

Thursday 10 January 2013 Morning

THIS IS A NEW SPECIFICATION

Thursday 23 May 2013 Morning

THIS IS A NEW SPECIFICATION

A Level Chemistry A H432/02 Synthesis and analytical techniques. Practice paper Set 1 Time allowed: 2 hours 15 minutes

Friday 27 May 2016 Morning

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED SUBSIDIARY GCE F321 CHEMISTRY A. Atoms, Bonds and Groups

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

Tuesday 19 June 2012 Afternoon

Monday 19 June 2017 Morning Time allowed: 2 hours 15 minutes

Thursday 10 January 2013 Morning

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED SUBSIDIARY GCE F332/TEST CHEMISTRY B (SALTERS) Chemistry of Natural Resources

F321. CHEMISTRY A Atoms, Bonds and Groups ADVANCED SUBSIDIARY GCE. Thursday 13 January 2011 Morning PMT. Duration: 1 hour

Candidate number. Centre number

Tuesday 14 June 2016 Afternoon

Wednesday 19 June 2013 Morning

F334. CHEMISTRY B (SALTERS) Chemistry of Materials ADVANCED GCE. Friday 24 June 2011 Morning. Duration: 1 hour 30 minutes

Tuesday 22 January 2013 Afternoon

CHEMISTRY 2814/01 Chains, Rings and Spectroscopy

Monday 19 June 2017 Morning

F331. CHEMISTRY B (SALTERS) Chemistry for Life ADVANCED SUBSIDIARY GCE. Monday 23 May 2011 Afternoon. Duration: 1 hour 15 minutes

Wednesday 16 January 2013 Morning

F331. CHEMISTRY B (SALTERS) Chemistry for Life ADVANCED SUBSIDIARY GCE. Thursday 13 January 2011 Morning. Duration: 1 hour 15 minutes

CHEMISTRY Chains and Rings. OXFORD CAMBRIDGE AND RSA EXAMINATIONS Advanced Subsidiary GCE

Monday 14 January 2013 Afternoon

CHEMISTRY 2815/01 Trends and Patterns

Thursday 19 January 2012 Afternoon

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

F324. CHEMISTRY A Rings, Polymers and Analysis ADVANCED GCE. Friday 24 June 2011 Morning PMT. Duration: 1 hour

Tuesday 4 June 2013 Afternoon

Tuesday 13 June 2017 Afternoon

THIS IS A NEW SPECIFICATION MODIFIED LANGUAGE

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

Wednesday 13 June 2012 Morning

F332/TEST. CHEMISTRY B (SALTERS) Chemistry of Natural Resources ADVANCED SUBSIDIARY GCE. Friday 27 May 2011 Afternoon. Duration: 1 hour 45 minutes

CHEMISTRY 2816/01 Unifying Concepts in Chemistry

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED SUBSIDIARY GCE F332/TEST CHEMISTRY B (SALTERS) Chemistry of Natural Resources

Afternoon Time: 1 hour 30 minutes

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED GCE F324 CHEMISTRY A. Rings, Polymers and Analysis

THIS IS A NEW SPECIFICATION

THIS IS A NEW SPECIFICATION MODIFIED LANGUAGE

THIS IS A NEW SPECIFICATION

CHEMISTRY 2811/01 Foundation Chemistry

Tuesday 2 June 2015 Afternoon

surname number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED GCE F324 CHEMISTRY A Rings, Polymers and Analysis

surname number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED SUBSIDIARY GCE F322 CHEMISTRY A Chains, Energy and Resources

F322: Chains, Energy and Resources Basic Concepts

G484. PHYSICS A The Newtonian World ADVANCED GCE. Thursday 27 January 2011 Afternoon. Duration: 1 hour

SPECIMEN. Date Morning/Afternoon Time allowed: 1 hour 30 minutes. AS Level Chemistry B (Salters) H033/02 Chemistry in depth Sample Question Paper

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED GCE F325 CHEMISTRY A. Equilibria, Energetics and Elements

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED SUBSIDIARY GCE F331 CHEMISTRY B (SALTERS) Chemistry for Life

Tuesday 14 June 2016 Afternoon

Surname. Number OXFORD CAMBRIDGE AND RSA EXAMINATIONS ADVANCED GCE F324 CHEMISTRY A. Rings, Polymers and Analysis

CHEMISTRY Unit 2 Energy, Rate and Chemistry of Carbon Compounds

GCSE (9 1) Chemistry A (Gateway Science) J248/04 Paper 4, C4 C6 and C7 (Higher Tier)

Wednesday 1 February 2012 Morning

A Level Chemistry A H432/01 Periodic table, elements and physical chemistry. Practice paper - Set 1 Time allowed: 2 hours 15 minutes

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

Compound A [1]... have different boiling points.

This document consists of 16 printed pages and a Data Sheet for Chemistry.

Wednesday 21 May 2014 Afternoon

THIS IS A NEW SPECIFICATION

Morning. This document consists of 15 printed pages, 1 blank page and a Data Sheet for Chemistry.

Candidate number. Centre number

Candidate number. Centre number

Date Morning/Afternoon Time allowed: 1 hour 30 minutes

Wednesday 22 June 2016 Morning

Wednesday 1 February 2012 Morning

Candidate number. Centre number

THIS IS A NEW SPECIFICATION

A Level Chemistry A H432/03 Unified chemistry. Practice paper Set 1 Time allowed: 1 hour 30 minutes

GCSE (9 1) Combined Science (Chemistry) A (Gateway Science) J250/09 Paper 9, C1 C3 and CS7 (PAGs C1 C5)

CHEMISTRY (SALTERS) 2849/01 Chemistry of Materials

A.M. MONDAY, 7 June hours

OXFORD CAMBRIDGE AND RSA EXAMINATIONS GCSE TWENTY FIRST CENTURY SCIENCE A173/02. CHEMISTRY A / FURTHER ADDITIONAL SCIENCE A Module C7 (Higher Tier)

G484. PHYSICS A The Newtonian World ADVANCED GCE. Monday 27 June 2011 Morning. Duration: 1 hour

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

A Level Chemistry B (Salters) H433/02 Scientific literacy in chemistry. Practice paper Set 1 Time allowed: 2 hours 15 minutes

Transcription:

Thursday 19 January 2012 Afternoon AS GE EMISTRY A F322 hains, Energy and Resources *F314440112* andidates answer on the Question Paper. OR supplied materials: Data Sheet for hemistry A (inserted) Other materials required: Scientific calculator Duration: 1 hour 45 minutes * F 3 2 2 * INSTRUTIONS TO ANDIDATES The Insert will be found in the centre of this document. Write your name, centre number and candidate number in the boxes above. Please write clearly and in capital letters. Use black ink. B pencil may be used for graphs and diagrams only. Answer all the questions. Read each question carefully. Make sure you know what you have to do before starting your answer. Write your answer to each question in the space provided. If additional space is required, you should use the lined pages at the end of this booklet. The question number(s) must be clearly shown. Do not write in the bar codes. INFORMATION FOR ANDIDATES The number of marks is given in brackets [ ] at the end of each question or part question. Where you see this icon you will be awarded marks for the quality of written communication in your answer. This means for example you should: ensure that text is legible and that spelling, punctuation and grammar are accurate so that meaning is clear; organise information clearly and coherently, using specialist vocabulary when appropriate. You may use a scientific calculator. A copy of the Data Sheet for hemistry A is provided as an insert with this question paper. You are advised to show all the steps in any calculations. The total number of marks for this paper is 100. This document consists of 24 pages. Any blank pages are indicated. OR 2012 [/500/7834] D (LEO/SW) 40572/6 OR is an exempt harity Turn over

2 Answer all the questions. 1 rude oil is a source of many hydrocarbons. The skeletal formulae of some of these hydrocarbons are shown below. A B D E F G I (a) Explain why compound A is both saturated and a hydrocarbon.... [2] (b) What is the empirical formula for compound A?... [1] (c) Give the letters, A, B,, D, E, F, G, or I, of two hydrocarbons that are structural isomers of each other.... and... [1] OR 2012

3 (d) The petroleum industry processes straight chain alkanes into cyclic hydrocarbons such as A, B and E. (i) Explain why the petroleum industry processes straight chain alkanes into cyclic hydrocarbons.... [1] (ii) ydrocarbon can be processed into the cyclic hydrocarbon B. onstruct an equation for this reaction. [1] (e) Explain why hydrocarbon D has a higher boiling point than hydrocarbon.... [2] (f) ydrocarbons G and are stereoisomers of each other. Explain what is meant by the term stereoisomerism.... [2] (g) onstruct the equation for the complete combustion of hydrocarbon.... [2] OR 2012 Turn over

4 (h) A hydrocarbon molecule, 16 34, is cracked to form an octane molecule and two molecules of but-2-ene. onstruct the equation for this reaction.... [1] (i) ompound I is 3-methylheptane. It does not contain a functional group. I (i) What is meant by the term functional group?... [1] (ii) ompound I reacts with chlorine in the presence of ultraviolet radiation to give several structural isomers of 8 17 l. ow many structural isomers could be formed in this reaction?... [1] (iii) The mechanism of the reaction involves radicals. What is meant by the term radical?... [1] [Total: 16] OR 2012

2 Ethanoic acid, 3 OO, is used to make esters. Some information about two of the processes used to make ethanoic acid is given below. 5 Process 1 This is a one-step process that involves the reaction of methanol with carbon monoxide. 3 O + O 3 OO The conditions used are 180 and 30 atmospheres pressure. A rhodium/iodine catalyst is used. The percentage yield for this process is 99%. Process 2 This involves the oxidation of naphtha, a fraction obtained from crude oil. Liquid naphtha is oxidised using air at a temperature of 180 and 50 atmospheres pressure. No catalyst is needed. A large variety of other products are also formed in this oxidation. (a) Suggest three advantages of making ethanoic acid using Process 1 rather than Process 2.... [3] OR 2012 Turn over

6 (b) The other products formed in Process 2 are carboxylic acids, aldehydes and ketones. A research chemist investigates some of these other products of Process 2. (i) The research chemist isolates product, J. The infrared spectrum of J is shown below. 100 transmittance (%) 50 0 4000 3000 2000 1500 wavenumber / cm 1 1000 500 The chemist also finds that 0.172 g of a pure sample of J contains 2.00 10 3 mol of J. Suggest, with reasons, one possible structure for J. In your answer you should link the evidence with your explanation.... [5] OR 2012

7 (ii) The chemist isolates another product, the carboxylic acid, K. K has the molecular formula 4 8 O 2. Suggest a possible structure and name for K. structure name... [2] (c) Ethanoic acid is used in the manufacture of the ester, propyl ethanoate. Describe how ethanoic acid is converted into propyl ethanoate. Include an equation in your answer.... [4] [Total: 14] OR 2012 Turn over

3 Enthalpy changes can be determined directly or indirectly. (a) A student investigates the reaction between magnesium and dilute hydrochloric acid. 8 Mg(s) + 2l(aq) Mgl 2 (aq) + 2 (g) The student determines the enthalpy change for this reaction. In her experiment, she reacts 0.486 g of magnesium with 50.0 cm 3 of 2.00 mol dm 3 l(aq). The l(aq) is in excess. The temperature of the solution changes from 19.2 to 32.0. (i) alculate the energy released, in kj, during this reaction. The specific heat capacity of the solution = 4.18 J g 1 K 1. The density of the solution is 1.00 g cm 3. energy =...kj [2] (ii) alculate the amount, in moles, of magnesium used by the student. amount =... mol [1] (iii) alculate the enthalpy change of reaction. Give your answer to three significant figures. enthalpy change of reaction =...kj mol 1 [3] OR 2012

9 (b) The student wants to determine the enthalpy change of formation of calcium carbonate, ao 3 (s). a(s) + (s) + 1½O 2 (g) ao 3 (s) (i) What is meant by the term standard enthalpy change of formation? You should state the standard conditions in your answer.... [3] (ii) Using the following data and enthalpy cycle, fill in the boxes on the enthalpy cycle with the correct enthalpy change values calculate the enthalpy change of formation, Δ f, of ao 3 (s). reaction enthalpy change, Δ / kj mol 1 (s) + O 2 (g) O 2 (g) 393 2 (g) + ½O 2 (g) 2 O(l) 285 ao 3 (s) + 2l(aq) al 2 (aq) + 2 O(l) + O 2 (g) 54 a(s) + 2l(aq) al 2 (aq) + 2 (g) 168 a(s) + 2l(aq) + (s) + 1½O 2 (g) f ao 3 (s) + 2l(aq)... al 2 (aq) + 2 (g) + (s) + 1½O 2 (g)...... al 2 (aq) + 2 O(I) + (s) + O 2 (g) al 2 (aq) + 2 O(I) + O 2 (g)... Δ f =... kj mol 1 [3] OR 2012 [Total: 12] Turn over

10 4 ydrogen and chlorine are reacted together to form hydrogen chloride. 2 (g) + l 2 (g) 2l(g) Δ = 184 kj mol 1 (a) alculate the bond enthalpy for the l bond using the information in the table below. bond bond enthalpy / kj mol 1 +436 l l +243 bond enthalpy =... kj mol 1 [2] (b) The reaction is repeated at a higher pressure. Describe and explain what happens to the rate of the reaction between 2 (g) and l 2 (g).... [2] OR 2012

(c) The reaction is repeated again. This time the temperature is decreased. 11 Describe and explain, by drawing appropriately labelled Boltzmann distributions, what happens to the rate of reaction between 2 (g) and l 2 (g).... [5] (d) The mechanism of the reaction between 2 (g) and l 2 (g) involves initiation, propagation and termination. (i) The initiation step is the homolytic fission of the covalent bond in a chlorine molecule. Write an equation to show this homolytic fission.... [1] (ii) omplete the following equations which show the propagation steps. l + 2... +... + l 2... +... [2] (iii) Suggest equations for two termination steps.... [2] [Total: 14] OR 2012 Turn over

5 Sulfuric acid is made from sulfur, oxygen and water in a three-stage process. This can be represented by the following overall equation. 12 2S(s) + 3O 2 (g) + 2 2 O(l) 2 2 SO 4 (l) (a) Explain why the overall process to make sulfuric acid has an atom economy of 100%.... [1] (b) A factory uses 51.4 tonnes of sulfur to manufacture 147 tonnes of 2 SO 4. What is the percentage yield of 2 SO 4? Give your answer to two significant figures. (1 tonne = 1 10 6 g) percentage yield =... % [3] OR 2012

13 (c) One of the reactions involved in making sulfuric acid converts sulfur dioxide, SO 2, into sulfur trioxide, SO 3. 2SO 2 (g) + O 2 (g) 2SO 3 (g) Δ = 197 kj mol 1 This reaction can be carried out at 450 and 3 atmospheres pressure in the presence of a V 2 O 5 catalyst. Under these conditions the position of equilibrium is almost completely on the right-hand side. (i) A research chemist investigates this reaction. e uses a temperature of 450 and 3 atmospheres pressure. The research chemist does not use the catalyst. Predict the changes, if any, on each of the following. position of equilibrium... rate of backward reaction... [2] (ii) The temperature of the reaction mixture is increased to 600. State and explain what will happen to the position of equilibrium.... [1] (iii) The pressure of the reaction mixture is decreased to 2 atmospheres. State and explain what will happen to the position of equilibrium.... [1] OR 2012 Turn over

14 (d) oncentrated 2 SO 4 is used as an acid catalyst in the elimination of water from alcohols. There are several alcohols that are structural isomers with the formula 5 11 O. When these alcohols are heated with 2 SO 4 they form alkenes. 5 11 O 5 10 + 2 O (i) Pentan-1-ol is a structural isomer of 5 11 O that is a primary alcohol. Draw the structure of another structural isomer of 5 11 O that is a primary alcohol. [1] (ii) Pentan-2-ol is a structural isomer of 5 11 O that is a secondary alcohol. Pentan-2-ol is heated with 2 SO 4. Three alkenes are formed, L, M and N. L and M are stereoisomers. N is a structural isomer of the stereoisomers L and M. Draw the structures for alkenes L, M and N. alkene L alkene M alkene N [3] OR 2012

(iii) 15 One structural isomer of 5 11 O is an alcohol that cannot be oxidised by heating with acidified potassium dichromate(vi). Draw the structure of this alcohol. [1] [Total: 13] OR 2012 Turn over

6 Mass spectrometry is used in analysis. 16 (a) ompound O contains carbon, hydrogen and oxygen. The mass spectrum of compound O is shown below. 100 80 60 relative abundance (%) 40 20 0 10 15 20 25 30 m / z 35 40 45 (i) Identify the m/z value that corresponds to the molecular ion.... [1] (ii) Write the formula of the ion that gives rise to the peak at m / z = 31.... [1] (iii) Suggest the molecular formula for O.... [1] OR 2012

17 (b) A scientist analyses a sample of Moon rock. She uses mass spectrometry to find out which metal the sample contains. The mass spectrum of the sample shows m/z peaks as shown in the table. m/z value percentage abundance (%) 63 72.2 65 27.8 Positive ions, X +, of the metal were responsible for the two m/z peaks. Identify the metal X by calculating its relative atomic mass to one decimal place. relative atomic mass of X =... metal X =... [3] [Total: 6] OR 2012 Turn over

18 7 hlorofluorocarbons, Fs, were once used as propellants in aerosols. Fs contribute to ozone depletion in the upper atmosphere. (a) A F has the formula F 2 l 2. State the three-dimensional shape of a F 2 l 2 molecule and the F l bond angle. shape... bond angle... [2] (b) Two reasons that F 2 l 2 was used as an aerosol propellant are that it has low reactivity and will not hydrolyse in water. (i) State one other reason why F 2 l 2 was developed for use as an aerosol.... [1] (ii) Suggest why F 2 l 2 does not hydrolyse in water.... [1] (c) Explain, with the aid of equations, how the presence of Fs in the upper atmosphere leads to ozone depletion.... [3] (d) Why are scientists concerned about ozone depletion?... [1] OR 2012

19 (e) International agreements have reduced the use of Fs. owever the concentration of atmospheric Fs has hardly changed. Suggest two reasons why.... [2] [Total: 10] OR 2012 Turn over

8 yclopentene is a cyclic alkene. 20 (a) The flowchart shows some reactions involving cyclopentene and cyclopentanol. omplete the partial structures in the boxes to show compounds P, Q and R, the main organic products of the reactions. O K 2 r 2 O 7 (aq) / 2 SO 4 (aq) reflux cyclopentanol compound P cyclopentene Br 2 2 with Ni catalyst compound Q compound R [3] (b) What would be the colour change in the reaction between cyclopentene and bromine?... to... [1] OR 2012

21 (c) yclopentene can be polymerised to give poly(cyclopentene). Draw a section of poly(cyclopentene) to show two repeat units. [1] (d) yclopentene reacts with l by electrophilic addition. Use the curly arrow model to complete the mechanism for this reaction. In your answer include any relevant dipoles, the intermediate and the product. 2 2 2 l intermediate product [5] TURN OVER FOR QUESTION 8(e) OR 2012 Turn over

(e) hlorocyclopentane can be hydrolysed by heating with aqueous sodium hydroxide. 22 2 2 2 2 l + NaO 2 2 2 2 O + Nal Use the curly arrow model to complete the mechanism for this hydrolysis reaction. Include in your answer, relevant dipoles, the name of the mechanism and the type of bond fission. In your answer you should use the correct technical terms, spelled correctly. 2 2 2 2 2 2 l 2 2 O +... O products name of mechanism... type of bond fission... [5] [Total: 15] END OF QUESTION PAPER OR 2012

23 ADDITIONAL PAGE If additional space is required, you should use the lined pages below. The question number(s) must be clearly shown. OR 2012

24 ADDITIONAL PAGE opyright Information OR is committed to seeking permission to reproduce all third-party content that it uses in its assessment materials. OR has attempted to identify and contact all copyright holders whose work is used in this paper. To avoid the issue of disclosure of answer-related information to candidates, all copyright acknowledgements are reproduced in the OR opyright Acknowledgements Booklet. This is produced for each series of examinations and is freely available to download from our public website (www.ocr.org.uk) after the live examination series. If OR has unwittingly failed to correctly acknowledge or clear any third-party content in this assessment material, OR will be happy to correct its mistake at the earliest possible opportunity. For queries or further information please contact the opyright Team, First Floor, 9 ills Road, ambridge B2 1GE. OR is part of the ambridge Assessment Group; ambridge Assessment is the brand name of University of ambridge Local Examinations Syndicate (ULES), which is itself a department of the University of ambridge. OR 2012