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

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ADVANED GE HEMISTRY B (SALTERS) hemistry of Materials F334 *E/26423* andidates answer on the question paper. A calculator may be used for this paper. R supplied materials: Data Sheet for hemistry B (Salters) (inserted) ther materials required: Scientific calculator Friday 24 June 2011 Morning Duration: 1 hour 30 minutes * F 3 3 4 * INSTRUTINS T 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. Pencil may be used for graphs and diagrams only. 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. Additional paper may be used if necessary but you must clearly show your candidate number, centre number and question number(s). Answer all the questions. Do not write in the bar codes. INFRMATIN FR 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 B (Salters) 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 90. This document consists of 20 pages. Any blank pages are indicated. [F/500/7968] D (SM/SW) 26423/4 R is an exempt harity Turn over

2 Answer all the questions. 1 Poor processing or storage of wine can lead to the build-up of certain compounds that can spoil the flavour and aroma of the wine. The structures of three such compounds are shown below. H A B (a) (i) Give the systematic name of compound A. (ii) A student wanted to make a sample of compound A from ethanol in the laboratory. Give the reagents that would be mixed with ethanol. State how compound A could be obtained from the reaction mixture.... [3]

(iii) 3 The infrared spectrum of the purified product, shown below, indicates that the student was not successful in converting ethanol to compound A. 100 transmittance (%) 50 0 4000 3000 2000 1500 wavenumber / cm 1 1000 500 Give reasons why the spectrum shows that the product was neither unreacted ethanol nor compound A. Use the spectrum to identify the product. reason product was not ethanol... reason product was not compound A... product is... [3] (iv) Suggest and explain one reason why the student did not obtain compound A.... [2] Turn over

4 H A B (b) (i) Name the functional group in compound. (ii) The reaction that takes place in wine to form compound involves enzymes. Using structural formulae, give the equation for the reaction that takes place in wine in which ethanol forms compound. 2 H 5 H [2] (iii) When the reaction in (ii) is carried out in the laboratory, an additional compound is added to the mixture. Name this compound and suggest one reason why it is used.... [2] (iv) Suggest one advantage of using enzymes over laboratory reagents to prepare organic compounds on an industrial scale.

5 (c) Some people lack an effective enzyme to convert compound A to compound B in the body. This results in more severe hangovers. The enzyme is less effective as a result of damaged DNA. ne way that DNA can be damaged is by an alteration in the sequence of bases. Describe and explain how this damage could result in enzymes becoming less effective for a particular reaction. In your answer you should indicate the importance of the structure of an enzyme to its effectiveness with a particular substrate............................ [6] [Total: 21] Turn over

6 BLANK PAGE PLEASE D NT WRITE N THIS PAGE

7 2 Poly(methyl methacrylate) (PMMA) and poly(methyl acrylate) (PMA) are thermoplastic polymers. Some of their properties and their repeating units are shown in the table below. abbreviation for polymer property of polymer at room temperature T g of polymer / repeating unit of polymer PMA white rubbery H 9 H H 3 H PMMA transparent brittle H H 3 114 H H 3 (a) (i) Explain how the T g data indicate that at room temperature PMA is flexible and PMMA is brittle.... [2] (ii) Suggest a reason why the extra methyl group in PMMA alters the flexibility of the polymer. (iii) Give one way that PMMA could be modified to make it more flexible. Turn over

8 (b) The starting chemical for making the monomer for PMMA is propene. Propene is first converted into propanone which is then converted into compound D. H H 3 H H 2 H 3 H 3 H 3 H 3 N propene propanone compound D (i) At room temperature propene is a gas but propanone is a liquid. Explain, in terms of intermolecular bonds, the difference in the boiling points of propene and propanone.... [4] (ii) Give the reagent used in the laboratory to convert propanone into compound D. (iii) Draw the two step mechanism for the formation of compound D from propanone, using curly arrows and bond polarities where appropriate. [4]

9 (iv) Explain why the N group in compound D is attached to the carbon chain by a bond rather than by a N bond. (v) The industrial conversion of propanone to compound D is an addition reaction. In what respect are addition reactions environmentally friendly? (c) Another useful polymer similar to PMMA is PMMAA. Its monomer can be made by the reactions shown below. H 3 H 3 H 3 reaction 1 H NH 2 H 2 H 3 H 2 H 2 MMA (monomer of PMMA) MMAA (monomer of PMMAA) (i) Give the reagent and conditions for reaction 1. reagent... conditions... [2] (ii) Name the functional group present in MMAA other than the = bond. Turn over

(iii) 10 ompound F is a structural isomer of MMAA. H 3 H 2 NH 2 MMAA H 3 H NH 2 H compound F Will either compound F or MMAA or both show E/Z isomerism? Explain your answer.... [2] [Total: 20]

11 3 Tyrosine and threonine are two amino acids used in the construction of proteins. Their R groups both contain hydroxyl groups. Their structures are shown below. H H 2 NH 2 NH 2 H H 3 H H H H H tyrosine threonine (a) State how the hydroxyl groups are different in tyrosine and threonine and give a chemical test to distinguish between them. Describe what you would see in each case................ [4] (b) Tyrosine and threonine are chiral molecules. n the diagrams above circle all of the chiral carbon atoms in each structure. [2] (c) Threonine can form a condensation polymer containing amine side chains. Draw the repeating unit for this polymer and give the name of the link joining the monomer units together. name of link... [2] Turn over

12 (d) In foodstuffs such as cheese, tyrosine decays into tyramine. Tyramine is possibly responsible for migraine-type headaches. H tyramine NH 2 (i) omplete the table below to show the structures of the products formed when tyramine reacts with the named reagents. reagent product(s) formed hydrochloric acid ethanoyl chloride [5] (ii) Although tyramine is not very soluble in water it will dissolve if a little aqueous alkali is added to a mixture of tyramine and water. Explain why tyramine is able to do this.... [2] [Total: 15]

13 4 Potassium manganate(vii) can be used as a disinfectant. ver time, the concentration of potassium manganate(vii) in dilute aqueous solution decreases due to a redox reaction taking place in the sealed bottles. xygen is also formed in this reaction. (a) Suggest the reducing agent responsible for the decrease in concentration of potassium manganate(vii) solutions on storage in sealed bottles.... [1] (b) Solutions of potassium manganate(vii) can be standardised against a measured volume of a standard solution of sodium ethanedioate, Na 2 2 4, under acid conditions. The contents of the titration flask have to be warmed to 60 before commencing the titration, otherwise the reaction would be too slow. (i) Describe how you would carry out this titration to get one result. In your answer you should use appropriate technical terms spelled correctly.... [5] Turn over

(ii) 14 In a titration, a student used a sodium ethanedioate solution with a concentration of 0.0500 mol dm 3. alculate the mass of sodium ethanedioate (Na 2 2 4 ) needed to make 250 cm 3 of a 0.0500 mol dm 3 solution. mass of sodium ethanedioate =... g [2] (iii) The student found that 10.0 cm 3 of the 0.0500 mol dm 3 sodium ethanedioate solution reacted exactly with 26.0 cm 3 of a potassium manganate(vii) solution. The equation for the reaction is given below. 2Mn 4 (aq) + 5 2 2 4 (aq) + 16H + (aq) 2Mn 2+ (aq) + 10 2 (g) + 8H 2 (l) alculate the concentration of the potassium manganate(vii) solution. Give your answer to an appropriate number of significant figures. concentration of potassium manganate(vii) solution =... mol dm 3 [4]

15 (c) The student found that the rate of reaction between Mn 4 and 2 4 2 ions could be increased at room temperature sufficiently to carry out an accurate titration without warming the solution. The student did this by adding a few drops of an aqueous solution containing u 2+ ions to the titration flask. (i) Explain how transition metal ions such as u 2+ are able to increase the rate of a redox reaction.... [4] (ii) What name is given to this type of catalysis by aqueous transition metal ions? Turn over

16 (d) The student investigated the rate of reaction between Mn 4 and 2 4 2 ions in aqueous acid, in the presence of a small concentration of u 2+. In order to investigate the order of reaction with respect to Mn 4, the initial concentrations of 2 4 2 and H + were made much larger than the Mn 4 concentration. The results are shown in the graph below. 1.2 1.1 1 0.9 [Mn 4 ] / 10 3 mol dm 3 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 0 10 20 30 40 50 time / s 60 70 80 90 100 (i) Why did the student use initial concentrations of 2 4 2 and H + that were much larger than the Mn 4 concentration?

17 (ii) Use the graph to show that the reaction is first-order with respect to Mn 4. You should draw any appropriate construction lines on the graph.... [3] (iii) Under the conditions of the reaction, the rate equation can be represented as shown below. rate = k [Mn 4 ] With a concentration of Mn 4 of 1.20 10 3 mol dm 3, the student found that the rate of reaction was 6.7 10 4 mol dm 3 s 1. alculate the value of k for this reaction and give its units. k =... units =...[3] [Total: 24] Turn over

18 5 Early 19th century chemists attempted to protect copper structures from corrosion by strapping blocks of iron to them. This method was especially effective for structures immersed in seawater. The iron would turn into a red brown solid. (a) (i) By drawing arrows in the appropriate boxes, complete the outer electron structures for u and u 2+. 3d 4s u u 2+ [2] (ii) Use your answer to (i) to explain why copper is a transition metal. (b) Some standard electrode potential data are given below. half-reaction E o /V Fe 2+ (aq) + 2e Fe(s) u 2+ (aq) + 2e u(s) 2 (g) + 2H 2 (l) + 4e 4H (aq) Fe 3+ (aq) + e Fe 2+ (aq) 0.44 +0.34 +0.40 +0.77 (i) Use data from the table to explain why copper corrodes in water containing dissolved oxygen.... [2] (ii) Use data from the table to explain how the iron prevents the copper from corroding.

19 (c) The reaction of Fe 3+ ions in solution with excess hydroxide ions produces another red brown solid. Give the ionic equation for the formation of this red brown solid. Include state symbols. [2] (d) Describe and explain one other method for protecting copper from corrosion.......... [2] [Total: 10] END F QUESTIN PAPER

20 PLEASE D NT WRITE N THIS PAGE opyright Information R is committed to seeking permission to reproduce all third-party content that it uses in its assessment materials. R 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 R 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 R has unwittingly failed to correctly acknowledge or clear any third-party content in this assessment material, R 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 Hills Road, ambridge B2 1GE. R 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.