Monday 14 January 2013 Afternoon

Similar documents
Wednesday 19 June 2013 Morning

Tuesday 14 June 2016 Afternoon

Tuesday 19 June 2012 Afternoon

Tuesday 13 June 2017 Afternoon

Tuesday 2 June 2015 Afternoon

CHEMISTRY (SALTERS) 2849/01 Chemistry of Materials

Friday 26 May 2017 Morning

Thursday 10 January 2013 Morning

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

THIS IS A NEW SPECIFICATION

Wednesday 16 January 2013 Morning

Friday 27 May 2016 Morning

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

CHEMISTRY 2815/01 Trends and Patterns

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

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

Tuesday 22 January 2013 Afternoon

Thursday 26 January 2012 Afternoon

2 Answer all the questions. 1 PLA is a biodegradable polymer made from corn starch. The structure of part of a PLA chain is shown below.

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

CHEMISTRY 2816/01 Unifying Concepts in Chemistry

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 F321 CHEMISTRY A. Atoms, Bonds and Groups

THIS IS A NEW SPECIFICATION

Monday 19 June 2017 Morning

Thursday 10 January 2013 Morning

Thursday 23 May 2013 Morning

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

Monday 19 June 2017 Morning

* * MATHEMATICS 4721 Core Mathematics 1 ADVANCED SUBSIDIARY GCE. Monday 11 January 2010 Morning QUESTION PAPER. Duration: 1 hour 30 minutes.

Tuesday 14 June 2016 Afternoon

Wednesday 21 May 2014 Afternoon

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

Thursday 19 January 2012 Afternoon

Tuesday 4 June 2013 Afternoon

Wednesday 23 May 2012 Afternoon

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

Candidate number. Centre number

Friday 10 June 2016 Afternoon

THIS IS A NEW SPECIFICATION

THIS IS A NEW SPECIFICATION

CHEMISTRY (SALTERS) 2849/01 Chemistry of Materials

Tuesday 10 June 2014 Morning

Wednesday 10 June 2015 Afternoon

Wednesday 13 June 2012 Morning

THIS IS A NEW SPECIFICATION

Thursday 19 January 2012 Afternoon

Wednesday 16 January 2013 Morning

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

Monday 18 June 2012 Morning

THIS IS A NEW SPECIFICATION

CHEMISTRY 2812/01 Chains and Rings

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

CHEMISTRY 2814/01 Chains, Rings and Spectroscopy

Wednesday 16 January 2013 Morning

Tuesday 2 June 2015 Afternoon

Tuesday 4 June 2013 Afternoon

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

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

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

Friday 23 June 2017 Morning

CHEMISTRY 2814/01 Chains, Rings and Spectroscopy

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

Candidate number. Centre number

THIS IS A NEW SPECIFICATION

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

THIS IS A NEW SPECIFICATION

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

THIS IS A NEW SPECIFICATION MODIFIED LANGUAGE

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

GCSE (9 1) Combined Science A (Gateway Science)

Wednesday 8 June 2016 Afternoon

Tuesday 24 May 2016 Morning

MATHEMATICS 4725 Further Pure Mathematics 1

Monday 23 May 2016 Morning

Wednesday 1 February 2012 Morning

Monday 20 June 2016 Morning

G491. PHYSICS B (ADVANCING PHYSICS) Physics in Action ADVANCED SUBSIDIARY GCE. Wednesday 12 January 2011 Morning. Duration: 1 hour

THIS IS A NEW SPECIFICATION MODIFIED LANGUAGE

Thursday 17 May 2012 Morning

CHEMISTRY (SALTERS) Chemistry of Materials. OXFORD CAMBRIDGE AND RSA EXAMINATIONS Advanced GCE

CHEMISTRY (SALTERS) 2854/01 Chemistry by Design

Afternoon. Data Sheet for Chemistry (Salters) (Inserted)

THIS IS A NEW SPECIFICATION MODIFIED LANGUAGE

Tuesday 23 May 2017 Morning

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 F332/TEST CHEMISTRY B (SALTERS) Chemistry of Natural Resources

Monday 20 June 2016 Morning

CHEMISTRY 2815/01 Trends and Patterns

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

Thursday 9 June 2016 Afternoon

Thursday 16 June 2016 Morning

CHEMISTRY (SALTERS) 2849

Thursday 11 June 2015 Morning

G494. PHYSICS B (ADVANCING PHYSICS) Rise and Fall of the Clockwork Universe ADVANCED GCE. Monday 27 June 2011 Morning. Duration: 1 hour 15 minutes

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

Tuesday 27 June 2017 Morning Time allowed: 1 hour 30 minutes

* * MATHEMATICS (MEI) 4757 Further Applications of Advanced Mathematics (FP3) ADVANCED GCE. Wednesday 9 June 2010 Afternoon PMT

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

Thursday 12 June 2014 Afternoon

Transcription:

Monday 14 January 2013 Afternoon A2 GCE CHEMISTRY B (SALTERS) F334/01 Chemistry of Materials *F314560113* Candidates answer on the Question Paper. CR supplied materials: Data Sheet for Chemistry B (Salters) (inserted) ther materials required: Scientific calculator Duration: 1 hour 30 minutes * F 3 3 4 0 1 * INSTRUCTINS T CANDIDATES 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. HB 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. INFRMATIN FR CANDIDATES 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 Chemistry 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] DC (AC/CGW) 58070/4 CR is an exempt Charity Turn over

2 Answer all the questions. 1 To combat the security problems of metal cutlery on aircraft, chemists have developed a polymer known as PPA. This polymer, a polyamide, is strong enough to replace stainless steel cutlery for in-flight use. The following monomers, A and B, can be reacted to make PPA polymer. CH H 2 N NH 2 A CH B (a) Use the formulae above to draw the structural formula of the repeating unit for PPA. [2] (ii) n your diagram circle a secondary amide group. [1] (iii) Name monomer B.... [2]

(b) Nylon-6 is also a polyamide. 3 Nylon-6 has six carbon atoms in its repeating unit and can be made from a single monomer having a straight carbon chain. Suggest a structural formula for this single monomer of nylon-6. [1] (ii) Name and explain the type of polymerisation reaction this monomer undergoes to form nylon-6.... [1] (c) Polyamides have a high proportion of crystalline areas. Explain what is meant by crystalline.... [1] (ii) PPA has more crystalline areas than nylon-6. This gives PPA a greater T m than nylon-6. Explain this greater T m in terms of the intermolecular bonding involved.... [3] (iii) Name a process by which a nylon-6 fibre could be made more crystalline.... [1] Turn over

4 (d) In the manufacture of PPA, monomer B can be made from butane by the following 3-step process. catalyst + 2H 2 step 1 compound C 2HCN step 2 H 2 N monomer B NH 2 4H 2 step 3 NC CN For each step, name the type of reaction taking place by selecting a suitable word from the list below. addition condensation elimination rearrangement substitution step 1... step 2... step 3... [3] (ii) How does the hydrogen produced by step 1 help to reduce the cost of the overall process?... [1] (e) In some countries, compound C is synthesised by first converting ethanol into CH 3 CH. Give the reagents used in a laboratory to convert ethanol into CH 3 CH.... [1] [Total: 17]

5 BLANK PAGE Question 2 begins on page 6 D NT WRITE N THIS PAGE Turn over

6 2 Glycolic acid is widely used in cosmetic skin-care products. It is an odourless and crystalline solid that is very soluble in water. H H glycolic acid (a) Describe and explain how part of the glycolic acid structure acts as an acid.......... [2] (b) The concentration of glycolic acid in a skin-care product is important. Any product containing over 10.0 g of glycolic acid in 100 cm 3 solution is classed as a hazardous material. Acnegone is a solution of glycolic acid. A student carries out an acid base titration using a standard solution of NaH to find out how much glycolic acid is in the Acnegone solution. The student dilutes 14.0 cm 3 of Acnegone with water to form 250 cm 3 of solution. 25.0 cm 3 of this solution reacts exactly with 16.0 cm 3 of 0.250 mol dm 3 aqueous NaH. Complete the equation for the reaction of glycolic acid with sodium hydroxide. CH 2 HCH + [1]

(ii) 7 Calculate the mass of glycolic acid in 100 cm 3 of Acnegone and state whether Acnegone should be classed as a hazardous product. Give your answer to an appropriate number of significant figures. mass of glycolic acid =... g in 100 cm 3 is it classed as hazardous?... [6] (c) Carboxylic acids can be converted to esters. Esters, such as compound D, are often used in varnishes. H 3 C C CH 2 CH 2 CH 2 CH 3 compound D Name compound D and circle the ester group.... [2] (ii) Name the compounds you would heat under reflux with ethanoic acid to form compound D.... [2] (iii) Name the types of intermolecular bonds present in ethanoic acid and compound D. ethanoic acid... compound D... [3] Turn over

8 H 3 C C CH 2 CH 2 CH 2 CH 3 compound D (d) A student attempts to synthesise compound D from ethanoic acid. The student distils off the product and runs an infrared spectrum and a mass spectrum on it. 100 The infrared spectrum is shown below. transmittance (%) 50 2880 2940 1743 1244 0 4000 3000 2000 1500 1000 500 wavenumber / cm 1 Use the IR spectrum and your Data sheet to give two pieces of evidence to show that the product does not contain any starting materials.... [2]

The mass spectrum of the ester is shown below. 9 100 80 relative intensity (%) 60 40 20 0 10 20 30 40 50 60 70 80 90 100 110 120 m /z (ii) Suggest formulae for the following: the chemical species responsible for the peak at m /z 73, the species lost from the molecular ion to form this chemical species. Write your answers in the table below the working space. Formula Species which gives the peak at m /z 73 Species lost from the molecular ion [3] Turn over

10 (e) Glycolic acid can be made from methanal. Methanal is first reacted with cyanide ions in aqueous solution to form a cyanohydrin. H H C H C H H CN Underline two of the following words which describe the mechanism of the reaction described above. addition condensation electrophilic elimination nucleophilic radical substitution [2] (ii) Describe the mechanism of the reaction using curly arrows, bond polarities and relevant lone pairs of electrons. [5] [Total: 28]

11 3 DNA and proteins are polymers made up of long chains of monomer units. At one time proteins were considered more likely than DNA to transmit genetic data. (a) Name the monomer units in DNA and the components of which they are made.... [2] (ii) Name the monomer units in proteins.... [1] (iii) Suggest why scientists once thought that proteins were more likely to transmit genetic data.... [2] (b) Hydrogen bonding is important in base pairing in DNA. Complete the structure of adenine in the diagram below using your Data Sheet. Show how adenine hydrogen bonds with thymine. Show any relevant lone pairs of electrons and partial charges. CH 3 DNA chain N N H thymine N N N adenine N DNA chain [3] Turn over

(c) The diagram below shows part of the primary structure of an enzyme. 12 H H N H 2 C C H N CH C H N C C CH 2 H 3 C CH H H n the diagram circle two chiral carbon atoms. [1] (ii) Proteins are hydrolysed by refluxing with aqueous NaH. n the diagram above draw arrows pointing to the bonds that will break in the two full peptide links in the structure. [1] (iii) Draw the structural formula of the complete ion formed by breaking these peptide links in alkaline solution. [2] (iv) As well as having a primary structure, enzymes also have secondary and tertiary structures. What is meant by the secondary structure and the tertiary structure of an enzyme? secondary... tertiary...... [2] [Total: 14]

13 4 A common way of cleaning laboratory glassware is by dipping it in a bath containing acidified potassium dichromate(vi), often called chromic acid, which is a powerful oxidising agent. However, such use of compounds containing heavy metal ions is considered hazardous. Nochromix is a metal-free alternative to chromic acid. It consists of ammonium peroxodisulfate crystals. These are white crystals that are very soluble in water, forming a solution which can also act as a strong oxidising agent. (a) The diagram shows the arrangement of atoms in a peroxodisulfate ion, S 2 8 2. Complete the diagram to show a dot-and-cross representation of the peroxodisulfate ion. XX X X X X 2 S X XX X X S XX XX X X X X X XX (ii) represents the extra electrons required to form the ion Give the formula of ammonium peroxodisulfate. [2]... [1] (b) Use the data in the table below to decide which of the two oxidising agents, Cr 2 7 2 /H + and S 2 8 2, is the stronger under standard conditions. Give your reasoning. Half-reaction E o /V Cr 2 7 2 + 14H + + 6e 2Cr 3+ + 7H 2 +1.33 S 2 8 2 + 2e 2S 4 2 +2.01......... [2] Turn over

14 (c) Peroxodisulfate ions will oxidise iodide ions to iodine in an aqueous solution. The halfequations are shown below. S 2 8 2 + 2e 2S 4 2 2I I 2 + 2e Write an ionic equation for the reaction between peroxodisulfate and iodide ions. State symbols are not required. [1] (ii) A student investigates the rate of this reaction at room temperature by using a colorimeter. The student performs one experiment only in which a large excess of peroxodisulfate ions to iodide ions is used. The student has a flask in which the reagents are mixed. Describe how the student could use a colorimeter to measure the concentrations of iodine in the flask as the reaction proceeds. In your answer: Describe the procedures the student would carry out. Assume that samples of required solutions are available. State the measurements that would be recorded and indicate how these can be converted into concentrations of iodine. In your answer you should use technical terms spelled correctly.... [6]

(iii) 15 The student converts the concentrations of iodine into concentrations of iodide remaining. The student then uses a time concentration graph to show that the reaction is first-order with respect to iodide ions. Sketch a curve and indicate on the graph how the reaction can be shown to be first-order. [iodide ions] time [3] Question 4 continues on page 16 Turn over

16 (d) The student investigates whether transition metal ions would catalyse the reaction between S 2 8 2 and I ions. The student uses the data in the table below to decide if the use of Fe 3+ ions might speed the reaction up. Half-reaction E o /V I 2 + 2e 2I Fe 3+ + e Fe 2+ S 2 2 8 + 2e 2S 2 4 +0.54 +0.77 +2.01 Name the type of catalysis the student is investigating. Give a reason for your answer.... [1] (ii) Complete the electron structures for Fe 2+ and Fe 3+. Fe 2+ 1s 2 2s 2 2p 6... Fe 3+ 1s 2 2s 2 2p 6... [2] (iii) Use the table of data to explain why adding Fe 3+ ions to the mixture of I and S 2 8 2 ions provides an alternative route for this reaction. Include ionic equations for any reactions you describe. In your answer you should explain how the data from the table are linked to the reactions you describe.... [6]

(e) The student s results for the uncatalysed reaction are given below. 17 [I ] Rate of formation Experiment [S 2 2 8 ] / mol dm 3 / mol dm 3 of iodine, I 2 / mol dm 3 s 1 1 0.075 0.040 2.0 10 5 2 0.150 0.040 4.0 10 5 3 0.075 0.020 1.0 10 5 Complete the rate equation for the reaction. Rate = k [2] (ii) Calculate the rate constant, k, for the reaction and give its units. k =... units... [3] (iii) What would be the rate of disappearance of I in experiment 3?... [2] [Total: 31] END F QUESTIN PAPER

18 ADDITINAL ANSWER SPACE If additional answer space is required, you should use the following lined page(s). The question number(s) must be clearly shown in the margins.

19

20 Copyright Information CR is committed to seeking permission to reproduce all third-party content that it uses in its assessment materials. CR 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 CR Copyright 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 CR has unwittingly failed to correctly acknowledge or clear any third-party content in this assessment material, CR will be happy to correct its mistake at the earliest possible opportunity. For queries or further information please contact the Copyright Team, First Floor, 9 Hills Road, Cambridge CB2 1GE. CR is part of the Cambridge Assessment Group; Cambridge Assessment is the brand name of University of Cambridge Local Examinations Syndicate (UCLES), which is itself a department of the University of Cambridge.