ReviewQuestions-G12-Edexcel-Unit-5

Similar documents
(a) (i) Explain what is meant by the terms transition element, complex ion and ligand,

Write an overall equation for the first stage in the rusting of iron.

Hydrated nickel(ii) salts are green in colour. Give the electron configuration of a nickel(ii) ion and hence state why the ion is coloured.

For the element X in the ionic compound MX, explain the meaning of the term oxidation state.

Paper Reference. (including synoptic assessment) Thursday 11 June 2009 Afternoon Time: 1 hour 30 minutes

CHEMISTRY HIGHER LEVEL

CHEMISTRY HIGHER LEVEL

1. This question is about Group 7 of the Periodic Table - the halogens. The standard electrode potentials for these elements are given below.

AQA A2 CHEMISTRY TOPIC 5.4 TRANSITION METALS PART 2 REDOX REACTIONS AND CATALYSIS BOOKLET OF PAST EXAMINATION QUESTIONS

Show by calculation that the starting concentration of the manganate(vii) ions was mol dm 3.

EXPERIMENTS. Testing products of combustion: Reducing Copper(III) Oxide to Copper. Page 4

Topic 5 Transition Elements Revision Notes

Identification of ions and gases

Paper Reference. Advanced Unit Test 6B (Synoptic) Monday 25 June 2007 Morning Time: 1 hour 30 minutes

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certificate of Education Advanced Subsidiary Level and Advanced Level CHEMISTRY 9701/03

London Examinations GCE

Chem!stry. Assignment on Redox

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

1 Three redox systems, C, D and E are shown in Table 6.1. C Ag(NH 3. ) 2 + (aq) + e Ag(s) + 2NH 3. (aq) D Ag + (aq) + e Ag(s)

*AC222* Chemistry Assessment Unit A2 2. Analytical, Transition Metals, Electrochemistry and Further Organic Chemistry. New Specification.

The presence of these ions can be confirmed by reacting separate samples of solution X with aqueous ammonia and with aqueous sodium carbonate. ...

(08) WMP/Jun10/CHEM5

Identification of Ions and Gases

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

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

flame test acidified silver nitrate solution added

# Ans Workings / Remarks

Chemistry 2.5 AS WORKBOOK. Working to Excellence Working to Excellence

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

AL CHEMISTRY d-block ELEMENTS Exercises from Past Exam Questions

QUESTIONSHEETS INORGANIC CHEMISTRY REACTIONS OF PERIOD 3 ELEMENTS WITH WATER REACTIONS OF PERIOD 3 ELEMENTS WITH OXYGEN

The table shows the results of some tests carried out on three solutions, A, B and C. Hydrochloric acid is added. Solution

AQA A2 CHEMISTRY TOPIC 4.10 ORGANIC SYNTHESIS AND ANALYSIS TOPIC 4.11 STRUCTURE DETERMINATION BOOKLET OF PAST EXAMINATION QUESTIONS

Name: Class: Redox revision questions. 50 minutes. Time: Marks: 50. Comments: Page 1 of 17

Suggested answers to in-text activities and unit-end exercises. Topic 16 Unit 55

Describe the structure and bonding in a metallic element. You should include a labelled diagram in your answer. ... [3] ...

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

CHEMISTRY HIGHER LEVEL

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

UNIT 2 REVISION CHECKLIST. a) understand that reactions are either exothermic or endothermic and apply the sign convention

2 Answer all the questions. CO, in the presence of aqueous hydrochloric acid, HCl(aq).

A-level CHEMISTRY (7405/1)

Paper Reference. Paper Reference(s) 6246/02 Edexcel GCE Chemistry Advanced Unit Test 6B (Synoptic)

MC 17 C - 6 SECTION - I

5.3.1 Transition Elements

Paper Reference. (including synoptic assessment) Monday 23 January 2006 Morning Time: 1 hour 30 minutes

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

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

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

MARAKWET WEST DISTRICT 233/1 CHEMISTRY PAPER 1 JULY/AUGUST 2015 TIME: 2 HOURS


Chemistry Assessment Unit A2 2

AS Paper 1 Group VII: The Halogens

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

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

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

Experiment [RCH 2 Cl] [OH ] Initial rate/mol dm 3 s

(a) A student carries out an investigation based on the redox systems shown in Table 5.1 below. redox system E o / V 1 Ni 2+ (aq) + 2e Ni(s) 0.

Redox. Question Paper. Cambridge International Examinations Chemical Reactions. Score: /43. Percentage: /100

Chemistry Assessment Unit A2 1

PRACTICAL QUESTIONS TEST TUBE REACTIONS 4&11 Questions. Dr Chris Clay

REACTION RATES AND REVERSIBLE REACTIONS

Module 4: Further Organic, Physical and Inorganic Chemistry

least reactive magnesium

Chem!stry. Mole Calculations Assignment Twelve

IGCSE TEST_ (Ch. 2,3,4,5,6) Name... Date...


Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

Secondary School Mathematics & Science Competition Chemistry. Time allowed : 11:45 am - 1:00 pm (1hour 15 minutes) Total marks : 75

Titration curves, labelled E, F, G and H, for combinations of different aqueous solutions of acids and bases are shown below.

CHEMISTRY HIGHER LEVEL

3.2.8 Haloalkanes. Nucleophilic Substitution. 267 minutes. 264 marks. Page 1 of 36

2 Answer all the questions. 1 This question refers to chemistry of d-block elements in Period 4 (Sc Zn).

CHERRY HILL TUITION AQA CHEMISTRY A2 PAPER Section A (2 marks) (1 mark) (Extra space) Property

Unit 5: General Principles of Chemistry II Transition Metals and Organic Nitrogen Chemistry (including synoptic assessment)

for free revision past papers visit:

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

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

CHEMISTRY 2815/01. Trends and Patterns. OXFORD CAMBRIDGE AND RSA EXAMINATIONS Advanced GCE

ICSE Board Class X Chemistry Board Paper Time: 1½ hrs Total Marks: 80

ST EDWARD S OXFORD. Lower Sixth Entrance Assessment. November Chemistry. 1 Hour. Candidates name:... St Edward's School 1

PMT. This question is about the reaction sequence shown below

London Examinations IGCSE

YEAR 10- Chemistry Term 1 plan

A level Chemistry Preparation Work

Advanced Subsidiary Paper 2: Core Organic and Physical Chemistry

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certificate of Education Advanced Subsidiary Level and Advanced Level CHEMISTRY 9701/03

CAMBRIDGE INTERNATIONAL EXAMINATIONS International General Certificate of Secondary Education

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

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

MV18. Chemistry. Centre Number. Candidate Number. Time 2 hours, plus your additional time allowance.

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certificate of Education Ordinary Level

4. a) Complete the nuclear equation below. (1mk) b) 37 37

3.2.5 Group VII. Trends in reducing abilities. 222 minutes. 218 marks. Page 1 of 21

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

Q1. Ammonia is used in the production of fertilisers. The flow diagram shows the main stages in the manufacture of ammonia.

Assessment Unit A2 2 assessing Analytical, Transition Metals, Electrochemistry and Further Organic Chemistry

GCE O' LEVEL PURE CHEMISTRY (5073/02) Suggested Answers for 2016 O Level Pure Chemistry Paper 2

Transcription:

Unit 5 Questions Question 1:Give the electronic configuration of a titanium atom and a Ti3+ ion. Titanium is a transition metal, state what is meant by this on the basis of electronic configuration you gave above. Transition metal elements characteristically have several oxidation states; iron commonly has oxidation state of +2 and +3. but these are not the only ones. Explain why under normal conditions, iron(iii) is more stable than iron(ii). Oxidation of iron with potassium nitrate in alkaline solution gives a red compound, R, which contains potassium, iron and oxygen only. R is a powerful oxidizing agent and will oxidize iron(ii) to iron(iii). 25.0g of a 0.100mol dm -3 solution of R oxidized 37.5cm 3 of a solution of iron(ii) containing 55.6g dm -3 of FeSO 4.7H 2 O. Calculate the oxidation state of the iron in R. suggest a formula for R [answer hint: K 2 FeO 4 is R] Question 2:A student determined the percentage of iron in an iron(ii) salt X, as follows: 1.20g of the salt was placed in a beaker and 50 cm 3 of water was added to dissolved the salt. The solution was heated to boiling point with a small quantity of concentrated nitric acid and eventually it became a yellow colour. One drop of this yellow solution was then extracted and tested by adding one drop of a freshly prepared dilute solution of potassium hexacyanoferrate (III). Potassium hexacyanoferrate (III) solution will react with iron (II) to produce a blue coloration. No such coloration was obtained. Further treatment of the solution included the addition of ammonia solution, a little at a time, with constant stirring, until a slight smell of ammonia persisted. The brown precipitate was separated, washed and then heated strongly to give iron (III) oxide. A further 1.20g sample of X was treated in the same way and in both experiments the mass of iron (III) oxide obtained was 0.245g. Suggest a colour for the iron (II) salt solution. Why was the concentrated nitric acid added? What ion gave rise to the yellow colour in the solution after boiling with concentrated nitric acid? The formula of potassium hexacyanoferrate (III) is K 3 Fe (CN) 6. Write the formula of the complex anion in this compound. Draw a diagram showing the shape of the anion described above and also describe the shape. Why was the hexacyanoferrate (III) test carried out? If a blue colouration had appeared in the test what would the student then have to do? Explain why ammonia solution was added until a slight smell of ammonia persisted. Name the brown precipitate formed on addition of the ammonia solution. Write an ionic equation showing the formation of precipitate. Write the equation for the action of heat on the precipitate. Calculate the mass of iron present in 0.245g of the iron (III) oxide. Calculate the percentage of iron present in X. Question 3:Give the electronic configuration of chromium atom, Cr, Cr 2+ and Cr 3+ ions. How is the electron structure of Cr unusual and why? Calculate the oxidation number of Mn in MnO 2-4. Why does Sc form only Sc 3+ ions? Why are transition metals able to show a variety of oxidation states? Fe 2+ ions will catalyse the reaction between peroxodisulphate ions, and iodide ions which is otherwise slow; the uncatalysed, exothermic reaction is: [S 2 O 2-8 + 2I - 2-2SO 4 + I 2 ] and the catalysed steps are [2Fe 2+ 2- + S 2 O 8 2 SO 2-4 + 2 Fe 3+ ] [2Fe 3+ + 2I - 2Fe 2+ + I 2 ]. Sketch a reaction profiles (enthalpy level diagrams) for both the uncatalysed and the catalysed reactions. Label each profile. Examine the equations for the catalysed steps of the reaction. Suggest why this process is more energetically favourable. On what property of transition metal does the catalyst depend? Question 4:Give the electronic configuration of vanadium and the vanadium ion, V 2+. Suggest why the hydrated ion [V(H 2 O) 6 ] 2+ is coloured? Name the type of bonding within ions of this type. Ammonium vanadate, NH 4 VO 3, dissolves in aqueous sodium hydroxide with the evolution of a colourless gas. The solution becomes yellow after acidification. The gas has a pungent odour and produces a pale blue precipitate with copper (II) sulphate solution. The precipitate dissolves, as more gas is passed in, to give a deep blue solution. Write an ionic equation for the reaction of the cation of NH 4 VO 3 with alkali. Name the pale blue precipitate. Give the formula of the ion responsible for the colour of the deep blue solution. Ammonium vanadate, on treatment with sulphuric acid, gives a yellow colour due to the [VO 2 ] + ion. Addition of zinc to the solution causes the solution colour to ReviewQuestions-G12-Edexcel-Unit-5 Jaydip.Chaudhuri 1

change to blue, then green, then violet. Give the oxidation number of vanadium in the vanadium containing ions in each coloured solution (a) blue solution (b) green solution (c) violet solution. The industrial production of sulphur trioxide from sulphur dioxide and oxygen is catalyzed by vanadium (V) oxide, it has been proposed that the first stage of the reaction is [SO 2 + V 2 O 5 SO 3 + 2VO 2 ]. Write an equation for the second stage, thus showing vanadium (V) oxide as a catalyst. Give the systematic name for each of the ions (a) [VO 2 ] + (b) [Cr(NH 3 ) 4 Cl 2 ] +. Draw and describe the shape of the ions above. Question 5:Define oxidation in terms of the electron transfer. State three properties which distinguish transition metals from main group metals. Give the electronic configurations for Fe and Fe 3+. name the type of reaction involved in the following changes. [Cu(H 2 O) 6 ] 2+ : A (+ NH 3 (aq) ) blue precipitate: B (+excess NH 3 ) deep blue solution :C. give the formula of the compound B. draw the structure of the ion responsible for the colour in solution C and show its shape. Addition of aqueous copper(ii) ions to aqueous iodide ions gives a precipitate of copper(i) iodide and liberates iodine. The iodine can be titrated with aqueous sodium thiosulphate. These reactions from the basis for a volumetric analysis of copper, for example in metal alloys. Write an ionic equation for the reaction of copper(ii) ions with iodide ions. Given that the reaction of iodine with sodium thiosulphate is [I 2 + S 2 O 2-3 I - + S 4 O 2-6 ] find the volume of sodium thiosulphate solution of concentration 1.00 mol dm -3 needed to react with iodine liberated by copper ions from a brass screw of mass 2.00g, containing 60% of copper by mass Question 6:When acidified solution of potassium dichromate(vi), Cr 2 O 2-7 is added to a solution of an iron(ii) compound, the dichromate (VI) ion, Cr 2 O 2-7 are reduced to chromium(iii) ions and iron(ii) are oxidized to iron(iii). Write an ionic half equation for the reduction of dichromate ions in the acidic solution. Write an equation for the reaction between dichromate(vi) and iron(ii) ions. A 0.204g sample of steel reacted with dilute sulphuric acid. The resulting solution required 27.4cm 3 of 0.0220 mol dm -3 potassium dichromate(vi) solution for complete reaction. Calculate the percentage of iron in the sample of steel. Question 7:This equation concerns the compound Q pent-3-en-2-ol, CH 3 CH(OH)CH= CHCH 3, give the structural formula of a compound isomeric with Q which does not contain a carbon-carbon double bond. Q shows two types of stereoisomerism. Draw the geometric isomers of Q and state why Q show this types of isomerism. Draw the optical isomers of Q and state what effect such isomers have on the plane of plane polarized monochromatic light. Give the mechanism of the reaction of bromine with Q: you may represent the compound as >C=C< for this purpose of this question. Give the structural formula of the product when Q reacts with potassium dichromate (VI) solution in the presence of dilute sulphuric acid. Describe a test to show that the product formed above is not an aldehyde. Suggest a positive test which would give the identity of the new functional group that is present in the molecule, and state what you would see. The iodine number is a measure of the degree of unsaturation of a molecule. It relates to the number of C=C double bonds in the molecule. It is defined as the number of grams of iodine, I 2, that react with 1.00g of the compound. Show that the iodine number of Q is approximately 3 by calculating the number of grams of iodine, I 2, which reacts with 1.00g of Q. Question 8:Iodine reacts with propanone in the presence of an acid catalyst according to the equation: [CH 3 COCH 3 + I 2 CH 3 COCH 2 I + HI] in presence of acid, H +. data concerning an experiment to determine the rate equation for this reaction are given in the following table: Relative Concentration [CH 3 COCH 3 ] [I 2 ] [H + ] Relative rate 1 1 1 2 1 2 1 2 2 1 1 4 1 1 2 4 State why the rate equation cannot be written from a knowledge only of the chemical equation representing the reaction. Use the data to deduce the order of reaction with respect to (a) propanone ReviewQuestions-G12-Edexcel-Unit-5 Jaydip.Chaudhuri 2

(b) iodine (c) hydrogen ions. What does the order of reaction with respect to iodine tell you about the part that iodine plays in the rate determining step of the reaction? Write the rate equation for the reaction. Use the bond enthalpies given below in kj mol -1, to calculate the enthalpy change for the iodination of propanone. [ C-H, 413; I-I, 151; C-I, 228; H-I, 298]. Draw an enthalpy level diagram for the reaction, showing on it both catalysed and uncatalysed pathways. Question 9:Write an equation to show the reaction that occurs when hydrogen chloride dissolves in water. The following electrode potentials are required in this equation oxidized form reduced form electrode potential (E Ө ) in volts(v) O 2 + 4H + + 4e- 2H 2 O + 1.23 Cl 2 + 2e- 2Cl - 1.36 F 2 + 2e- 2F- 2.87 State and explain what occurs when fluorine is bubbled into water. Write an equation for the expected reaction of chlorine with water using above data. In fact the reaction between chlorine and water is usually represented by the equation. [Cl 2 + H 2 O H + + Cl - +HOCl]. Suggest why this reaction occurs rather than the one you suggested before. Write an equation to show the disproportion of the chlorate(i) ion in solution and give the conditions necessary for this to occur. Use the equation to explain the word disproportion. When solid KBrO 3 is heated, oxygen is evolved, and a white solid remains, if the white solid is dissolved in water and aqueous silver nitrate is added, a cream precipitate is formed which is soluble in concentrated ammonia solution. Suggest the name of the white solid and write an ionic equation for the reaction that occurs on the addition of the aqueous silver nitrate. Hence write an equation to represent the thermal decomposition of KBrO 3. KIO 3 reacts with hydrogen peroxide according to the equation [2IO - 3 + 2H + + 5H 2 O 2 I 2 + 6H 2 O + 5O 2 ] deduce the ionic half equations for the reduction and oxidation reaction. What would be seen if the reagents were mixed in a conical flask. Question 10:Consider the following reaction scheme Compound D and E have the same functional group. Identify using structural formula, the compound B and C, and the functional group in both D and E. Give the reagent and conditions necessary for the conversion of the compound C into D. Give an equation to represent the reaction that takes place when compound C is boiled with dilute hydrochloric acid. State the type of reaction taking place above. What structural feature of the group present in both D and E enables them each to react with dilute hydrochloric acid? Using the structural formula, give an equation to represent the reaction of compound D with dilute HCl. A compound c6h7n, having the same functional group as D and E reacts with nitrous acid in presence of hydrochloric acid. The resulting solution reacts with alkaline 2- napthol to give a red precipitate. Give the equation representing c6h7n with nitrous acid, using structural formulae. Show the structure of the product which is formed with 2-napthol. What is the significance of compound of this type? Question 11:The kinetics of a reaction are used to clarify reaction mechanism. An experiment to determine the kinetics of substitution reaction between 2-chloro-2-methyl propane and sodium hydroxide used equal initial concentrations of these substances in aqueous ethanol solvent. A mixture ReviewQuestions-G12-Edexcel-Unit-5 Jaydip.Chaudhuri 3

was maintained at 25 O C, and samples were taken at intervals. The samples were quenched in about twice their volume of cold propanone, and the concentration of sodium hydroxide was found time in min 0 7 15 27 44 60 concentration in mol dm -3 0.080 0.065 0.054 0.041 0.028 0.020 Show, by means of a suitable graph, that the reaction is first order. As performed, the results cannot distinguish between the rate laws (rate= k [OH - ] and rate = k [halogenoalkane] ). Outline a further experiment which must be performed to enable the distinction to be made, showing how the new data would be used to establish the rate law. The reaction is, in fact, first order with respect to the halogenoalkane. Write the mechanism for the substitution reaction, identifying the rate determining step. Nucleophilic substitution is usually accompanied by elimination as a competing reaction. Write the name and structural formula of the product of the elimination reaction with 2 chloro-2-methyl propane and state the conditions which favour elimination over substitution. Question 12:Consider the following reaction scheme in which all of the compounds have straight chain. Give the structural formula of A. state the conditions under which the reaction in step 1 is carried out. After giving consideration to the sequence of reactions in step 2, 3 and 4 (a) write the structural formula of c4h8o. (b) write the structural formula of B. (c) identify the yellow precipitate D formed in step 4. (d) give the structural formula of E (e) give the structural formula of C. the mass spectrum and infrared spectrum of C are shown below Explain how the infra-red spectrum is consistent with the identity of C. Question 13:An oily liquid Z can be produced from propanone by the following scheme: Write the mechanism for the reaction between propene and hydrogen bromide. Give the names of the reagents and conditions for (a) step 2 and (b) step 3. Step 4 takes place in two stages. Name the reagents for each stage. Give the full structural formula of the liquid Z formed by the reaction of X and Y. ReviewQuestions-G12-Edexcel-Unit-5 Jaydip.Chaudhuri 4

Question 14:Bullet proof vests are made from Kevlar. The first step in its manufacture is the polymerisation of two monomers benzene-1.4-diamine and benzene-1,4-dicarboxylic acid. Draw the structural formula of the polymer showing one repeating unit. The infrared spectrum of one of the monomers is given below together with date from some common IR absorption wave number ranges. Use the data to assign the bonds which cause the peak A and B and hence identify which of the monomers produces this spectrum. Benzene-1,4-dicarboxylic acid can be made in laboratory by heating 1,4-dimethyl benzene (boiling temperature 138 O C) under reflux for 1½ hours with an alkaline solution of potassium manganate(vii). Potassium manganate (VII) is reduced to a brown precipitate of manganese (IV) oxide. Concentrated hydrochloric acid is carefully added until the brown ppt disappears. The mixture is cooled and the benzene-1,4-dicarboxylic acid is filtered off and recrystallised from boiling water. Why is it necessary to have reflux condenser in this preparation? Why must the solution be cooled before filtering? The purity of the product was tested by observing its melting temperature. What would be noticed if the sample were still impure? Poly(1,1-difluoro ethane) PDFE is a piezoelectric substance. This means that when it is physically deformed, it produces an electric current. Draw the structure of the polymer showing two repeating unit. Name the different types of polymerisation involved in the manufacture of Kevler and PDFE. Propane and octane are both used as fuels in car engine. 1.00g of propane (BP is -42 O C) produces 2.99g of carbon dioxide and 50.4 kj of energy when burnt. 1.00g of octane (BP is + 126 O C) produces 3.09g of carbon dioxide and 48.4 kj of energy when burnt. Give one environmental disadvantage of using octane rather than using propane as a fuel. Stating clearly why its use is more harmful. Suggest one disadvantage of using propane over octane in a car engine. Question 15: Butenedioic acid has the structure [HOOC-CH=CH-COOH]. It has two geometric isomers cis and trans-butenedioic acid. Explain in terms of orbitals why butenedioic acid has geometric isomers. The following concerns cis-butenedioic acid (a) draw the structure of the compound formed when cis butenedioic acid reacts with bromine dissolved in an organic solvent. (b) On heating to 145 O C, cis- butenedioic acid loses water to form a compound containing a five member ring which includes one oxygen atom [C 4 H 4 O 4 C 4 H 2 O 3 + H 2 O]. Draw the structural formula of C 4 H 2 O 3. Draw the structure of trans- butenedioic acid. Suggest why trans- butenedioic acid does not lose water at 145 O C. if cis butenedioic acid is reduced with lithium Aluminium hydride, LiAlH 4, the product is cis-but-2-ene-1,4-diol [HOCH 2 -CH=CH-CH 2 OH]. State the conditions for the reaction between LiAlH 4 and cis- butenedioic acid. How would you test for the presence of the hydroxyl group, and what would you see as a result of your test? If cis-but-2-ene-1,4-diol reacts with compound ClCHCH 2 COCl, a polymer results. Draw enough of the chain of this polymer to make its repeating structure clear. Suggest why the polymer would not be suitable for use in strongly alkaline or acidic conditions. ReviewQuestions-G12-Edexcel-Unit-5 Jaydip.Chaudhuri 5