ocr b f334 specification points

Upload: sahibzada-iqbal

Post on 20-Feb-2018

230 views

Category:

Documents


0 download

TRANSCRIPT

  • 7/24/2019 OCR B F334 Specification Points

    1/21

    Dr A. Johnston, Southampton, 2014

    A2 Unit F334: Chemistry of Materials

    Topic 1: Whats in a medicine? (WM)

    A study of medicines such as aspirin, their development, chemistry and synthesis, illustrating some of the features of the pharmaceutical industry.

    The chemical ideas in this module are:

    Phenols, carboxylic acids, esters, carbonyl compounds.

    Acidbase reactions. Medicine manufacture and testing.

    IR spectroscopy and mass spectroscopy.

    Topic AS code Number Assessable learning outcomesNumber of

    questions

    CGP-A2

    Revision guide

    (Page number)

    Chemical

    storylines

    (Page number)

    Chemical ideas

    (Page number)

    Equilibria

    WM1i

    Describe acids in terms of the BrnstedLowry

    theory as proton donors, and bases as proton

    acceptors.

    5 4 180

    WM1ii Identify the proton donor and proton acceptor in anacidbase reaction. 5 4 180

    Bonding and

    structure EL13i WM2

    Draw andinterpretsimple electron dot-and-cross

    diagrams to show how atoms bond through ionic,

    covalent and dative covalent bonds.

    2 5-6 36-37

    EL13iii WM3 Describe a simple model of metallic bonding. 5 41

    EL15 WM4

    Use the electron pair repulsion principle to predict

    and explain the shapes of simple molecules (such as

    CH4, NH3, H2O and SF6) and ions (such as NH4+) with

    up to six outer pairs of electrons. (any combination

    of bonding pairs and lone pairs) (no treatment ofhybridisation or molecular orbitals is expected).

    1 7 44-46

  • 7/24/2019 OCR B F334 Specification Points

    2/21

    Dr A. Johnston, Southampton, 2014

    EL14 WM5

    Recall the typical physical properties (melting point,

    solubility in water, ability to conduct electricity)

    characteristic of giant lattice (metallic, ionic,

    covalent network) and simple molecular structure

    types (synoptic).

    6 117

    Organic

    functional

    groups

    WM6iRecogniseandwriteformulae for members of the

    following homologous series: diols.1 8

    WM6iiRecogniseandwriteformulae for members of the

    following homologous series: diamines. 28

    WM6iiiRecogniseandwriteformulae for members of the

    following homologous series: dicarboxylic acids10

    WM6ivRecogniseandwriteformulae for members of the

    following homologous series:phenols.2 12 280, 303-304

    WM6vRecogniseandwriteformulae for members of the

    following homologous series: acyl chlorides.13 339-340

    WM6viRecogniseandwriteformulae for members of the

    following homologous series: acid anhydrides.340-341

    WM6viiRecogniseandwriteformulae for members of the

    following homologous series: esters. 6 10 307-311

    WM7iUse systematic nomenclature to name and interpret

    the names of diols.8

    PR5iii WM7iiUse systematic nomenclature to name and interpret

    the names of carboxylic acids.1 10

    WM7iiiUse systematic nomenclature to name and interpret

    the names of dicarboxylic acids.10

    PR5i WM7ivUse systematic nomenclature to name and interpret

    the names of aldehydes.1 14 316

    PR5ii WM7v Use systematic nomenclature to name and interpretthe names of ketones. 14 316

    WM7vi

    Use systematic nomenclature to name and interpret

    the names of other organic compounds whose

    naming was required in the AS course (synoptic).

    4 8

  • 7/24/2019 OCR B F334 Specification Points

    3/21

    Dr A. Johnston, Southampton, 2014

    ES21,

    ES23iiiWM8i

    Recall the reactions (as described in the modules

    named) of halogenoalkanes(ES).9 288-294

    PR10i-

    PR10iiiWM8ii

    Recall the reactions (as described in the modules

    named) ofalkenes(PR).9 272-277

    PR11i-

    PR11iiiWM8iii

    Recall the reactions (as described in the modules

    named) of alcohols (PR) (synoptic).3 9 317

    WM9

    Describe and explain the acidic nature of carboxylic

    acids, and their reaction with alkalis and carbonates.

    Drawa carboxylate ion and describeits properties.

    4 10 317

    WM10

    Describe the reaction of alcohols with carboxylic

    acids in the presence of concentrated sulfuric acid or

    concentrated hydrochloric acid to form esters.

    5 10 305

    WM11i

    Describethe following properties of phenols: acidic

    nature, and their reaction with alkalis but not

    carbonates.

    5 12 304

    WM11ii

    Describethe following properties of phenols: test

    with neutral iron(III) chloride solution, to give a

    purple colouration.

    3 12 304

    WM11iiiDescribethe following properties of phenols:

    reaction with acyl chlorides to form esters.1 13 309

    WM12i

    Describe the following reactions involving carbonyl

    compounds (aldehydes and ketones): formation of

    carbonyl compounds by oxidation of alcohols using

    acidified dichromate with the need to distil in the

    case of aldehydes (synoptic).

    14 318

    WM12ii

    Describe the following reactions involving carbonyl

    compounds (aldehydes and ketones): the oxidation

    of aldehydes to carboxylic acids using acidified

    dichromate, under reflux.

    1 14 318

    WM12iii

    Describe the following reactions involving carbonyl

    compounds (aldehydes and ketones): reaction with

    hydrogen cyanide to form the cyanohydrin.

    3 15 319

  • 7/24/2019 OCR B F334 Specification Points

    4/21

    Dr A. Johnston, Southampton, 2014

    WM13

    Describethe techniques for heating and purifying

    volatile liquids: heating under reflux and distillation

    (synoptic).

    2 14 367-368

    WM13

    Describe the mechanism of the nucleophilic addition

    reaction between a carbonyl compound and

    hydrogen cyanide, using curly arrows and bond

    polarities.

    3 15 319

    Reaction

    mechanisms WM14

    Understandthat more effective medicines can be

    obtained by modifying the structure of existing

    medicines.

    18 8-11

    WM15

    Discuss given examples and understandthat

    combinatorial chemistry is used to make a large

    number of related compounds together, so that

    their potential effectiveness as medicines can be

    assessed by large-scale screening.

    18 159

    ES14i WM16iRecall the meaning of the concept atom economy

    (synoptic).1 16-17 334

    WM16ii

    Understand that most reactions used in chemical

    synthesis can be classified as: rearrangement,

    addition, substitution, elimination.

    1 16 360

    WM16iiiUnderstand that a condensation reaction is addition

    followed by elimination.2 16 110

    WM16iv

    Recall andUnderstand that rearrangement and

    addition reactions have a higher atom economy than

    substitution and condensation reactions, which have

    a higher atom economy than elimination reactions.

    3 16-17 360-361

    WM16v

    Discuss the importance of atom economy and

    reaction type in working towards the development

    of environmentally friendly industrial processes in

    the production of polymers and medicines.

    6 19 362-364

  • 7/24/2019 OCR B F334 Specification Points

    5/21

    Dr A. Johnston, Southampton, 2014

    WM17

    Understandthat testing a medicine involves clinical

    trials which answer the following questions about a

    potential new drug:

    Step IIs it safe?

    Step IIDoes it work?

    Step IIIIs it better than the standard treatment?

    2 18-19 13-15 -

    WM18i

    Describe the technique of thin-layer

    chromatography (TLC), including location of spots

    using iodine or ultraviolet radiation, and interpret

    results in terms of number of spots and matching

    heights or Rf values with known compounds.

    1 21 176-177, 369

    Modern

    analytical

    techniques

    WM18iiUnderstand that chromatography can be used for

    the purification of an organic substance.21-22, 45 178

    EL21ii WM19iInterpret and predict mass spectra: identifythe M+

    peak and explain that it indicates the Mr (synoptic).23-25 6-7 139-146

    WM19ii

    Interpret and predict mass spectra: explain how the

    molecular formula can be worked out from the high-

    resolution value of the M+peak.

    1 23-25 6-7 139-146

    EL21iii WM19iii

    Interpret and predict mass spectra: recall that other

    peaks are due to positive ions from fragments and

    the mass differences between peaks.

    2 23-25 6-7 139-146

    WM19iv

    Interpret and predict mass spectra: suggestthe

    origins of peaks, e.g. peaks at masses of 15 and 77

    are usually due to the presence of the methyl and

    phenyl positive ions.

    1 23-25 6-7 139-146

    WM19v

    Interpret and predict mass spectra: indicate the loss

    of groups of atoms, e.g. loss of a methyl group would

    be indicated by a mass difference of 15.

    3 23-25 6-7 139-146

    WM20i

    Use information given in the Data Sheet tointerpret

    andpredictinfrared spectra for organic compounds,

    in terms of the functional group(s) present.

    8 20 5 132-139

    WM20iiUnderstand that specific frequencies of infrared

    radiation make specific bonds vibrate more.20 5 132-139

  • 7/24/2019 OCR B F334 Specification Points

    6/21

    Dr A. Johnston, Southampton, 2014

  • 7/24/2019 OCR B F334 Specification Points

    7/21

    Dr A. Johnston, Southampton, 2014

    Unit 2: The Materials Revolution (MR)

    A study of condensation polymers and other modern materials.

    The chemical ideas in this module are:

    Condensation polymers.

    Amines and amides.

    Factors affecting the properties of polymers.

    Disposal of polymers.

    Topic AS Code Number Assessable learning outcomesNumber of

    questions

    CGP-A2

    Revision guide

    (Page number)

    Chemical

    storylines

    (Page number)

    Chemical ideas

    (Page number)

    Bonding and

    structure

    ES6 MR1i Explain the term electronegativity. 1 26-27 40-41

    MR1iiRecall qualitatively the electronegativity trends in the

    Periodic Table.26-27 40-41

    MR1iiiUse relative electronegativity values to predict bond

    polarity in a covalent bond.97

    MR1iv

    Decide whether a molecule is polar or nonpolar from

    its shape and the polarity of its bonds. 27

    ES7i MR2i

    Explain, give examples of and recognise in given

    examples the following types of intermolecular bonds:

    instantaneous dipoleinduced dipole bonds (including

    dependence on branching and chain length of organic

    molecules).

    3 27 93-98

    ES7ii MR2ii

    Explain, give examples of and recognise in given

    examples the following types of intermolecular bonds:

    permanent dipolepermanent dipole bonds.

    2 27 93-98

    PR1i MR2iii

    Explain, give examples of and recognise in given

    examples the following types of intermolecular bonds:

    hydrogen bonds (synoptic).

    2 27 93-98

  • 7/24/2019 OCR B F334 Specification Points

    8/21

    Dr A. Johnston, Southampton, 2014

    MR3i

    Explain and predict the effect of temperature on the

    properties of polymers: intermolecular bonds have

    more effect as the temperature is lowered; a polymer

    softens above its Tmand becomes brittle below its Tg.

    3 34 111

    MR3ii

    Explain and predict the effect of crystallinity on the

    properties of polymers: (regular packing of the chains,

    due to the regular structure of the polymer)the

    chains are closer and the intermolecular bonds have

    more effect, leading to greater strength.

    6 34 107-108

    MR3iii

    Explain and predict the effect of chain length on the

    properties of polymers: there are more intermolecular

    bonds leading to greater strength.

    34 112

    MR3iv

    Explain and predict the effect of chain length on the

    properties of polymers: explain that flexibility depends

    on the ability of the polymer chains to slide over each

    other.

    1 34 107-108

    MR4

    Explain the following ways that chemists can modify

    the properties of a polymer to meet particular needs:

    cold drawing to make the structure more crystalline,

    copolymerisation and the use of plasticisers.

    3 35 113

    MR5

    Understand that the properties of all materials depend

    on their structure and bonding andexplain examples

    given relevant information.

    1 34-35 113

    Organicfunctionalgroups

    MR6iRecognise members of the following homologous

    series: amines.2 28 320

    MR6iiRecognise members of the following homologous

    series: amides.6 29 323

    MR7

    Use systematic nomenclature to name and interpret

    the names of aliphatic primary amines and diamines

    (use the prefix amino- for the NH2group together with

    the parent hydrocarbon, e.g. 2-aminopropane, 1,6-

    diaminohexane).

    4 28 320

  • 7/24/2019 OCR B F334 Specification Points

    9/21

    Dr A. Johnston, Southampton, 2014

    Organic

    reactionsMR8

    Explain the difference between additionand

    condensationpolymerisation.1 31

    107, 110, 324-

    325

    MR9

    Predict the structural formula of the condensation &

    addition polymers formed from given monomer(s), and

    vice versa.

    10 31-32 19-20 107,110

    MR10

    Describe the hydrolysis of esters and amides by both

    aqueous acids and alkalis, including salt formation

    where appropriate.

    3 29

    309-310

    (esters)

    323-324

    (amides)

    MR11Describe the following reactions of amines:

    neutralisation by acids, acylation to form an amide.1 19 322-323

    MR12i

    Recall the procedure for purifying an organic solid

    product by recrystallisation, and explain that the

    solvent used must be one in which the substance is

    very soluble at higher temperatures and insoluble, or

    nearly so, at lower temperatures.

    2 30 369-370

    MR12ii

    Recall the procedure for purifying an organic solid

    product by recrystallisation, and explain that the

    solvent used is saturated by the substance at higher

    temperatures, and on cooling the substance then

    crystallises out, to leave the impurities in solution.

    2 30 369-370

    Reaction

    mechanisms MR13

    Explain the basic nature of the amino group, in terms

    of a lone pair on the nitrogen accepting a proton to give

    a cation.

    2 28 321

    Applications

    MR14i

    Understandhow the principles of green chemistry are

    important in the manufacture, use, recycling and the

    eventual disposal of polymers, including: minimising

    any hazardous waste during production of raw

    materials and their resulting polymers to reduce any

    negative impact on the environment.

    3 32-33 26 364-366

  • 7/24/2019 OCR B F334 Specification Points

    10/21

    Dr A. Johnston, Southampton, 2014

    MR14ii

    Understandhow the principles of green chemistry are

    important in the manufacture, use, recycling and the

    eventual disposal of polymers, including: reducing

    carbon emissions resulting from the life cycle of a

    polymer.

    32-33 364-366

    MR14iii

    Understandhow the principles of green chemistry are

    important in the manufacture, use, recycling and the

    eventual disposal of polymers, including: recycling to

    produce energy and chemical feedstocks.

    32-33 364-366

  • 7/24/2019 OCR B F334 Specification Points

    11/21

    Dr A. Johnston, Southampton, 2014

    Unit 3: The thread of life (TL)

    A study of proteins and enzymes. DNA and its use in synthesising proteins.

    The chemical ideas in this module are:

    rates of reaction;

    enzymecatalysis;

    optical isomerism;

    amino acid and protein chemistry;

    the structure and function of DNA.

    Topic AS Code Number Assessable learning outcomesNumber of

    questions

    CGP-A2

    Revision guide

    (Page number)

    Chemical

    storylines

    (Page number)

    Chemical ideas

    (Page number)

    Kinetics TL1i Explain and use the terms: rate constant, including units. 2 39

    TL1ii Explain and use the terms: rate of reaction. 36 210

    TL1iiiExplain and use the terms: order of reaction(both

    overall and with respect to a given reagent)38 219-220

    TL2iUse empirical rate equations of the form: rate =

    k[A]m[B]nwhere m and n are integers. 2 38

    TL2ii Carry out calculations based on the rate equation. 1 37-41 225

    TL2iiiUnderstand that the rate constant k increases with

    increasing temperature.1 38 221

    TL2ivDescribe of the concentration of reactants affects the

    rate of reaction.

    TL3i

    Understand that these experimental methods can be

    used in a school laboratory for following a reaction:

    titration.

    2 36

    TL3ii

    Understand that these experimental methods can be

    used in a school laboratory for following a reaction:

    colorimetry.

    4 36 224

    TL3iii

    Understand that these experimental methods can be

    used in a school laboratory for following a reaction:

    measuring volumes of gases evolved.

    2 36 216-217

  • 7/24/2019 OCR B F334 Specification Points

    12/21

    Dr A. Johnston, Southampton, 2014

    TL3iv

    Understand that these experimental methods can be

    used in a school laboratory for following a reaction: pH

    measurement.

    1 36

    TL3v

    Understand that these experimental methods can be

    used in a school laboratory for following a reaction:

    measuring mass changes.

    1 36 217

    TL4i Design experiments to calculate the rate of reaction. 2 36 216-225

    TL4ii Calculate the rate of the reaction. 2 36 216-225

    TL5 Use given data to calculate half-lives for a reaction. 1 40-41 221-228

    TL6

    Use experimental data (half-lives or initial rates when

    varying concentrations are used) to find the order of a

    reaction (zero-, first- or second-order), and hence

    constructa rate equation for the reaction.

    5 40-41, 44 223-228

    TL7Use the term rate-determining step to describe the

    slowest step in a reaction.2 42 225

    TL8i

    Explain the shape of the rate versus substrate

    concentration curve for an enzyme-catalysed reaction in

    terms of the rate-determining step: at low

    concentrations of substrate the order with respect to the

    substrate is one.

    2 43 230-231

    TL8ii

    Explain the shape of the rate versus substrate

    concentration curve for an enzyme-catalysed reaction in

    terms of the rate-determining step: at higher

    concentrations of substrate the order with respect to the

    substrate is zero.

    1 43 230-231

    TL8iii

    Explain, given the necessary data, the useful information

    about the mechanism of a reaction that can be obtained

    from the rate-determining step.

    1 42-43 225-228

    Organic

    functional

    groups

    TL9

    Recognise and describe the generalised structure of

    amino acids and recall that proteins are condensation

    polymers formed from amino acid monomers.

    5 45-46 38 326

    TL10iDescribe the primary, secondary and tertiary structure of

    proteins.1 46 39-40 328

  • 7/24/2019 OCR B F334 Specification Points

    13/21

    Dr A. Johnston, Southampton, 2014

    TL10ii

    Explain the importance of amino acid sequence in

    determining the properties of proteins, and account for

    the diversity of proteins in living things.

    46 36-40

    TL11

    Explain the role of hydrogen bonds and other

    intermolecular bonds in determining the secondary and

    tertiary structures, and hence the properties of proteins.

    1 47 39-40 328

    Organicreactions

    TL12 Describe the acidbase properties of amino acids. 1 45 326

    TL13

    Recall that amino acids usually exist as zwitterions. and

    describetheir properties. 3 45 326

    TL14iDescribe the formation and hydrolysis of the peptide link

    between amino acid residues in proteins.1 329

    TL14ii

    Describe the use of paper chromatography to identify

    amino acids, including the need for a suitable locating

    agent, such as ninhydrin.

    45 369

    TL15iDescribe the characteristics of enzyme catalysis,

    including:temperature sensitivity.3 54 44

    TL15iiDescribe the characteristics of enzyme catalysis,

    including: specificity.54 42

    TL15iiiDescribe the characteristics of enzyme catalysis,

    including:inhibition.55 43

    TL15ivDescribe the characteristics of enzyme catalysis,

    including:pH sensitivity.1 54 41-45

    TL16i

    Explain these characteristics of enzyme catalysis in terms

    of a three-dimensional active site (part of the tertiary

    structure) to which the substrate forms intermolecular

    bonds.

    3 54 41-45

    TL16iiRecall that molecules acting as inhibitors bind to active

    sites but do not react.55 41-45 230

    TL17

    Understand that DNA is a condensation polymer formed

    from nucleotides, which are monomers having three

    components: phosphate, sugar and base.

    1 48 46-49

  • 7/24/2019 OCR B F334 Specification Points

    14/21

    Dr A. Johnston, Southampton, 2014

    TL18

    Explain, using the structures on the Data Sheet, how:

    phosphate units join by condensation with deoxyribose

    to form the phosphatesugar backbone in DNA.

    1 48 46-49

    TL19i

    Explain, using the structures on the Data Sheet, how: the

    four bases present in DNA join by condensation with the

    deoxyribose in the phosphate sugar backbone.

    1 48 46-49

    TL19ii

    Explain, using the structures on the Data Sheet, how:

    two strands of DNA form a double-helix structure

    through base pairing.

    2 49 46-49

    TL19iiiUnderstand that various models were devised before

    the currently accepted version was formulated.2 48

    TL20

    Using the structures on the Data Sheet, describe and

    explain the significance of hydrogen bonding in the

    pairing of bases in DNA, and relate to the replication of

    genetic information.

    2 50 49

    TL21Use the diagram on the Data Sheetto explainhow DNA

    encodes for an amino acid sequence in a protein.2 52-53 50-52

    Isomerism

    DF19 TL22

    Draw andinterpretstructural formulae (full, shortened

    and skeletal).

    DF20 TL23i

    Use the concept of repulsion of areas of electron density

    to deducethe bond angles in organic molecules

    (including double bonds, no treatment of small deviation

    of angle due to lone pair repulsion required)

    56 269, 273

    DF21 TL23iiRelate molecular shape to structural formulae and use

    wedges and dotted lines to represent 3D shape.1 56-57 44

    DF23 TL23iii Recognise anddraw structural isomers. 56 47-50

    PR13i TL23iv

    Recognise where E/Zisomerism occurs, explaining it in

    terms of lack of free rotation about C=C bonds when

    there are two different groups on each carbon.

    4 56 50-51

  • 7/24/2019 OCR B F334 Specification Points

    15/21

    Dr A. Johnston, Southampton, 2014

    PR13ii TL23v

    Draw andinterpret diagrams to represent E/Z isomers

    for alkenes which have the same groups on both sides of

    the double bond (Eopposite sides of bond; Zsame

    side of bond); in such molecules, describe E as trans

    and Z as cis and extend this cistrans nomenclature to

    other, more complicated, alkenes (synoptic) (knowledge

    of CahnIngoldPrelog priority rules will not be required)

    56 50-51

    TL24i

    Draw andinterpret diagrams to represent optical

    stereoisomers of molecules. 1 57 52-54

    TL24ii Explain and usethe term chiral as applied to a molecule. 7 57 52-54

    TL24iiiExplainthat enantiomers are non-superimposable mirror

    image molecules.4 57 52-54

    ApplicationsTL25

    Understandthat DNA analysis can be used for genetic

    fingerprinting.1 51 53-54

    TL26Discuss the ethical issues of using and storing data from

    human DNA analysis, given examples.1 51 53-54

    TL27

    Givenexamples, understandthe industrial importance

    of enzymes and of their contribution to green chemistry

    processes.

    53 363-364

  • 7/24/2019 OCR B F334 Specification Points

    16/21

    Dr A. Johnston, Southampton, 2014

    Unit 4: The Steel Story (SS)

    An account of the production, properties and uses of steel, with reference to other metals.

    The chemical ideas in this module are:

    Redox reactions.

    Electrode potentials.

    d-block chemistry.

    Colorimetry.

    TopicAS

    CodeNumber Assessable learning outcomes

    Number of

    questions

    CGP-A2

    Revision guide

    (Page number)

    Chemical

    storylines

    (Page number)

    Chemical ideas

    (Page number)

    Formulae,

    equations

    and

    amount of

    substance

    SS1iUse the concept of amount of substance to calculate

    molecular formulae.

    ES1ii SS1iiUse the concept of amount of substance to calculate

    percentage yields.357-358

    DF1i SS1iiiUse the concept of amount of substance to calculate

    volumes of gases.

    10-11

    ES1v SS1ivUse the concept of amount of substance to calculate

    volumes of solutions of known concentrations.2 12-13

    SS1vUse the concept of amount of substance to calculate

    balanced chemical equations (synoptic).

    ES1iii SS1vi

    Use the concept of amount of substance to calculate

    amount of substance to calculate mass/amount of

    reactant or product.

    59 8

    EL1iii SS2iWrite andinterpret balanced equations, given the

    necessary information (synoptic).5 7

    ES1vii SS2ii Write andinterpret balanced ionic equations given thenecessary information (synoptic).

    5 85, 250

    ES2 SS3

    Given the necessary information,describe andexplain

    procedures for acidbase (synoptic) and redox titrations

    and carry out non-structured calculations based on the

    results.

    7 59

  • 7/24/2019 OCR B F334 Specification Points

    17/21

    Dr A. Johnston, Southampton, 2014

    Bonding and

    structure

    SS4i Use andexplain the term coordination number. 2 68-69 258-260

    SS4ii

    Draw andname the shapes of complexes with

    coordination numbers 4 (square planar and tetrahedral)

    and 6 (octahedral).

    3 68-69 258-259

    Redox

    SS5i

    Given the necessary information,describe redox reactions

    of d-block elements (and main group elementssynoptic)

    in terms of electron transfer.

    1 60 193-194

    SS5ii

    Given the necessary information,describe redox reactions

    of d-block elements assigning oxidation states. 5 60 194-197

    SS5iii

    Given the necessary information,describe redox reactions

    of d-block elements using half-equations to represent the

    oxidation and reduction reactions (synoptic).

    2 61 198-199

    SS5iv

    Given the necessary information,describe redox reactions

    of d-block elements combining half equations to give the

    overall equation for the reaction.

    5 60-61 199

    SS5v

    Given the necessary information,describe redox reactions

    of d-block elements recognising the oxidising and

    reducing agents.

    8 60-61 198-199

    SS5vi

    Given the necessary information,describe redox reactions

    of d-block elements defining oxidation and reduction in

    terms of loss and gain of electrons.

    2 60-61 198-199

    SS6

    Usesystematic nomenclature to nameand interpretthe

    names of inorganic compounds [ie copper(II) sulfide,

    lead(II) nitrate(V), potassium manganate(VII), not complex

    ions]

    1 196-197

    SS7Recalland explainthe procedure for carrying out a redox

    titration involving manganate(VII) ions.59

    SS8i

    Describethe construction of simple electrochemical cells

    involving: metal ion/metal half-cells. 1 62 199-204

    SS8ii

    Describethe construction of simple electrochemical cells

    involving: half-cells based on different oxidation states of

    the same element in aqueous solution with a platinum or

    other inert electrode.

    1 62 199-204

  • 7/24/2019 OCR B F334 Specification Points

    18/21

    Dr A. Johnston, Southampton, 2014

    SS8iiiDescribethe construction of simple electrochemical cells,

    involving acidified cells.62 199-204

    SS9i

    Explainand use the term standard electrode potential and

    understandhow a standard electrode potential is

    measured using a hydrogen electrode (details of electrode

    not required).

    62 199-204

    SS9iiExplain the action of an electrochemical cell in terms of

    half-equations and external electron flow.62 199-204

    SS10i Usestandard electrode potentials to calculateEcell. 3 63 203-204

    SS10iiUsestandard electrode potentials to predict the feasibility

    of redox reactions.4 63 206-208

    SS10iii

    Understand that the rate of reaction may be an important

    factor in deciding whether the reaction actually takes

    place under standard conditions.

    208

    SS11

    Describerusting in terms of electrochemical processes

    involving iron, oxygen and water, and the subsequent

    reactions to form rust.

    64-65 204

    SS12i

    Describeandexplain approaches to corrosion prevention:

    sacrificial protection by galvanising and use of zinc blocks. 64-65

    SS12ii

    Describeandexplain approaches to corrosion prevention:

    barrier protection using oil, grease, paint or a polymer

    coating.

    64-65 67-68

    SS13i

    Describe andexplain the issues involved in the recycling

    of iron and steel: all steel packaging except aerosols can

    be recycled.

    64-65 69-70

    SS13iiDescribe andexplain the issues involved in the recycling

    of iron and steel: cleaning by incineration.64-65

    SS13iii

    Describe andexplain the issues involved in the recycling

    of iron and steel: ease of sorting using magnetic

    properties.

    64-65

    SS13iv

    Describe andexplain the issues involved in the recycling

    of iron and steel: composition of new steel easily

    adjusted.

    64-65

  • 7/24/2019 OCR B F334 Specification Points

    19/21

    Dr A. Johnston, Southampton, 2014

    SS13v

    Describe andexplain the issues involved in the recycling

    of iron and steel: scrap is used to adjust temperature of

    furnace.

    64-65

    Inorganic

    chemistry

    and the

    Periodic

    Table

    SS14

    Given the necessary information,explain the chemical

    processes occurring during the extraction and purification

    of metals from their ores.

    1 65 59-63

    EL16i SS15i

    Recall that the Periodic Table lists elements in order of

    atomic (proton) number and groups elements together

    according to their common properties.

    66

    ES11ii SS15iiRecall the classification of elements into s-, p- and d-

    blocks.66 26-30

    ES11iii SS15iii

    Recall and explain the relationship between the position

    of an element in the Periodic Table and the charge on its

    ion.

    66 33-35

    ES11iv SS15ivRecall the names and formulae of NO3, SO42, CO32, OH,

    NH4+, HCO3-.2 70

    SS15vWrite formulae for compounds formed between these

    ions and other given anions and cations (synoptic).6

    SS16i

    Recall that transition metals are d-block elements forming

    one or more stable ions which have incompletely filled d-

    orbitals.

    1 66 251-253

    SS16iiRecall the common oxidation states of iron and copper

    and the colours of their aqueous ions.2 67

    SS17i

    Describe the colour changes in and write ionic equations

    for the reactions of: Fe2+(aq), Fe3+(aq) and Cu2+(aq) ions

    with sodium hydroxide solution.

    3 70

    SS17iiDescribe the colour changes in and write ionic equations

    for the reactions of: Cu2+(aq) ions with ammonia solution.70

    ES3 SS18

    Use conventions for representing the distribution of

    electrons in atomic orbitals (no treatment of the shapes of

    atomic orbitals is expected).

    66 252

  • 7/24/2019 OCR B F334 Specification Points

    20/21

    Dr A. Johnston, Southampton, 2014

    ES4 SS19i

    Write out the electronic configuration, using sub-shells

    and atomic orbitals, for atoms and ions of the first row of

    the d-block elements (and the main group elements up to

    kryptonsynoptic).

    4 66 252

    SS19ii

    Use the electronic configuration, using sub-shells and

    atomic orbitals, for atoms and ions of the first row of the

    d-block elementstoexplain the existence of variable

    oxidation states, in terms of the stability of d orbital

    electron arrangements.

    71 255-256

    SS20i

    Explain the catalytic activity of transition metals and their

    compounds: homogeneous catalysis in terms of variable

    oxidation states.

    4 71 256-257

    SS20ii

    Explain the catalytic activity of transition metals and their

    compounds: heterogeneous catalysis in terms of the

    ability of transition metals to use (3)d and (4)s electrons of

    the atoms on the catalyst surface to form weak bonds to

    reactants.

    1 71 256-257

    SS21i Explain anduse the terms: ligand. 1 68 258-261

    SS21ii Explain anduse the terms: complex/complex ion. 68 258-261

    SS21iii Explain anduse the terms: ligand substitution. 68 258-261

    SS22

    Recall the formulae of the following examples of complex

    ions from the chemistry of: iron: [Fe(H2O)6]2+, [Fe(H2O)6]3+;

    copper: [Cu(H2O)6]2+, [Cu(NH3)4]2+, [CuCl4]2-.

    3 68 261

    SS23

    Describe the formation of complexes in terms of

    coordinate (dative) bonding betweenligand and central

    metal ion.

    2 68 258-261

    SS24Explain the terms bidentate and polydentate as applied to

    ligands, exemplified by ethanedioate and EDTA4.1 68 260-261

    SS25iRecall that the ions of transition metals in solution are

    often coloured.3 72 262-263

  • 7/24/2019 OCR B F334 Specification Points

    21/21

    Dr A. Johnston, Southampton, 2014

    SS25ii

    Explain that this is because they absorb in specific parts of

    the visible spectrum and transmit the complementary

    frequencies (no explanation in terms of energy levels is

    required in this unit)

    2 72 262-263

    SS26i Describe andexplain a simple colorimeter 72-73 372-373

    SS26ii

    Use colorimetric measurements to determine the

    concentration

    of a coloured solution:

    (i) Choose suitable filter/set wavelength.(ii) Make up standard solutions of coloured solution.

    (iii) Zero colorimeter with tube of water/solvent.

    (iv) Measure absorbance of standard solutions.

    (v) Plot calibration curve.

    (vi) Measure absorbance of unknown.

    (vii) Read off concentration from calibration curve.

    4 73 372-373