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<CourseUnit xmlns="http://www.manchester.ac.uk/CUICourseUnitDetails" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.manchester.ac.uk/CUICourseUnitDetails.xsd">
  <UnitCode Applicant="Y" Label="Unit code" Student="Y">
    <Code>CHEM30112</Code>
  </UnitCode>
  <UnitTitle Applicant="Y" Label="Unit title" Student="Y">
    <Title>Personalised Learning Unit 2</Title>
  </UnitTitle>
  <MaxUnits Applicant="Y" Label="Credit rating" Student="Y">
    <Units>10</Units>
  </MaxUnits>
  <TeachingPeriods Applicant="Y" Label="Teaching period(s)" Student="Y">
    <Period>Semester 2</Period>
  </TeachingPeriods>
  <AcademicCareer Applicant="Y" Label="Academic career" Student="Y">
    <Value>Undergraduate</Value>
  </AcademicCareer>
  <UnitLevel Applicant="Y" Label="Unit level" Student="Y">
    <Level>Level 3</Level>
  </UnitLevel>
  <StaffList Applicant="Y" Label="Teaching staff" RoleLabel="Course Unit Role" Student="Y">
    <StaffMember>
      <Name>Andrew Regan</Name>
      <Role>Unit coordinator</Role>
    </StaffMember>
  </StaffList>
  <OfferedBy Applicant="Y" Label="Offered by" Student="Y">
    <OrganisationList>
      <Organisation>
        <OrgName>Department of Chemistry</OrgName>
      </Organisation>
    </OrganisationList>
    <GroupList>
      <Group>
        <GroupName></GroupName>
      </Group>
    </GroupList>
    <FheqLevels>
      <FheqLevel>
        <LevelNumber>1</LevelNumber>
        <LevelName>FHEQ level (Framework for Higher Education Qualifications) ' Last part of a Bachelors ' </LevelName>
      </FheqLevel>
    </FheqLevels>
    <Ects>
      <MaxUnits>European Credit Transfer &amp; Accumulation System Rating :   5.0</MaxUnits>
    </Ects>
  </OfferedBy>
  <MarketingOverview Applicant="Y" Label="Marketing Course unit overview" Student="">
    <Content>&lt;p&gt;This personalised learning unit allows students to choose three (CHEM30112) or four (CHEM60112) advanced chemistry topics. &amp;nbsp;&lt;/p&gt;&lt;p&gt;The over-arching aim of the personalised learning unit is to prepare students for a professional career in Chemistry by expanding core chemistry knowledge into advanced topics, to provide a wider and deeper understanding of particular areas of chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;The key aims of each of the topics are:&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills)&lt;/strong&gt; – This topic introduces students to the use of molecular design to achieve landmark advances in non-aqueous f-element synthetic chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge) &lt;/strong&gt;– This topic introduces students to the catalytic processes that are routinely used for the stereoselective synthesis of target molecules. &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;New topic to be confirmed &amp;nbsp;(J. Abbenseth) &lt;/strong&gt;– &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan)&lt;/strong&gt; – This topic introduces students to the use of silicon-, sulfur- selenium- and phosphorus-containing reagents in organic synthesis.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal-Organic Frameworks (Y. Ma)&lt;/strong&gt; - This topic introduces students to porous metal-organic framework materials.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Chemical Concepts from Quantum Mechanics (P. Popelier) &lt;/strong&gt;– This topic introduces students to Quantum Chemical Topology, the most comprehensive and coherent way of extracting chemical insight from modern wavefunctions.The course will also introduce research-level topics in this area.&amp;nbsp;&lt;/p&gt;</Content>
  </MarketingOverview>
  <UnitOverview Applicant="" Label="Course unit overview" Student="Y">
    <Content>&lt;div style="border:1.0pt solid windowtext;mso-border-alt:solid windowtext .5pt;mso-element:para-border-div;padding:1.0pt 6.0pt 1.0pt 4.0pt;"&gt;&lt;p class="MsoNormal" style="border-style:none;mso-border-alt:solid windowtext .5pt;mso-padding-alt:1.0pt 6.0pt 1.0pt 4.0pt;padding:0cm;"&gt;This personalised learning unit allows students to choose three (CHEM30112) or four (CHEM60112) advanced chemistry topics. &amp;nbsp;&lt;/p&gt;&lt;p class="MsoNormal" style="border-style:none;mso-border-alt:solid windowtext .5pt;mso-padding-alt:1.0pt 6.0pt 1.0pt 4.0pt;padding:0cm;"&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;This personalised learning unit allows students to choose three (CHEM30112) or four (CHEM60112) advanced chemistry topics. &amp;nbsp;&lt;/p&gt;&lt;p&gt;The over-arching aim of the personalised learning unit is to prepare students for a professional career in Chemistry by expanding core chemistry knowledge into advanced topics, to provide a wider and deeper understanding of particular areas of chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;The key aims of each of the topics are:&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills)&lt;/strong&gt; – This topic introduces students to the use of molecular design to achieve landmark advances in non-aqueous f-element synthetic chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge) &lt;/strong&gt;– This topic introduces students to the catalytic processes that are routinely used for the stereoselective synthesis of target molecules. &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;New topic to be confirmed &amp;nbsp;(J. Abbenseth) &lt;/strong&gt;– &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan)&lt;/strong&gt; – This topic introduces students to the use of silicon-, sulfur- selenium- and phosphorus-containing reagents in organic synthesis.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal-Organic Frameworks (Y. Ma)&lt;/strong&gt; - This topic introduces students to porous metal-organic framework materials.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Chemical Concepts from Quantum Mechanics (P. Popelier) &lt;/strong&gt;– This topic introduces students to Quantum Chemical Topology, the most comprehensive and coherent way of extracting chemical insight from modern wavefunctions.The course will also introduce research-level topics in this area.&amp;nbsp;&lt;span style="color:black;"&gt;&lt;span style="font-family:&amp;quot;Microsoft Sans Serif&amp;quot;,sans-serif;font-size:11.0pt;layout-grid-mode:line;"&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;</Content>
  </UnitOverview>
  <Aims Applicant="Y" Label="Aims" Student="Y">
    <Content>&lt;p&gt;The over-arching aim of the personalised learning unit is to prepare students for a professional career in Chemistry by expanding core chemistry knowledge into advanced topics, to provide a wider and deeper understanding of particular areas of chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;The key aims of each of the topics are:&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills)&lt;/strong&gt; – This topic introduces students to the use of molecular design to achieve landmark advances in non-aqueous f-element synthetic chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge)&lt;/strong&gt; – This topic introduces students to the catalytic processes that are routinely used for the stereoselective synthesis of target molecules. &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;New topic to be confirmed &amp;nbsp;(J. Abbenseth) – &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan) &lt;/strong&gt;– This topic introduces students to the use of silicon-, sulfur- selenium- and phosphorus-containing reagents in organic synthesis.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal-Organic Frameworks (Y. Ma)&lt;/strong&gt; - This topic introduces students to porous metal-organic framework materials.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Chemical Concepts from Quantum Mechanics (P. Popelier) &lt;/strong&gt;– This topic introduces students to Quantum Chemical Topology, the most comprehensive and coherent way of extracting chemical insight from modern wavefunctions.The course will also introduce research-level topics in this area.&amp;nbsp;&lt;/p&gt;</Content>
  </Aims>
  <LearningOutcomes Applicant="Y" Label="Learning outcomes" Student="Y">
    <Content>&lt;div class="OutlineElement Ltr SCXW232392082 BCX8" style="-webkit-tap-highlight-color:transparent;-webkit-text-stroke-width:0px;-webkit-user-drag:none;background-color:rgb(255, 255, 255);clear:both;color:rgb(0, 0, 0);cursor:text;direction:ltr;font-family:&amp;quot;Segoe UI&amp;quot;, &amp;quot;Segoe UI Web&amp;quot;, Arial, Verdana, sans-serif;font-size:12px;font-style:normal;font-variant-caps:normal;font-variant-ligatures:normal;font-weight:400;letter-spacing:normal;margin:0px;orphans:2;overflow:visible;padding:0px;position:relative;text-align:start;text-decoration-color:initial;text-decoration-style:initial;text-decoration-thickness:initial;text-indent:0px;text-transform:none;user-select:text;white-space:normal;widows:2;word-spacing:0px;"&gt;&lt;p class="MsoNormal"&gt;&lt;span style="color:black;"&gt;&lt;i style="mso-bidi-font-style:normal;"&gt;&lt;span style="font-family:&amp;quot;Microsoft Sans Serif&amp;quot;,sans-serif;font-size:11.0pt;layout-grid-mode:line;mso-bidi-font-size:10.0pt;"&gt;On successful completion of the course students should be able to:&amp;nbsp;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/i&gt;&lt;/span&gt;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills)&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;ILO1 – Apply knowledge of f-element coordination/organometallic chemistry to create synthetic routes to complexes with designer geometries, coordination numbers and bonding regimes. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO2 – Interpret a range of experimental data to rationalise physicochemical properties and to propose f-element complex formulations and formal oxidation states at metal and ligand sites. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO3 – Apply knowledge of metal coordination spheres and redox chemistry to generate synthetic routes to f-element complexes with low and high formal metal oxidation states. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO4 – Predict and explain the outcomes of small molecule activation reactions of f-element complexes by consideration of experimental data, ligand effects, covalency and redox chemistry. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO5 – Classify f-element complexes containing redox non-innocent ligands and appraise data to interpret or to hypothesise aspects of structure, bonding and reactivity. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO6 – Compare and contrast lanthanide- and actinide-ligand multiple bonding regimes in order to rationalise relative complex stabilities and their reactivity profiles.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;ILO1 – Interpret reactions commonly used in catalytic asymmetric synthesis.&lt;/p&gt;&lt;p&gt;ILO2 - Predict the outcomes of unseen catalytic asymmetric reactions based on theoretical models.&lt;/p&gt;&lt;p&gt;ILO3 – Develop strategies for the synthesis of unseen molecules using catalytic, asymmetric transformations.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;New topic to be confirmed (J. Abbenseth)&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO1 - &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO2 – &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO3 – &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO4 – &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;ILO1 – describe the effects of heteroatoms on the reactivity of organic molecules containing them.&lt;/p&gt;&lt;p&gt;ILO2 – explain how the presence of a heteroatom modifies the reactivity of an organic compound containing it.&lt;/p&gt;&lt;p&gt;ILO3 – deduce the structure of appropriate heteroatom-containing reagents required to achieve given transformations.&lt;/p&gt;&lt;p&gt;ILO4 – deduce the structure of products formed from organic reactions involving given heteroatom-containing reagents.&lt;/p&gt;&lt;p&gt;ILO5 – write curly-arrow mechanisms for reactions involving heteroatom-containing organic reagents.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal-Organic Frameworks (Y. Ma) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;ILO1 - Revision of metal-ligand coordination chemistry and explore their application in the assembly of extended “infinite” framework structures. Understand the concept of coordination geometry for multiple nuclear metal clusters and analysis of structural connectivity.&lt;/p&gt;&lt;p&gt;ILO2 – Introduction of new advanced characterisation techniques for solid materials. Explore neutron scattering and understand the key </Content>
  </LearningOutcomes>
  <Knowledge Applicant="Y" Label="Knowledge and understanding" Student="Y">
    <Content></Content>
  </Knowledge>
  <IntellectualSkills Applicant="Y" Label="Intellectual skills" Student="Y">
    <Content></Content>
  </IntellectualSkills>
  <PracticalSkills Applicant="Y" Label="Practical skills" Student="Y">
    <Content></Content>
  </PracticalSkills>
  <TransferableSkills Applicant="Y" Label="Transferable skills and personal qualities" Student="Y">
    <Content>&lt;p&gt;Problem solving, analytical skills, time management.&amp;nbsp;&lt;/p&gt;</Content>
  </TransferableSkills>
  <EmployabilitySkillsList Applicant="Y" Label="Employability skills" Student="Y">
    <Skill>
      <SkillId></SkillId>
      <SkillDescription></SkillDescription>
    </Skill>
  </EmployabilitySkillsList>
  <Syllabus Applicant="Y" Label="Syllabus" Student="Y">
    <Content>&lt;div style="border:1.0pt solid windowtext;mso-border-alt:solid windowtext .5pt;mso-element:para-border-div;padding:1.0pt 6.0pt 1.0pt 4.0pt;"&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills)&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;1. Synthetic routes to designer f-element complex geometries and coordination numbers.&lt;/p&gt;&lt;p&gt;2. Experimental determination of oxidation state and covalency in f-element complexes.&lt;/p&gt;&lt;p&gt;3. Achieving the lowest and highest f-element oxidation states.&lt;/p&gt;&lt;p&gt;4. Small molecule activation reactions of f-element complexes.&lt;/p&gt;&lt;p&gt;5. f-Element complexes of redox non-innocent ligands, including arenes.&lt;/p&gt;&lt;p&gt;6. f-Element metal-ligand multiple bonding.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;1) Principles of asymmetric synthesis&lt;/p&gt;&lt;p&gt;2) Catalytic asymmetric 1,2-C=O bond addition&lt;/p&gt;&lt;p&gt;3) Enamine catalysis and HPESW reaction&lt;/p&gt;&lt;p&gt;4) Iminium and chiral acid catalysis&lt;/p&gt;&lt;p&gt;5) TM-catalyzed asymmetric C=C bond hydrogenation&lt;/p&gt;&lt;p&gt;6) Catalytic asymmetric C=O bond reduction&lt;/p&gt;&lt;p&gt;7) Catalytic asymmetric alkene epoxidation&lt;/p&gt;&lt;p&gt;8) Catalytic asymmetric alkene dihydroxylation &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;New topic to be confirmed (J. Abbenseth)&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;This topic will cover...&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;Properties of bonds to silicon; effects of silicon on charges.&lt;/p&gt;&lt;p&gt;Silicon-oxygen bonds: protecting groups, trapping reagents, silyl enol ethers.&lt;/p&gt;&lt;p&gt;Formation and reactions of vinyl silanes&lt;/p&gt;&lt;p&gt;Formation and reactions of allyl silanes&lt;/p&gt;&lt;p&gt;Formation and reactions of anions stabilised by silicon.&lt;/p&gt;&lt;p&gt;Formation and reactions of carbanions stabilised by sulphur: the Julia alkene synthesis.&lt;/p&gt;&lt;p&gt;Dithians, sulfoxides and sulfones.&lt;/p&gt;&lt;p&gt;Formation and reactions of sulfur ylids.&lt;/p&gt;&lt;p&gt;Reactions of allyl sulfoxides: [2,3]-sigmatropic rearrangements.&lt;/p&gt;&lt;p&gt;Reactions of electrophilic sulfur and selenium reagents.&lt;/p&gt;&lt;p&gt;The Pummerer rearrangement.&lt;/p&gt;&lt;p&gt;Phosphorus-containing reagents: the Wittig reaction&lt;/p&gt;&lt;p&gt;Stereoselctivity in the Wittig reaction&lt;/p&gt;&lt;p&gt;Use of phosphonate anions.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal-Organic Frameworks (Y. Ma) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;ol&gt;&lt;li&gt;Introduction to metal-organic frameworks&lt;/li&gt;&lt;li&gt;General synthetic methods of metal-organic frameworks&lt;/li&gt;&lt;li&gt;Characterisation of metal-organic frameworks&lt;/li&gt;&lt;li&gt;Gas adsorption in metal-organic frameworks Chemical Concepts from Quantum&amp;nbsp;&lt;/li&gt;&lt;/ol&gt;&lt;p&gt;&lt;strong&gt;Chemical Concepts from Quantum Mechanics (P. Popelier)&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;The electron density and its Laplacian&lt;/p&gt;&lt;p&gt;The quantum atom and its properties (charge, energy, dipole moment,..)&lt;/p&gt;&lt;p&gt;The mathematical language of dynamical system&lt;/p&gt;&lt;p&gt;Energy partitioning scheme (“Interacting Quantum Atoms”, IQA)&lt;/p&gt;&lt;p&gt;Characterisation of chemical bonding&lt;/p&gt;&lt;p&gt;Electron Distribution Function (EDF)&lt;/p&gt;&lt;p&gt;Electron Localisation Function (ELF)&lt;/p&gt;&lt;p&gt;Electron Localisation-Delocalisation Matrices (LDMs)&amp;nbsp;&lt;span style="color:black;"&gt;&lt;span style="font-family:&amp;quot;Microsoft Sans Serif&amp;quot;,sans-serif;font-size:11.0pt;layout-grid-mode:line;mso-bidi-font-size:10.0pt;"&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;</Content>
  </Syllabus>
  <TeachingMethods Applicant="Y" Label="Teaching and learning methods" Student="Y">
    <Content></Content>
  </TeachingMethods>
  <AssessmentMethods Applicant="Y" Label="Assessment methods" Student="Y">
    <IntroText> </IntroText>
    <Method>
      <MethodId>1</MethodId>
      <MethodName>Written exam</MethodName>
      <MethodWeight>100%</MethodWeight>
    </Method>
  </AssessmentMethods>
  <FeedbackMethods Applicant="Y" Label="Feedback methods" Student="Y">
    <Content>&lt;div&gt;&lt;div style="border:1.0pt solid windowtext;mso-border-alt:solid windowtext .5pt;mso-element:para-border-div;padding:1.0pt 6.0pt 1.0pt 4.0pt;"&gt;&lt;p&gt;Lecturing staff will provide office hours during the course&lt;/p&gt;&lt;p&gt;After the exam marking has been completed, students are provided with feedback&amp;nbsp;&lt;span style="color:black;"&gt;&lt;span style="font-family:&amp;quot;Microsoft Sans Serif&amp;quot;,sans-serif;font-size:11.0pt;layout-grid-mode:line;mso-bidi-font-size:10.0pt;"&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;</Content>
  </FeedbackMethods>
  <RequirementsList Applicant="Y" Label="Pre/co-requisites" Student="Y">
    <Requirement>
      <UnitCode></UnitCode>
      <UnitTitle></UnitTitle>
      <RequirementType></RequirementType>
      <Description></Description>
    </Requirement>
    <AdditionalRequirement>&lt;p&gt;Pre-requisite units: Core chemistry&amp;nbsp;&lt;/p&gt;</AdditionalRequirement>
  </RequirementsList>
  <AcademicPrograms Applicant="Y" Label="Academic programmes" Student="Y">
    <AcademicProgram>
      <Program></Program>
      <Plan></Plan>
      <Level></Level>
      <Requirement></Requirement>
    </AcademicProgram>
  </AcademicPrograms>
  <FreeChoice Applicant="Y" Label="Available as a free choice unit?" Student="Y">
    <Content>N</Content>
  </FreeChoice>
  <Accreditation Applicant="Y" Label="Accreditation" Student="Y">
    <Content></Content>
  </Accreditation>
  <RecommendedReading Applicant="Y" Label="Recommended reading" Student="Y">
    <Content>&lt;div&gt;&lt;div&gt;&lt;div style="border:1.0pt solid windowtext;mso-border-alt:solid windowtext .5pt;mso-element:para-border-div;padding:1.0pt 6.0pt 1.0pt 4.0pt;"&gt;&lt;p class="MsoNormal" style="border-style:none;mso-border-alt:solid windowtext .5pt;mso-padding-alt:1.0pt 6.0pt 1.0pt 4.0pt;padding:0cm;"&gt;&lt;span style="color:black;"&gt;&lt;span style="font-family:&amp;quot;Microsoft Sans Serif&amp;quot;,sans-serif;font-size:11.0pt;layout-grid-mode:line;mso-bidi-font-size:10.0pt;"&gt;Specific reading material will be provided separately for each topic.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;</Content>
  </RecommendedReading>
  <StudyHours Applicant="Y" Label="Study hours" Student="Y">
    <IntroText> </IntroText>
    <ScheduledHours Applicant="Y" Label="Scheduled activity hours" Student="Y">
      <ActivityHours>
        <ActivityType>Assessment written exam</ActivityType>
        <Hours>2</Hours>
      </ActivityHours>
      <ActivityHours>
        <ActivityType>eAssessment</ActivityType>
        <Hours>5</Hours>
      </ActivityHours>
      <ActivityHours>
        <ActivityType>Lectures</ActivityType>
        <Hours>8</Hours>
      </ActivityHours>
      <ActivityHours>
        <ActivityType>Supervised time in studio/wksp</ActivityType>
        <Hours>8</Hours>
      </ActivityHours>
      <ActivityHours>
        <ActivityType>Work based learning</ActivityType>
        <Hours>12</Hours>
      </ActivityHours>
    </ScheduledHours>
    <PlacementHours Applicant="Y" Label="Placement hours" Student="Y">
      <ActivityHours>
        <ActivityType></ActivityType>
        <Hours>0</Hours>
      </ActivityHours>
    </PlacementHours>
    <TotalHours Applicant="Y" Label="Independent study hours" Student="Y">
      <Hours>65</Hours>
    </TotalHours>
  </StudyHours>
  <Notes Applicant="Y" Label="Additional notes" Student="Y">
    <Content></Content>
  </Notes>
</CourseUnit>
