School of Chemistry | Faculty of Science | The University of Sydney
Periodic Table (PDF) | Useful Data | Useful Formulas | Link to RSS feed | Link to Twitter site | Link to Facebook page | Bookmark and Share

CHEM1102 - Syllabus


Chemistry 1B


Week

Topics covered

1
Representations of Molecular Structure
- revise VSEPR, bonding and shape
- shape and hybridisation for alkanes, alkenes and alkynes
- stick notation
- functional groups and nomenclature

Alkanes
- constitutional isomers
- conformational isomers
- cis/trans isomers of cyclic alkanes

Alkenes
- pi-bonds and structure
- E/Z isomers
- introduction to organic mechanisms
- addition reactions, mechanism of electrophilic addition
- Markovnikov's rule: carbocation stability
- reaction summary (addition reactions, orientation of addition and carbocation stability)

Alkynes
- addition reactions

Aromatic Compounds
- benzene: aromaticity, resonance
- electrophilic aromatic substitution (bromination only)
- compare to alkenes
2

Structural Determination
- mass spectrometry
- infrared spectroscopy
- UV-visible spectroscopy
- 1H NMR spectroscopy
- MRI and medical applications
- problem solving exercises

Alcohols
- structure of alcohols, phenols and ethers
- H-bonding and physical properties of alcohols
- acid-base reactions of alcohols & phenols: resonance stabilisation and stability of conjugate base
-oxidation reactions
-elimination reactions and Zaitsev's rule

Amines
- structure of amines
- H-bonding and physical properties of amines
- amines as bases

Stereochemistry
- stereogenic centres
- optical activity
- (R), (S) nomenclature
- racemic mixtures
- importance of chirality in nature and drug design
3
Organic Halogen Compounds
- substitiution reactions and scope
- SN1 and SN2 mechanisms: compare carbocation stability and steric hindrance
- consequences of stereochemistry
- elimination reactions
- Grignard formation

Aldehydes and Ketones
- structure and polatiry
- nucleophilic addition reactions of Grignard reagents and hydride reducing agents
- oxidation of aldehydes

Carboxylic Acids and Derivatives
- carboxylic acids
- acidity and resonance stabilisation of conjugate base
- reduction to primary alcohols
- formation of acid chlorides
- derivatives (acid halides, anhydrides, esters and amides)
- acid halides, anhydrides, esters & amides
- relative reactivity of carboxylic acid derivatives
- interconversion and hydrolysis of derivatives
- polymers and example of nylon66

Synthetic Strategies
- design of target molecules
- problem solving
4
Strong Acids and Bases
- electrolytes - strong and weak
- autoionisation of water
- conjugate acid-base pairs

Weak Acids and Bases
- carboxylic acids, carbonic acids, phenols
- ammonia, amines
5
Calculations Involving pKa
- calculations involving pKa and pKb
- buffers
- common ion effect

Periodic Trends in Aqueous Oxides
- acids and bases

Physical States and Phase Diagrams
- single component
- enthalpy change
- entropy (qualitative) in gas-liquid equilibrium and endothermicity
- trends in elemental freezing and boiling points

Intermolecular Forces and Phase Behaviour
- boiling point trends
- solid structure (ice, etc.)
- water/salt equilibrium, saturated solutions
- alloys
- miscibility

Crystal Structures

Solubility Equilibrium
- calculations involving Ksp
- solubility trends as a function of polarity of solvents (e.g. alcohols in water)
- solubility of ionic solids
- role of intermolecular forces in solubility
- heats of solvation
6
Hydrolysis of Metal Ions
- introduction to the ligand bond

Metals in Biology
- introduction to transition metals

Coordination Chemistry
- complexes
- cis/trans
- oxidation states
- colour

Kinetics
- variability of reaction rates
- review of 1st order rate constants from nuclear chemistry and introduction to 2nd order rate constants
- mechanism and rate determining steps

Kinetics - Influences
- temperature and the Arrhenius relation
- diffusion constants
- solvent polarity

Kinetics - Catalysis
- altering the mechanism
- industrial example
- enzymes
 



Textbook


Blackman, Bottle, Schmid, Mocerino and Wille,
     Chemistry, 3rd Edition, 2015 (John Wiley) ISBN: 978-0-7303-1105-8 (paperback) and 978-0-7303-2492-8 (e-text)


Textbook resources, including the answers to the odd-numbered problems of Chemistry, 3rd Edition and the web address for the publisher's site, are available via "Textbook Resources" on USYD eLearning.


Contact Us | Privacy | ©2017 School of Chemistry | last modified Friday, 21 February, 2014 :: top of the page ::