Friday, August 18, 2017

Unit 4 - Area of Study 2 - What is the chemistry of food

Unit 4: How are organic compounds categorised, analysed and used?


TIPS AND TRICKS TO BOOST YOUR YEAR 12 SCORES - Unimelb


Area of Study 2 - What is the chemistry of food?

Food contains various organic compounds that are the source of both the energy and the raw materials that the human body needs for growth and repair. In this area of study students explore the importance of food from a chemical perspective. Students study the major components of food with reference to their structures, properties and functions. They examine the hydrolysis reactions in which foods are broken down, the condensation reactions in which new biomolecules are formed and the role of enzymes, assisted by coenzymes, in the metabolism of food. Students study the role of glucose in cellular respiration and investigate the principles of calorimetry and its application in determining enthalpy changes for reactions in solution. They explore applications of food chemistry by considering the differences in structures of natural and artificial sweeteners, the chemical significance of the glycaemic index of foods, the rancidity of fats and oils, and the use of the term ‘essential’ to describe some amino acids and fatty acids in the diet. (VCAA study design)

Key food molecules

• proteins: formation of dipeptides and polypeptides as condensation polymers of 2-amino acids; primary (including peptide links), secondary, tertiary and quaternary structure and bonding; distinction between essential and non-essential amino acids as dietary components

• carbohydrates: formation of disaccharides from monosaccharides, and of complex carbohydrates (specifically starch and cellulose) as condensation polymers of monosaccharides; glycosidic links; storage of excess glucose in the body as glycogen; comparison of glucose, fructose, sucrose and the artificial sweetener aspartame with reference to their structures and energy content

• fats and oils (triglycerides): common structural features including ester links; distinction between fats and oils with reference to melting points; explanation of different melting points of triglycerides with reference to the structures of their fatty acid tails and the strength of intermolecular forces; chemical structures of saturated and unsaturated (monounsaturated and polyunsaturated) fatty acids; distinction between essential and nonessential fatty acids; and structural differences between omega-3 fatty acids and omega-6 fatty acids

• vitamins: inability of humans to synthesise most vitamins (except Vitamin D) making them essential dietary requirements; comparison of structural features of Vitamin C (illustrative of a water-soluble vitamin) and Vitamin D (illustrative of a fat-soluble vitamin) that determine their solubility in water or oil.

Metabolism of food in the human body

• metabolism of food as a source of energy and raw materials: general principles of metabolism of food involving enzyme-catalysed chemical reactions with reference to the breakdown of large biomolecules in food by hydrolytic reactions to produce smaller molecules, and the subsequent synthesis of large biologically important molecules by condensation reactions of smaller molecules

• enzymes as protein catalysts: active site; modelling of process by which enzymes control specific biochemical reactions (lock-and-key and induced fit models); consequences of variation in enzyme-substrate interaction (lock-and-key mechanism) due to the behaviour of a particular optical isomer; explanation of effects of changes in pH (formation of zwitterions and denaturation), increased temperature (denaturation) and decreased temperature (reduction in activity) on enzyme activity with reference to structure and bonding; action of enzymes in narrow pH ranges; and use of reaction rates to measure enzyme activity

• the distinction between denaturation of a protein and hydrolysis of its primary structure

• hydrolysis of starch in the body: explanation of the ability of all humans to hydrolyse starch but not cellulose, and of differential ability in humans to hydrolyse lactose; glycaemic index (GI) of foods as a ranking of carbohydrates based on the hydrolysis of starches (varying proportions of amylose and amylopectin) to produce glucose in the body

• hydrolysis of fats and oils from foods to produce glycerol and fatty acids; oxidative rancidity with reference to chemical reactions and processes, and the role of antioxidants in slowing rate of oxidative rancidity

• the principles of the action of coenzymes (often derived from vitamins) as organic molecules that bind to the active site of an enzyme during catalysis, thereby changing the surface shape and hence the binding properties of the active site to enable function as intermediate carriers of electrons and/or groups of atoms (no specific cases required).

Energy content of food

• the comparison of energy values of carbohydrates, proteins and fats and oils

• glucose as the primary energy source, including a balanced thermochemical equation for cellular respiration

• the principles of calorimetry; solution and bomb calorimetry, including determination of calibration factor and consideration of the effects of heat loss; and analysis of temperature-time graphs obtained from solution calorimetry.

Videos

Induced Fit Model of Enzymes

Lock and Key vs Induced Fit Model of Enzymes
Protein Hydrolysis

Oxidation Rancidity

Saturated, Mono & Poly Unsaturated Fats

Denaturation of Proteins

Condensation Reation

Zwitterions - non-charged amino acids with opposite charges either end

Titration calculation of Vitamin C

Oxidation and Reduction (OIL-RIG)

Carbon atom - Introduction

Water

carbohydrates, lipids, and proteins

Cellular respiration

Photosynthesis
Making Proteins
Proteins - Nutrition, vitamins

Polymers

Resources:

VCAA

Chemistry Study Design
Chemistry Past Exams VCAA
Chemistry Data book 2017 - NEW
VCAA Assessment Rubric - Unit 4 Area of Study 1

Class Resources

Resources from Chemistry Professsional Development

Pat O'Shea's Chemistry webpage

Sunday, June 11, 2017

Unit 4 - Area of Study 1 - How are organic compounds categorised, analysed and used?

Unit 4: How are organic compounds categorised, analysed and used?


Area of Study 1 - How can the diversity of carbon compounds be explained and categorised? 


Structure and nomenclature of organic compounds 


-the carbon atom with reference to valence number, bond strength, stability of carbon bonds with other elements and the formation of isomers (structural and stereoisomers) to explain carbon compound diversity, including identification of chiral centres in optical isomers of simple organic compounds and distinction between cis- and trans- isomers in simple geometric isomers

-structures including molecular, structural and semi-structural formulas of alkanes (including cyclohexane), alkenes, alkynes, benzene, haloalkanes, primary amines, primary amides, alcohols (primary, secondary, tertiary), aldehydes, ketones, carboxylic acids and non-branched esters

-IUPAC systematic naming of organic compounds up to C8 with no more than two functional groups for a molecule, limited to non-cyclic hydrocarbons, haloalkanes, primary amines, alcohols (primary, secondary, tertiary), carboxylic acids and non-branched esters.


(From VCAA chemistry study design)


Prefix = added in front of word ( E.g. re-turn )

Suffix = added at end of word (E.g. Alk-anes )

Kind of bond (Added as suffix)

Alkanes - 1 bond (single bond) - Saturated 
Alkenes = 2 bond (double bond) - Unsaturated (1 or more double bond)
Alkynes  3 bond (triple bond)

Geometric orientation (Added as prefix)

cis- means on the same side
trans- means across

Number of carbon atoms (Added as prefix)

meth - 1 carbon
eth    - 2 carbon
prop - 3 carbon
but    - 4 carbon
pent - 5 carbon
hex   - 6 carbon
hept - 7 carbon
oct   - 8 carbon


Alkanes - single bonded hydrocarbons
Alkenes = double bonded, Alkyne  3 bonded
Aromatics and Cyclic Compounds
Functional groups
Alcohols, Hydroxyl Groups, Aldehydes, Carboxylic Acid. Acetone is a Ketone, Ethers and Esters, Amines
Nomenclature - IUPAC systematic naming of organic compounds




Categories, properties and reactions of organic compounds

• an explanation of trends in physical properties (boiling point, viscosity) and flashpoint with reference to structure and bonding

 • organic reactions, including appropriate equations and reagents, for the oxidation of primary and secondary alcohols, substitution reactions of haloalkanes, addition reactions of alkenes, hydrolysis reactions of esters, the condensation reaction between an amine and a carboxylic acid, and the esterification reaction between an alcohol and a carboxylic acid 

• the pathways used to synthesise primary haloalkanes, primary alcohols, primary amines, carboxylic acids and esters, including calculations of atom economy and percentage yield of single-step or overall pathway reactions.

(From VCAA chemistry study design)

Analysis of organic compounds

• the principles and applications of mass spectroscopy (excluding features of instrumentation and operation) and interpretation of qualitative and quantitative data, including identification of molecular ion peak, determination of molecular mass and identification of simple fragments 

• the principles and applications of infrared spectroscopy (IR) (excluding features of instrumentation and operation) and interpretation of qualitative and quantitative data including use of characteristic absorption bands to identify bonds 

• the principles (including spin energy levels) and applications of proton and carbon-13 nuclear magnetic resonance spectroscopy (NMR) (excluding features of instrumentation and operation); analysis of carbon-13 NMR spectra and use of chemical shifts to determine number and nature of different carbon environments in a simple organic compound; and analysis of high resolution proton NMR spectra to determine the structure of a simple organic compound using chemical shifts, areas under peak and peak splitting patterns (excluding coupling constants) and application of the n+1 rule 

• determination of the structures of simple organic compounds using a combination of mass spectrometry (MS), infrared spectroscopy (IR) and proton and carbon-13 nuclear magnetic resonance spectroscopy (NMR) (limited to data analysis) 

• the principles of chromatography including use of high performance liquid chromatography (HPLC) and construction and use of a calibration curve to determine the concentration of an organic compound in a solution 

• determination of the concentration of an organic compound by volumetric analysis, including the principles of direct acid-base and redox titrations (excluding back titrations).

(From VCAA chemistry study design)

Spectroscopy



Mass spectrometry




Infrared (IR) spectrometry
Nuclear magnetic resonance (NMR) spectrometry
High performance liquid chromatography (HPLC)
Volumetric analysis - titration


Resources:

VCAA

Chemistry Study Design
Chemistry Past Exams VCAA
Chemistry Data book 2017 - NEW
VCAA Assessment Rubric - Unit 4 Area of Study 1

Class Resources

Resources from Chemistry Professsional Development

Pat O'Shea's Chemistry webpage

Thursday, April 20, 2017

Unit 3 - Area of Study 2 - How can the yield of a chemical product be optimised?

Rates of chemical reactions

-Collision Theory
-Maxwell-Boltzman distributions
-Energy profiles (Endo&Exo)
-Factors affecting rate of reactions
-Catalysts

1. Presentation - Rates of reactions
2. Presentation - Ch7&8 with test/quiz


Extent of chemical reactions - Equilibrium

-Reversible and irreversible reactions
-Homogeneous equilibria
-Equilibrium constant "Kc"
-Le Chatelier's Principle
-Percentage yield





Production of chemicals by electrolysis












Rechargeable batteries


Study Tips - Feynman technique



Friday, February 3, 2017

Unit 3 - Area of study 1 

What are the options for energy production?

Online Quizzes

Chapter 1 - Fuels       Password: 000 (triple zero)

Events:

Experiments

Experiment 1 - Fractional Distillation of Crude Oil


Topics

Fuel choices

Comparison of fossil fuels and Biofuels

Fossil Fuels - coal, crude oil, petroleum gas, coal seam gas.
Fossil fuels are non-renewable fuels that are mined for underground.


Biofuels - biogas, bioethanol and biodiesel

Biofuels are a fuel derived immediately from living matter (Plants, animal waste, ect)


Comparison of the suitability of petrodiesel and biodiesel

Petrodiesel is a non-renewable fossil fuel where as biodiesel is a renewable fuel created from plant and animal matter.


Viscosity

Viscosity is a measure of how easy it is for a fluid to flow due to internal friction. I.e. Honey has a high viscosity.


Obtaining energy from fuels

Combustion of fuels

Combustion of fuels is an exothermic reaction (releases heat) where energy is transformed from stored chemical energy in heat, light and sound energy. 


Enthalpy change (ΔH)

The enthalpy change (ΔH) is the amount of heat released or absorbed when a chemical reaction occurs at constant pressure. ΔH = H(products) - H(reactants) ΔH is specified per mole of substance as in the balanced chemical equation for the reaction.




Writing of balanced thermochemical equations



The Universal Gas Equation (PV=nRT) and Standard Laboratory Conditions (SLC)

PV = nRT       SLC = 25 °C and 100 kPa          STP = 0 °C and 100 kPa      0K = -273.15 °C


Stoichiometry

Stoichiometry is the relationship between the relative quantities of substances taking part in a reaction or forming a compound, typically a ratio of whole integers.
Stoichiometry Calculator



Specific heat capacity

Specific heat capacity is the heat required to raise the temperature of the unit mass of a given substance by a given amount (usually one degree).


Galvanic cells as a source of energy

Redox reactions

Redox reactions are An oxidation-reduction (redoxreaction is a type of chemical reaction that involves a transfer of electrons between two species. An oxidation-reductionreaction is any chemical reaction in which the oxidation number of a molecule, atom, or ion changes by gaining or losing an electron.

Writing of balanced half-equations

Galvanic cells

Battery - A galvanic cell, or voltaic cell, named after Luigi Galvani, or Alessandro Volta respectively, is an electrochemical cell that derives electrical energy from spontaneous redox reactions taking place within the cell.


Fuel cells as a source of energy

Fuel cells


Electrolysis - Water to Hydrogen and Oxygen


Compare Fuel cells to combustion fuels and galvanic cells


Yr12 Chemistry 2017

Videos: