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    Ausmat Answers Chemistry 2010

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    Chemistry Stage 3 Standards Guide Exemplification of Standards through the 2010 WACE Examination Chemistry: Stage 3 Standards Guide 1 2010/33606 Copyright © Curriculum Council‚ 2011 This document—apart from any third party copyright material contained in it—may be freely copied‚ or communicated on an intranet‚ for noncommercial purposes by educational institutions‚ provided that it is not changed in any way and that the Curriculum Council is acknowledged as the copyright owner. Copying

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    Polymer Chains

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    Name: Jeff Chudakoff Partners: Alejandra Garcia Date: 2 December 2011 TA: Mengbin Chen Skill Building Exercise #2 Answer the following questions: 1. What does it mean when a polymer is crosslinked? Crosslinked is one manner in which monomers link together. In this method‚ separate polymer chains are connected via bonds between the individual polymer chains. 2. We discussed how polymer linking and structure contribute to its properties. How would you expect the density‚ elasticity

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    Synthesis of Acetanilide Reaction O NH2 + H3C C O O C CH3 O N C CH3 H + H3C O C OH Aniline Acetic anhydride Acetanilide Acetic acid Purpose: Acetanilide is a useful precursor to many pharmaceuticals such as acetaminophen and penicillin. Experimental Procedure. (Estimated time: 1.5 h.) Unless otherwise noted‚ all manipulations should be done in the chemical fume hood. Place 100 µL of aniline into a tared 10 X 75-mm test tube (standing in a small beaker or Erlenmeyer flask). Now add

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    Polymers

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    -NCO‚ etc.‚ Examples: CH3CH2OH one reactive - OH group is present so functionality is one (i.e.‚ monofunctional) CH3COOH monofunctional CH3 (CH2)4 (CH2) NH2 monofunctional HO CH2 CH2 OH two – OH groups are present‚ so bifunctional CH2 (COOH)2 bifunctional H2N CH2 (CH2)4 (CH2) NH2 bifunctional HOOC CH2 CH (COOH) CH2 COOH trifunctional Some compounds‚ however‚ do not contain any reactive functional groups‚ but the presence of double or triple bonds in the molecule

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    Contents 1. Introduction and literature review 1.1 Polypropylene 1.1.1 Polypropylene crystallization 1.2 Polymer degradation 1.3 Broadband dielectric 1.4 Solubility and the cohesive energy density 1.5 Literature review 2. Experimental method 2.1 Solubility of SN 1010 in various solvents 2.2 Calibration curve 2.3 Preparation of polymer/antioxidant mix for films 2.4 Soxhlet extraction 2.5 Broadband dielectric analysis of films 2.6 Broadband dielectric analysis of molten samples

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    55 chem 3341-111 The Preparation of Aspirin The purpose of this experiment is to synthesize aspirin (acetyl salicylic acid) from salicylic acid and acetic anhydride. CO2H OH salicylic acid 2g 0.014 mole O O O CH3 H2SO4 ethyl acetate CO2H O O acetyl salicylic acid acetic acid CH3 O + H3C + H3C OH acetic anhydride 5 mL 0.05 mole The limiting reagent is salicylic acid. The theoretical yield of acetyl salicylic acid is 2.52 g. Physical Data:* mp MW salicylic acid 157-9˚

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    Intermolecular Forces

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    Oakland Schools Chemistry Resource Unit Intermolecular Forces  Brook R. Kirouac  David A. Consiglio‚ Jr.  Southfield‐Lathrup High School Southfield Public Schools    Bonding: Intermolecular Forces Content Statements: C2.2: Chemical Potential Energy Potential energy is stored whenever work must be done to change the distance between two objects. The attraction between the two objects may be gravitational‚ electrostatic‚ magnetic‚ or strong force. Chemical potential energy is the result

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    Mip Tensile Strength

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    (HDPE)‚ General Purpose polystyrene (GPPS) and Polypropylene (PP) in descending order. The reason why HIPS has a higher impact strength than HDPE is because HIPS is made of a larger monomer‚ styrene (C8H8 or C6H5CH=CH2) while HDPE is made of a smaller monomer‚ ethylene (C2H4 or H2C=CH2). Additionally‚ HDPE is a linear polymer. HDPE is made of closely packed structure of ethylene hydrocarbon (C2H4n.H2) which undergoes a catalytic process. There are no branching in the molecular structure‚ resulting

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    Non Premixed Flames

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    AE 6766 Project 3 Nonpremixed Flames Introduction: In order to understand the structure of non-premixed flames‚ this projects employs a type of opposed flow diffusion to generate a nearly one-dimensional an axisymmetric diffusion flame. The one dimensional character of this flame is significant because it reduces complexities compared to a 2 dimensional flame‚ which allows for manageable and practical calculations. Moreover‚ this type of flame can be generated and easily investigated in the

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    DRIED MALUNGGAY (Moringa oleifera) LEAVES IN ETHANOL PRODUCTION A Research Proposal Presented to Carmona National High School Special Science Curriculum In Partial Fulfillment of the Requirements for Research I Proponents: Catangay‚ Jhantal A. Gicana‚ Emchie Elaine R. Marasigan‚ Jan Ian B. Natividad‚ Abigail Jacinthe B. Viaje‚ Kyrinne Kate M. Zara‚ Hazel Jane Muriel C. March 2012 CHAPTER 1 THE PROBLEM AND ITS BACKGROUND We all know that ethanol or ethyl alcohol has a very

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