Victorian Certificate of Education 2012 CHEMISTRY Written examination Day Date 2012 Reading time: *.** to *.** (15 minutes) Writing time: *.** to *.** (1 hour 30 minutes) DATA BOOK Directions to students • A question and answer book is provided with this data book. Students are NOT permitted to bring mobile phones and/or any other unauthorised electronic devices into the examination room. © VICTORIAN CURRICULUM AND ASSESSMENT AUTHORITY 2012 2012 CHEM DATA BOOK 2 Table
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Lab 5 n-Butyl Bromide Preparation Introduction: The purpose of this lab is to properly extract and distill n-butyl bromide It is ideal to perform this technique with accuracy‚ which can be measured by the percent yield. Chemicals: n-Butyl Bromide- clear‚ yellow liquid that is slightly soluble in water. Molar weight of 137.02g and has zero reactivity. Sodium Bromide- white‚ crystals‚ granules. Soluble in water with no reactivity. Molar weight of 102.89g. Sulfuric Acid- colorless liquid
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t-Pentyl Chloride is a compound that is created through an SN1 nucleophilic substitution reaction in addition with Hydrogen Chloride in order to isolate the product. A variety of procedural techniques were utilized during the experiment including extraction‚ washing liquids‚ drying liquids‚ gravity filtration‚ and simple distillation. When a single solute or compound is transferred between two different solutes‚ it is known as extraction. Another technique that was utilized was washing‚ in which
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Procedure The procedure stated in Chem 2120 experiment 6 Williamson Ether Synthesis of Phenacetin laboratory manual was followed without any major changes. Data and results Compound Amount used MW (g/mol) Moles Stoichiometry/Comments acetaminophen 0.354 g 151.16 2.34 x 10-3 limiting reagent ethyl iodide 0.3mL 155.97 3.75 x 10-3 1.6 equiv ’s sodium ethoxide 2.6mL 68.05 3.3 x 10-2 catalyst‚ reaction solvent crude product obtained: phenacetin 0.32g
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CHEM 2123 and 2125 – Organic Chemistry Lab I and II GUIDELINES FOR WRITING LAB REPORTS INTRODUCTION Writing reports in organic chemistry lab may differ from the way it’s done in general chemistry. One goal of this course is to introduce you to the record keeping methods used in research labs. Such methods are designed to organize experimental data in a format similar to that required for publication in major scientific journals. Here are some important considerations that apply in research settings
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Topic Acid-Base Theory (Unit 1) Acid-Base Theory (Unit 2) Isomerism (Unit 1) Isomerism (Unit 2) Nomenclature Reaction Mechanism (Unit 1) - Introduction to Mechanism Reaction Mechanism (Unit 2) - Nucleophilic substitution Reaction Mechanism (Unit 3) - Nucleophilic substitution Reaction Mechanism (Unit 4) - Nucleophilic substitution Reaction Mechanism (Unit 5) - Nucleophilic substitution Reaction Mechanism (Unit 6) - Nucleophilic substitution Reaction Mechanism (Unit 7) - Elimination Reaction Mechanism
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Introduction The purpose of this lab is to synthesize Lidocaine from 2‚6-dimethylaniline‚ using diethyl amine‚ 2-chloroacetyl chloride‚ acetic acid‚ and toluene. The Lidocaine was made by adding 2‚6-dimethylaniline to 2-chloroacetyl chloride in acetic acid. Sodium acetate is added in order to make the compound soluble. The product is dried‚ then treated with diethyl amine and toluene. This is refluxed using a water-cooled reflux condenser. The vapor is condensed by the cold water as the compound
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William B. Heard Rigid Body Mechanics William B. Heard Rigid Body Mechanics Mathematics‚ Physics and Applications WILEY-VCH Verlag GmbH & Co. KGaA The Author William B. Heard Alexandria‚ VA USA For a Solutions Manual‚ lecturers should contact the editorial department at physics@wiley-vch.de‚ stating their affiliation and the course in which they wish to use the book All books published by Wiley-VCH are carefully produced. Nevertheless‚ authors‚ editors‚ and publisher do not warrant the information
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TSINGHUA SCIENCE AND TECHNOLOGY ISSN ll 1007-0214 ll10/10 llpp599-605 Volume 17‚ Number 5‚ October 2012 CoP: An Ultra-Lightweight Secure Network Coding Scheme via Last Forwarder’s Proof Wei Ren1;2; ‚ Linchen Yu1 ‚ Liangli Ma3 1. School of Computer Science‚ China University of Geosciences‚ Wuhan 430074‚ China; 2. Shandong Provincial Key Laboratory of Computer Network‚ Jinan 250014‚ China; 3. Department of Computer Engineering‚ Naval University of Engineering‚ Wuhan 430033‚ China Abstract: Network
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