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    To solve a system of equations by addition or subtraction (or elimination)‚ you must eliminate one of the variables so that you could solve for one of the variables. First‚ in this equation‚ you must look for a way to eliminate a variable (line the equations up vertically and look to see if there are any numbers that are equal to each other). If there is lets say a –2y on the top equation and a –2y on the bottom equation you could subtract them and they would eliminate themselves by equaling zero

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    Synthesis of an Alkyl Halide

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    Preparations of alkyl halides. Retrieved from http://www.mhhe.com/physsci/chemistry/carey/student/olc/ch04prepare.html (5) McMurry‚ J.E. Organic chemistry‚ 7th ed.; Thompson Learning‚ Inc.: California‚ 2008‚ pp. 215-218; 335-339; 344-345 (6) Norris‚ P. Elimination reactions. Retrieved from http://www.hyperconjugation.com/teaching/3719files/mechanisms/elimination.html (7) Institute of Chemisty‚ University of the Philippines. Organic chemistry laboratory manual‚ 2008 ed.; University of the Philippines: Manila

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    Formal Report

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    order of: μ= C-Cl > 1.56D C-F > 1.51D C-Br > 1.48D C-I 1.29D Ch06 Alkyl Halides Page 1 Typically the chemistry of alkyl halides is dominated by this effect‚ and usually results in the C-X bond being broken (either in a substitution or elimination process). This reactivity makes alkyl halides useful chemical reagents. Nomenclature According to IUPAC‚ alkyl halides are treated as alkanes with a halogen substituent. The halogen prefixes are Fluoro-‚ Chloro-‚ Bromo- and Iodo-. Examples: H Cl

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    y BACHELOR OF COMPUTER APPLICATIONS (BCA) ASSIGNMENTS Year‚ 2013-2014 (5th Semester (Revised Syllabus)) (BCS-051‚ BCS-052‚ BCS-053‚ BCS-054‚ BCS-055‚ BCSL-056‚ BCSL-057‚ BCSL-058) SCHOOL OF COMPUTER AND INFORMATION SCIENCES INDIRA GANDHI NATIONAL OPEN UNIVERSITY MAIDAN GARHI‚ NEW DELHI – 110 068 CONTENTS Course Code Assignment No. Submission-Schedule Page No. For July-Dec 2013 Session For Jan-June 2014 Session BCS-051 BCA(V)-051/Assign/13-14 15th October

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    Alkenes by Elimination Kyle Peterson Chem. 243a Matt Judd‚ Sec. 25 Date Performed: 11/12/03 Abstract: The objective of this experiment is to successfully perform a dehydration of a 2-butanol and a dehydrohalogenation of 2-bromobutane to form the products 1-butene‚ trans-2-butene‚ and cis-2-butene. It was found that a dehydration of 2-butanol yielded 4.6% 1-butene‚ 67.3% trans-2-butene‚ and 28.1% cis-2-butene‚ and a dehydrohalogenation of 2-bromobutane yielded 19.1% 1-butene‚ 69.9% trans-2-butene

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    Alcohol and Ir Spectrum

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    Conversion of Alcohols to Alkyl Halides Title: Conversion of Alcohols to Alkyl Halides Abstract: In this experiment the conversion of alcohols to alkyl halides are investigated through reflux and simple distillation. These are common procedures used to separate substances. After the reflux and distillation is complete 13C NMR and IR spectrum is used to identify the product or products for each reaction: 1a‚ 1b‚ and 2. Every individual in the group was assigned either 1a (1-propanol) or 1b (2-pentanol)

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    General Assembly: 2 Human Rights Topic: Elimination of ethnic and religious discrimination Country: Tunisia Delegate: John Marco The word discrimination can be defined as‚ “treatment or consideration of‚ or making a distinction in favor of or against‚ a person or thing based on the group‚ class‚ or category to which that person or thing belongs rather than on individual merit.” One large type of discrimination in the world of today is religious and ethnic discrimination. Religious and ethnic

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    Experiment #7 Fall 2014 Dehydration of an alcohol NAME Nick Weinberger POSTLAB 1. Show the mechanism for the dehydration of -tetralol under conditions employed in the lab. Show all intermediates‚ and show electron flow with arrows. 2. What general mechanism most likely applies to this reaction (SN2‚ E2 etc)? E1 3. Why was acid employed in this reaction? The acid was used to protonate the leaving group (OH) to form water which is a much better leaving

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    Competing Nucleophiles Lab

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    Title: Competing Nucleophiles (Exp 24‚ pp 211-221‚ pp 808-823‚ pp 836-842) Purpose: The purpose of this experiment is to determine the nucleophilic strength of chloride and bromide ions as it reacts with 1-butanol (n-butyl) and 2-methyl-2-propanol (t-butyl alcohol) under SN1 and SN2 conditions. Method: 40 g of ice and approximately 30 ml of sulfuric acid is cautiously added to a 100 mL beaker respectively. Weigh 7.6 g of ammonium chloride and 14.0 g of ammonium bromide and place it in

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    Gauss-Jordan Matrix Elimination -This method can be used to solve systems of linear equations involving two or more variables. However‚ the system must be changed to an augmented matrix. -This method can also be used to find the inverse of a 2x2 matrix or larger matrices‚ 3x3‚ 4x4 etc. Note: The matrix must be a square matrix in order to find its inverse. An Augmented Matrix is used to solve a system of linear equations. a1 x + b1 y + c1 z = d1 a 2 x + b2 y + c 2 z = d 2 a3 x + b3 y + c3 z = d 3

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