indicates that there was no side reactions‚ as none of the side product was retrieved. Liquid distill at about 82.8°C‚ which indicates that 2-chloro-2-methylbutane was the only product of this reaction. The theoretical yield was calculated using 2-methyl-2-butanol as the limited reagent in the reaction‚ and was found to be 7.80 grams of 2-chloro-2-methylbutane. The experimental yield that was retrieved was found to be much less‚ at 1.84 grams. The percent yield was calculated to be 23.60% utilizing
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Chem 3411 Dr. Eidell October 24‚ 2014 Preparation and IR Analysis of 2-chloride-2-methylbutane Line Reaction Abstract The purpose of this experiment was to react 2-methyl-2-butanol with concentrated HCl in order to form 2-chloride-2-methylbutane. The hydrogen for the HCl make the -OH from the 2-methyl-2-butanol into a good leaving group because H2O is formed. The H2O leaves and Cl- is free to bond with the carbocation creating 2-chloride-2-methylbutane. The materials needed for the lab were
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Introduction 3 Results 4 Discussion 6 Conclusion 7 Experimental 7 References 8 Preparation of 2-Acetylcyclohexanone Introduction When hydrogens are present on the α-carbon of ketones (like the reaction used in this experiment)‚ carbonyl compounds and aldehydes‚ they turn the compound slightly acidic1. These functional groups are removed by using a basic solution as shown in (i) below1. The product formed with water is stable only due to resonance‚ but does
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Nor Amirah Farhana Nawawi‚ Mia Organic Chemistry Lab Report 2 Jessica Sammons TITLE: Preparation of 2-butanone INTRODUCTION: The goal of this experiment was to prepare 2-butanone from 2-butanol. Chromic acid was used in this experiment to in order to prepare 2-butanol. Cr (VI) is rather orange‚ but Cr (III) is dark green - therefore by oxidizing the alcohol (2-butanol)‚ an orange Cr (IV) is reduced to green. NMR and IR tests were taken to determine the result‚ and the crystallized derivative of
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Experiment 6 Title: Preparation of bis(acetylacetonato)copper(II) complex Objective: To synthesize the bis(acetyacetonato) copper(II) complex Theory/Background: All metal ions in solution are ’associated’ with water. The water molecules can also be weakly bonded or more strongly as a ligand to form a complex ion‚ and these can also present in solid ’hydrated’ salts of crystallization. E.g Copper(II) nitrate (Cu(NO3) 2.3H2O). A complex ion has a metal ion at its centre with a number
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Preparation and SN1 Reactivity of 2-Bromobutane Paul DeJong Department of Chemistry‚ Illinois State University‚ Normal‚ IL 61790-4160 Submitted: April 4‚ 2013 Introduction The purpose of part 1 of the lab is to prepare 2-Bromobutane using SN1 reactions. The purpose of part 2 of the lab is to determine the relative reactivity of alkyl halides under SN1 conditions. Results and Discussion The Overall Reaction The Proposed Mechanism Experimental Procedure To prepare
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Preparation and SN1 Reactivity of 2-Bromobutane Whitney Bellido Department of Chemistry‚ Illinois State University‚ Normal‚ IL 61790-4160 Submitted: April 4th‚ 2013 Introduction The overall goal of this experiment is to understand and be familiar of SN1 reactivity. We also learned how to prepare 2-Bromobutane by learning how to distill and extract this product from its organic layer. Finally‚ another goal was to specifically understand the relative reactivity of alkyl halides under SN1 conditions
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Southville of Foreign University Preparation‚ Cooking and Finishing of Poultry Dishes A Report Researched to the Faculty of the School Of Hospitality Management In Partial Fulfillment of the Requirements Submitted to: Mr. Toribio Villanueva Submitted by: Ramone T Unit 19: Preparation‚ Cooking and Finishing of Poultry Dishes Know how to cook poultry for basic dishes (19.2.0) A. State the correct temperature for cooking poultry The correct temperature for cooking poultry is needed to ensure
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BMA 253 Intermediate Accounting Assignment #2 PART I Directions: 1) Complete the table below. 2) Calculate the estimated bad debts using aging of receivables method. Age Balance 1-60 days 61-120 days 121-180 days Over 180 days $80‚000 Probability Uncollectible of Default 2% $70‚000 4% $40‚000 8% $32‚000 11% Total PART II Directions: 1) Calculate the inventory cost for both periodic and perpetual method LIFO and FIFO using the following information and table below to fill in the shaded
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2012 Test Preparation Guide Entry-Level Special Agent Selection U.S. Drug Enforcement Administration Version 2.0 Revised June 2012 Table of Contents Introduction ....................................................................................... 1 Purpose of the Guide ................................................................... 1 Organization of the Guide ............................................................ 1 Section I: Overview of the Selection Process ...................
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