Relative Reactivity of Alkyl Halides Introduction Nucleophilic substitution of alkyl halides can proceed by two different mechanisms – the SN2 and the SN1. The purpose of the experiment was to identify the effects that the alkyl group and the halide-leaving group have on the rates of SN1 reactions‚ and the effect that the solvent has on the rates of SN1 and SN2 reactions. The SN1 mechanism is a two-step nucleophilic substitution‚ or unimolecular displacement. In the first step of the mechanism
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Reactivity’s of Some Alkyl Halides- SN2 & SN1 A. Johnson 8/28/12 CHM236 Objective: To test the ten compounds found in the physical data table that follows‚ and observe them by categorizing the reactions as Sn1 and SN2. Physical data: Compound M.W. (g/mol) Melting Point (C°) Boiling Point (C°) Density (g/mL) Solubility Safety Considerations 2-chlorobutane 92.57 -140 68 0.87 very slightly soluble in cold water Irritant with skin‚ lung‚ and eyes. 2-bromobutane
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INTRODUCTION TO ASCLEPIAS CALIFORNICA The terrestrial plant‚ Asclepias californica‚ is the primary food source for Monarch butterflies. It can only germinate and produce seeds if provided with the proper environmental influence. The California milkweed’s population is spread out in the southern and coastal areas of California where there are flat lands and grassy slopes. It can also grow up to three feet tall and have clumps consisting of multiple stems that are a couple of feet in width. Unlike
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Experiment 1: Preparation of 1-Bromobutane and Reactivity of Alkyl Halides Objective: The purpose of this lab is to prepare 1-bromobutane from 1-butanol in an acid-catalyzed substitution reaction. While the reaction would be expected to occur as SN2 due to the primary nature of the substrate‚ because H2SO4 is used as a solvent‚ the conditions are very polar and the reaction can proceed via an SN1 reaction. The main objective is to obtain test results to determine the mechanism of the reaction
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Objective To compare the relative reactivities of different alkyl halides with two different reagents; sodium iodide in acetone and silver nitrate in ethanol. Below the reaction equations 1. RX+NAIRI+NAX (X=Cl or Br) in the presence of acetone 2. RX+AgNO3+EtOHROEt+AgX+HNO3 We used three substrates primary secondary and tertiary compounds are 1-bromobutane‚ 2-bromobutane and 2-bromo-2-methylpropane respectively to react with the two nucleophiles that are sodium iodide with acetone solvent and
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ASynthesis of an alkyl halide Jade A. Chuahiong and Marika Bianca F. Morioka Institute of Chemistry‚ University of the Philippines‚ Diliman‚ Quezon City 1101 Philippines Date Performed: April 25‚ 2013; Date Submitted: April 30‚ 2013 Alkyl halides could be synthesized through several processes and using different compounds as reactants. One of the simplest method used is the addition of a hydrogen halide to an alcohol. In this research‚ tert-butyl alcohol was reacted with cold concentrated
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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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SYNTHESIS OF AN ALKYL HALIDE S.M. BLANCAFLOR1 1INSTITUTE OF BIOLOGY‚ COLLEGE OF SCIENCE UNIVERSITY OF THE PHILIPPINES‚ DILIMAN‚ QUEZON CITY 1101‚ PHILIPPINES DATE SUBMITTED: 3 JANUARY 2012 DATE PERFORMED: 8 DECEMBER 2011 ------------------------------------------------- ABSTRACT Alkyl halides are molecules which have a carbon atom attached to a halogen atom (e.g.‚ chlorine‚ iodine‚ or bromine.) Alkyl halides are very important since they are used in many of the products used today
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Synthesis of an Alkyl Halide Maria Alexandria Buraga Ammuyutan Institute of Chemistry‚ University of the Philippines‚ Diliman‚ Quezon City 1101 Philippines ------------------------------------------------- Department of Food and Science Nutrition‚ College of Home Economics‚ Univeristy of the Philippines‚ Diliman‚ Quezon City 1101 Philippines ------------------------------------------------- ABSTRACT ------------------------------------------------- Alcohols react with hydrogen halides (HCl is
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Conversion of Alcohols to Alkyl Halides Ankita Patel August 6‚ 2013 Introduction This lab consisted of the conversion of alcohols into alkyl halides through common substitution methods. These methods include SN1 and SN2 mechanism‚ both of which can occur for this type of reaction. For both reactions‚ the first step of protonation will be to add hydrogen to the –OH group and then the rest of the reaction will proceed according to the type of mechanism. SN1 reactions form a cation intermediate
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