Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction Unknown Letter: B 23 April 2013 Academic Integrity Statement: “Experimental data may be collected with other students in organic chemistry labs. However I understand that sharing information required for a lab report (including but not limited to word processing or spreadsheet files‚ calculations‚ graphs‚ conclusions and additional problems at the end of the lab report) with other students is a violation of the University
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Title: Relativities of Alkyl Halides in Nucleophilic Substitution Reactions Introduction: The purpose of this lab was to perform a comparison of relative reactivities of various alkyl halides with two different reagents‚ sodium iodine in acetone and silver nitrate in ethanol. (Below are the reaction equations). We used different substrates‚ which were primary‚ secondary‚ and tertiary. These substrates included 2-bromobutane‚ 2-bromo-2-methylpropane‚ 1-bromobutane ∞-Bromotoluene‚ bromobenzene
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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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Experiment 21: Reaction of some Akyl Halides Completed on November 13‚ 2012 Purpose The purpose of this experiment was to examine reactiveness of 10 organic compounds under both SN1 and SN2 conditions. Table of Chemicals Compound Structure Molecular Weight (g/ml) Boiling Point (°C) Melting Point (°C) Density (g/ml) Safety 1-bromobutane 137.03 102 -112 1.269 Flammable‚ irritant 2-chloro-2-methylpropane 92.57 51 -26 0.89 Flammable‚ irritant acetone 58.08 56.5 -95 0.793 flammable
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3/22/2012 ARYL HALIDES 2. displacement reactions of diazonium salts ARYL HALIDES General formula: Ar–X where X = F‚ Cl‚ Br or I Examples Structure: C-X bonds are shorter and stronger Bond C-Cl C-Br Ar-X 1.69 A° 1.86 A° R-X 1.77 1.91 Dipole moments are unusually small. Bond C-Cl Preparation: 1. electrophilic aromatic substitution – useful only if one product is obtained C-Br Ar-X 1.7 D 1.7 D R-X 2.10 D 2.15 D Dipole moments may cancel out depending on the geometry of the
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Reactivity of Halide Ions Michelle Faktor and Kelly Freas Date of Experiment: October 28‚ 2012 Period 2 Honors Chem Purpose: The purpose of this lab is to observe the reactions of halide ions with different reagents by mixing them together. Analyze data to determine characteristic reactions of each halide ion. Infer the identity of unknown solutions. Materials: * 0.1 M AgNo3 * 0.1 M NaCl * 0.1 M NaF * 0.2 M KBr * 0.2M Kl * 0.2 M Na2S2)3 * 0.5 M Ca(NO3)2
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CLASSIFICATION TESTS FOR ORGANIC HALIDES James Anand L. Regala‚ Sabrina Nicolle G. Sarte‚ Ann Michelle Siao‚ Michael Sibulo‚ Victoria Tan Group 8 2C Pharmacy Organic Chemistry Laboratory ABSTRACT This experiment is done to classify organic halides. Most organic halides are synthetic and are not flammable. One way to classify organic halides is by classifying its -carbon atom as primary‚ secondary or tertiary. If the -carbon is attached to one R group‚ it is then primary. If the -carbon is
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Reactivity of Halide Ions Purpose: There are four halide salts used in this experiment that are found in the human body. Sodium fluoride is poisonous‚ but has been traced to be beneficial to humans in the prevention of tooth decay. Sodium chloride is added to many of our foods to increase flavor. Sodium chloride is important for many life processes‚ but too much intake is linked to high blood pressure. Sodium bromide is distributed throughout body tissues. Sodium iodine controls cell growth. The
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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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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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