Click Chemistry Reactions: An Experimental Study
In This reaction dimethyl acetylenedicarboxylate was used as the dienophile with a Carbonyl group as the electron-withdrawing group. A resonance stabilized aromatic ring was formed ( favored rection). The nitrobenzene was used to facilitate the by acting as a high boiling solvent, dissolving both reactants, and thereby driving the Diels-Alder reaction. Refluxing moved this reaction further, forming an intermediate. The violet solution turned beige when forming a six-membered ring by losing carbon monoxide.
The hypothesis was supported by the employed methods. Introduction: This experiment was performed to show how bromination of alkenes reacts, and to be able to successfully synthesize meso-stilbene dibromide. The reaction of bromine with alkenes is an addition reaction where the nucleophilic double bond attacks the electrophilic bromine
Many sources of error were responsible for recovering a small amount of product. Introduction: The carbon-carbon bond formation is an important tool in organic chemistry to construct the simple as well as an organic compound. There are several
Tyler White CHEM151LL 32658 04/01/2018 Different Types Chemical Reaction Types and Equations Purpose: The purpose of this lab experiment is to examine different types of chemical reactions such as Decomposition reaction, Synthesis reactions, Combustion reactions, and different Chemical equations. The experiments were conducted online using Late Nite Labs. Materials: Because the experiments were conducted online there wasn’t any physical use of materials, only digital ones, for these labs to be performed. Only the registration for the website was needed to perform these online labs, as well as a desktop computer.
Chem 51 LB Experiment 3 Report Scaffold: Bromination of Trans-Cinnamic Acid 1. The goal of this experiment was to perform a halogenation reaction through the addition of two bromides from pyridinium tribromide. This was accomplished by reacting trans-cinnamic acid with pyridinium tribromide. After the reaction took place, melting point analysis was conducted to find out the stereochemistry of the product, which could either be syn-addition, anti-addition, or syn + anti-addition. 2.
Experiment 2 Report Scaffold (Substitution Reactions, Purification, and Identification) Purpose/Introduction 1. A Sn2 reaction was conducted; this involved benzyl bromide, sodium hydroxide, an unknown compound and ethanol through reflux technique, mel-temp recordings, recrystallization, and analysis of TLC plates. 2. There was one unknown compound in the reaction that was later discovered after a series of techniques described above.
Grignard is a reaction that is crucial to forming the new carbon-carbon bond. This is a two-part lab that teaches new techniques; the purpose of this lab is to introduce realistic organic synthesis and apply acid workup to produce triphenylmethanol. A Grignard reaction is characterized by the addition of a magnesium halide (an organomagnesium halide) to an aldehyde or a ketone in order to form a secondary or tertiary alcohol. These reactions are helpful because they serve as a crucial tool in performing important carbon-carbon bond-forming reactions (Arizona State University, 2018). This experiment aimed to observe the mechanisms of a Grignard reply to synthesize triphenylmethanol from benzophenone using phenylmagnesium bromide as the Grignard reagent.
It is understood the mechanism is acid-catalyzed where protons coordinate with the carbonyl oxygen to make the carbonyl carbon more electropositive for nucleophilic attack (Scheme 1). In the experimental procedure all reactants were added together, this is inefficient as the protons can coordinate with either trans-cinnamic acid or methanol. Coordination with methanol is unnecessary as it reduces its nucleophilicity and makes less protons available to coordinate with the carboxylic acid. To improve
The Diels-Alder reaction, an electrocyclic reaction between a conjugated diene and a substituted alkene, also known as a dienophile, was used in the experiment. The purpose was to synthesize a substituted cyclohexene derivate by the reaction between the diene and dienophile, and it reacted in a reflux solution with toluene as the solvent forming an unsaturated six-membered ring. First, approximately 54 mg each of both compounds, tetraphenylcyclopentadienone (TPCPD) and diphenylacetylene (DPA), were placed in a reaction tube to be mixed and heated on a sand bath for several minutes. During the heating process, the color of the TPCPD reactant would fade as the color went from purple to white showing the other reactant. Also during the heating, DPA refluxed for a brief time until the tube was removed from the sand bath for the melted product to cool and solidify.
The goal of the experiment is to synthesize a bromohexane compound from 1-hexene and HBr(aq) under reflux conditions and use the silver nitrate and sodium iodide tests to determine if the product is a primary or secondary hydrocarbon. The heterogeneous reaction mixture contains 1-hexene, 48% HBr(aq), and tetrabutylammonium bromide and was heated to under reflux conditions. Heating under reflux means that the reaction mixture is heated at its boiling point so that the reaction can proceed at a faster rate. The attached reflux condenser allows volatile substances to return to the reaction flask so that no material is lost. Since alkenes are immiscible with concentrated HBr, tetrabutylammonium bromide is used as a phase-transfer catalyst.
One of the most used methods for the formation of six-membered rings is using the reactions of 1,3-diene with an alkene. The Diels-Alder reaction is a unique reaction in organic chemistry because it is a cycloaddition reaction. The Diels-Alder reactions are also known as 1,4 addition reactions due to the formation of new carbon-carbon σ bonds and π bonds. Electron-withdrawing groups like cyano (C≡N) and carbonyl (C=O) to increase the reaction rates and reaction yields (1). Often times there are no side reactions that occur during the Diels-Alder reactions.
The objective of the experiment completed was to form the product 9,10-dihydroanthracene-9,10-α,β-succinic anhydride from anthracene and maleic anhydride. The reaction that took place is named a Diels-Alder reaction, defined as an addition reaction in which a diene unites with a double or triple bond of an unsaturated compound to form a 6-membered-ring. The following reactions below depict the ways in which dienes and dienophiles join to form products. Anthracene functioned as a diene and maleic anhydride functioned as the dienophile. Xylene was used as a solvent that provided a quicker way of reaction between the two starting materials.
Aims of experiment • Determine the rate constants for hydrolysis of (CH3)3CCl in solvent mixtures of different composition (50/50 V/V isopropanol/water and 40/60 V/V isopropanol/water) • Examine the effect of solvent mixture composition on the rate of hydrolysis of (CH3)3CCl Introduction With t-butyl chloride, (CH3)3CCl, being a tertiary halogenoalkane, it is predicted that (CH3)3CCl reacts with water in a nucleophilic substitution reaction (SN1 mechanism), where Step 1 is the rate-determining step. The reaction proceeds in a manner as shown
Lecturer Date Introduction Theoretical Background Procedure The procedure was segmented into two categories, the reaction set up and the crude product isolation. Reaction set up The magnetic stirrer was prepared through placing it in the fume cupboard. 1 mmol of L-Phenylalanine was placed and weighed in a 5 mL conical vial.
Cyclopropane is a flammable, synthetic compound which is a ring made up of three carbon atoms. Each carbon atom has two stereoselective hydrogens thus creating a molecular formula of C3H6. Cyclopropane is seen in daily life through physiological activity and in chemical and biological transformations. Cyclopropanols are versatile building blocks for organic synthesis because of the ability to undergo various transformation. The unique ring structure, that involves an -OH group, allows for many opportunities for drug design in today’s pharmaceutical field, especially in antibiotics.
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