Bromination of trans- Stilbene to form 1‚2- Dibromo- 1‚2-diphenylethane Abstract 1‚2-dibromo-1‚2-diphenylethane was produced by the bromination of trans-stilbene through the addition of hydrobromic acid (HBr) and hydrogen peroxide (H2O2). This experiment was a greener bromination of stilbene because bromine was generated in situ and ethanol was used as the solvent. The melting point (243.30°C)‚ mass (.427g)‚ and percent yield (45.54) of the crystals were recorded. The FTIR
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Mikkelson‚ A. C.‚ Hesse‚ C.‚ & Pauley‚ P. M. (2007). Affectionate writing reduces total cholesterol: Two randomized‚ controlled trials. Human Communication Research‚ 33‚ 119-142. In the article‚ “Affectionate Writing Reduces Total Cholesterol: Two Randomized‚ Controlled Trials‚” the authors set out to show that writing down affectionate thoughts about close family and friends can reduce your total cholesterol levels. They continue by stating that one can find mention of affection in almost all studies
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Preparation of 4-bromoaniline Introduction Aromatic compounds tend to undergo electrophilic aromatic substitutions rather than addition reactions. Substitution of a new group for a hydrogen atom takes place via a resonance-stabilized carbocation. As the benzene ring is quite electron-rich‚ it almost always behaves as a nucleophile in a reaction which means the substitution on benzene occurs by the addition of an electrophile. Substituted benzenes tend to react at predictable positions. Alkyl groups
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The Stereochemistry of Bromine Addition: Bromination of trans-Cinnamic Acid Pitak Chuawong Objectives 1. To perform bromination of trans-‐cinnamic acid 2. To investigate stereochemistry of bromination reaction Introduction Alkenes undergo electrophilic addition to give alkyl halides. When bromine is used as a
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properties of the hydrocarbons. Several reactions such as Bromination‚ oxidation‚ and the addition of sulfuric acid were done to understand the chemical properties as well as the possible products that may form by each of the classification of hydrocarbons. Preparation of acetylene was also done in this experiment. The properties of the formed acetylene such as the reaction of the acetylene as it undergo Ammoniacal silver nitrate test‚ Bromination and oxidation. The reagents that were used to perform
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REACTIONS OF HYDROCARBONS Vanessa P. Manibpel De La Salle University - Dasmariñas ABSTRACT Five substances namely Hexane‚ Eugenol‚ Unknown hydrocarbon 1‚ Unknown hydrocarbon 2‚ and Acetylene gas was used for the selective reactivity of hydrocarbons to functional group tests; Bayer’s test‚ Bromine test light‚ Bromine test dark‚ and Tollen’s test. In Bayer’s test‚ only Acetylene‚ Eugenol and Unknown hydrocarbon 2 reacted positively and the rest retain the purplish color of KMnO4. On the other hand
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considered “greener” compared to the original bromination procedures. In order to create the alkyl halides‚ which are able to undergo chemical transformations more readily than the carbon-carbon double bond‚ onto the trans-stilbene the addition process of halogenation in needed. The typical reagents that are used‚ such as elemental bromine and liquid bromine‚ are dangerous and highly corrosive‚ so this experiment used an alternative method of bromination.
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Marta Gebregziabher Discussion and Conclusion: Addition reaction of Alkenes: Bromination of (E)-Stilbene 1. Addition reaction is a reaction that involved two molecules that combine to make a larger product. Addition reaction has two main types‚ electrophilic addition and nucleophilic addition. An electrophilic reaction is when the pi bond of a molecule is removed to make two covalent bonds that are bonded to two new molecules. A nucleophillic addition is a reaction that removed the pi bond
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chemistry experiment involved carrying out the first three parts of the Cyclohexanol Cycle. The cyclohexanol was first converted to cyclohexene and water by simple distillation (product: 6.5395g‚ 79.75% recovery). The cyclohexene then underwent a bromination reaction by addition of concentrated HBr and a 30% H2O2 solution‚ followed by an extraction of the aqueous phase. This produced trans-1‚2-dibromocyclohexane (product: 12.8886g‚ 67.34% recovery). The trans-1‚2-dibromocyclohexane was reduced by zinc
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Bromination of Trans-Cinnamic Acid Christopher B. Martin CHEM 3411 1 Mechanism of Bromine Addition to Alkenes Understanding the chemical mechanism (order of bonds broken and made as well as intermediates formed) has a great value in chemical synthesis. The chemical mechanism of a reaction will influence the rate of the reaction‚ the stereochemistry of the product(s)‚ and the extent of possible undesired side reactions. Organic reaction mechanisms investigate the path towards a desired product
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