Synthesis Of Bromination Of Stilbene Dibromide
Bromination is the process where an alkene is halogenated with bromine. The purpose of this experiment was bromination of stilbene to stilbene dibromide. The element bromine is toxic and requires maximum care when used. Bromine was generated in the reaction mixture by using a green method. Less hazardous reagents were used to do so. This can be seen by the chemical reaction 2HBr+H_2 O_2→〖Br〗_2+2H_2 O. Hydrogen peroxide is used to oxidize HBr to 〖Br〗_2. By adding hydrogen peroxide this can make working with bromine less dangerous. This experiment is a greener approach to the bromination process because ethanol was used as a solvent. Ethanol is nontoxic making the experiment less harmful. 0.5202g of stilbene and 10mL of ethanol were added
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1125 Words | 5 PagesThis was proved by utilizing the IR spectrum to verify the C =O was not in the final product as it lacked the 1640 cm-1 peak. The melting point of 113-115 degrees C proved that the final product obtained was the E-Stilbene. The TLC plate proved that the E and the Z product was produced, show cased by the double intensity of the DCM spot to the final product’s spot, both which had an Rf of 0.92. The double intensity proved that both products were produced, but through heating and filtering, the Z-Stilbene was
Esterification Of Butyl Ethanoate Lab Report
1261 Words | 6 PagesThe two reactants present in the esterification process are the functional groups; carboxylic acid and alcohol. This reaction can be catalysed by the presence of H+ ions, often sulphuric acid is used. This type of esterification, where carboxylic acid and alcohol with an acid catalyst are used is known as the Fischer esterification. This is the type of esterification process which will be undertaken within this experiment, where 4mL of concentrated sulphuric acid will be used to speed up the reaction. It is also important to note that the esterification reaction can also include reactions of; an acyl halide
Julia Brown
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1-Bromobutane Lab Report
704 Words | 3 PagesAs relayed in Table 1, the results concluded that the only molecules to react and form a precipitate were 1-chlorobutane and 1-bromobutane. 1-bromobutane formed a precipitate first, after two minutes and eight seconds. 1-cholorobutane did not for a precipitate until after heat was applied after seven minutes and fifty-one seconds. 2-cholorbutane, 2-bromobutane, and tert-butyl-chloride did not react at all during the course of the experiment. 1-bromobutane was expected to react first, followed by 1-chlorbutane.
Potassium Bromate Lab Report
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Oxopentanoic Acid Synthesis Lab Report
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Lab Report: Nitration Of Bromomobenzene
1022 Words | 5 PagesLab Report 10: Nitration of Bromobenzene Raekwon Filmore CM 244 Section 40 March 27, 2018 Introduction: For this experiment, nitration of bromobenzene was the focus of the lab. The benzene is an aromatic compound and when it reacts with wither a mixture of sulfuric acid or nitric acid creates what is known as a nitro group.
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1468 Words | 6 PagesMany other chlorinated and brominated aromatic compounds such as tryptophan, tyrosine and many other derivatives of pyrrole are also present in nature. Reactions of haloarenes or reactions of aryl halides can be primarily divided into three types: Nucleophilic Substitution Reactions Electrophilic Substitution Reactions Reaction with Metals The reaction of Haloarenes – Nucleophilic Substitution Reactions
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