Description If you ever painted a wall‚ then‚ you have encountered toluene. Toluene has many uses‚ and it is a chemical compound we use more often than we think. In this lesson‚ we will be learning all about toluene‚ which is an organic chemical compound. !!!Toluene: Structure and Formula Have you ever used or smelled paint thinners? If you have‚ then that is how we can describe the smell of toluene. Toluene is one of the ingredients used in manufacturing many commercial products‚ like paints
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SEPERATING CYCLOHEXANE AND TOLUENE BY DISTILLATION Aim: Separate two miscible liquids‚ either by macroscale or microscale process‚ using simple and fractional distillation. Compare the efficiencies of simple and fractional distillation. INTRODUCTION: The purpose of this experiment is to learn how to separate two miscible liquids by microscale process. There will be use of simple and fractional distillation. Simple and fractional distillation efficiencies will be compared. The student should have
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The purpose of the experiment was to perform an electrophilic addition reaction by the bromination of cinnamic acid. The product of this reaction is 3-Phenyl-2‚3-dibromo propionic acid‚ which is purified by recrystallization. Cinnamic acid (3-phenylprop-2-enoic acid) is an unsaturated carboxylic acid. The electron rich π cloud (see Figure 1) in the double bond of this structure is nucleophilic and can be considered a Lewis base. It can therefore be saturated by the addition of a halogen to the double
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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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27/September/2013 Experiment 3B: Fractional Semi-microscale Distillation Separation of Hexane and Toluene. Objective: The main goal of this lab is to learn how separation of binary liquid mixtures is performed. Especially when the two liquids have boiling points varying by about 30° C. Hexane can be separated from toluene in this experiment because of the difference in their boiling points. Since toluene has a higher boiling point‚ it will left at the bottom while the hexane starts to boil out and
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color Br2/CH2Cl 2 the solution turned orange. Orange color held. Alkene Alkene used was pentene. Originally clear liquid. After addition‚ solution turned yellowish at first but then turned clear after a few minutes of sitting. Alkyne Alkyne used was toluene. Originally clear liquid. After addition‚ solution turned orange. Orange maintained longer than alkene but eventually turned clear. Unknown Originally clear liquid. After addition of unknown‚ turned orange but eventually faded to clear color after
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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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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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Preparation and Characterization of Alkene Balacanao‚ Gladys A.1‚ Miranda‚ MarilynI2 1 Student (s)‚ Subject/Section‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology; 2 Professor‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology [pic] ABSTRACT The purpose of this experiment is to prepare cyclohexene form cyclohexanol‚ and know the properties of alkene. The first part of this experiment is preparation of cyclohexene
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Alkane‚ Alkene‚ Alkyne & Aromatic Learning Objectives 1. 2. 3. Determine the IUPAC name‚ common name and structure of an alkanes‚ alkenes and cycloalkanes. Identify the physical properties of alkanes. Describe briefly natural sources and importance of alkanes Describe reactions of alkanes Propose a mechanism on free radicals substitution 4. 5. 6. Describe the preparation and reactions of alkenes. 7. Propose mechanism on preparation; dehydration of alcohol 8. Define carbocation
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