hybridization they have. The three main groups of Hydrocarbons are Alkanes‚ Alkenes‚ and Alkynes (1). Alkanes are sp3-hybridized hydrocarbons characterized by single bonds between carbon atoms included in their chains. Alkanes are also called saturated hydrocarbons because they contain the highest possible H atoms that they can since their single bonds give the Carbon atoms the opportunity to bond with three or two hydrogen atoms. Alkenes on the other hand are sp2-hybridized substances that are distinguished
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are compounds that only contain carbon and oxygen atoms. Alkanes‚ alkenes‚ alkynes and aromatic rings are the four classifications of hydrocarbons. Each of these classifications have different physical and chemical properties that were tested as this experiment was performed. Flammability test and solubility test were done to understand and compare the physical properties of the hydrocarbons. Several reactions such as Bromination‚ oxidation‚ and the addition of sulfuric acid were done to understand
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clear liquid. After adding 3 drops red 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
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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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equation. [3 marks] d) The quality assurance manager of the production plant found out that the method in (c) is not very efficient and has decided to look for an alternative pathway to produce nhexane. He suggested on forming an intermediate step of alkene‚ which later undergoes reduction reaction to form n-butane. Propose two reaction pathways to produce n-butane‚ writing the complete chemical reaction equations. [10 marks] e) n-hexane is a type of alkane. List three physical properties of alkane.
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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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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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phenol soln in test tube + 1 drop FeCl3 soln Aliphatic and Aromatic Hydrocarbons/ Alkenes Bromination in Light (Free Radical Bromination) (Reacts with alkanes) Reagent: Br2 in H2O Observation: decolorization‚ brown ( colorless Procedure: 2 drops of test compound in test tube+ 1 drop 0.05 M Br2 in H2O‚ shake well‚ record observations Bromination in Dark (Electrophilic Addition Halogenation) (Reacts with alkenes) Reagent: Br2 in H2O Observation: decolorization‚ brown ( colorless Procedure:
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form‚ write the structure of any meso compounds below. If none would form‚ write the word “NONE” below. [pic] 3. (25 points) The following reaction produces a major alkene product. First‚ on the Newman template provided draw the conformation from which the raction will occur. Then‚ on the product alkene template provided‚ draw the product that will form from this reaction. Finally‚ indicate the stereochemical designation of the major product.
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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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