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- The reaction of Hbr with 2-methylpropene produces 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction?Describe a sequence of reactions by which trans-2-pentene can be prepared from propyne.2-chloropropane is a major product of the reaction of chlorine with propane under ultraviolet light. Write the mechanism for this reaction including the initiation step and the two propagation steps.
- a) What products would you expect from the elimination reaction of 3-Bromo-2- methylpentane? Show the reaction by writing the condensed structural formula of the reactants and products. Identify the major and minor products. b) What alkyl halide might the 3,6-Dimethyl-1- heptene have been made from?The major product formed when methylenecyclohexane is treated with NBS in dichloromethane is 1-(bromomethyl)cyclohexene. Account for the formation of this product.2. Alcohols Write the complete step-by-step mechanism for the reaction of 3-methyl-2-pentanol with sulfuric acid.
- The acid-catalyzed dehydration of 2,3-dimethyl-3-pentanol yields three alkene products. What are the names of the three alkenes? Which of the three alkenes is the major product?What is the structure of the principal organic product formed in the reaction of 1-iodopropane with NaOH?Ethane reacts with chlorine (Cl2) in the presence of ultra-violet (UV) light, to produce 1-chloropropane (CH3CH2Cl) and hydrogen bromide (HCl). As shown in the equation below. CH3CH3 + Cl2 → CH3CH2Cl + HCl Describe the reaction mechanism of the reaction between ethane and chlorine to produce 1-chloroethane. The description should be detailed and must include the type of bond fission that takes place