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Write the reaction for the formation of 1,4-di-t-butyl-2,5-dimethoxybenzene.
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- What product is formed from the hydrogenation of 2-methylpropene?What is the biological reducing agent that gives rise to the formation of chiral ethyl 3-hydroxybutanoate?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?
- Draw the structure of 4,6-Diethyl-3-methyl-3-octanol. Then, name the product that you would expect to produce by its oxidation.Give the reagent and the reaction conditions that would distinguish between the following compounds. Explain the principles behind the reactions. Write the chemical equation for the reactions involved. 3-ethyl-2iodopentane and 3-bromo-4-tert-butyl-1-heptene.Identify the type of reaction for the formation of (S)-2-butanol from (S)-2-bromobutane
- Write an equation for the reaction of chloroacetic acid (Ka=1.5103) with trimethylamine (Kb=5.9105) . Calculate the equilibrium constant for the reaction. If 0.10 M solutions of these two species are mixed, what will be their concentrations at equilibrium?When the conjugate acid of aniline, C6H5NH3+, reacts with the acetate ion, the following reaction takes place: C6H5NH3+(aq)+CH3COO(aq)C6H5NH2(aq)+CH3COOH(aq) If Kafor C6H5NH3+ is 1.35105 and Kafor CH3COOH is 1.86105 , what is K for the reaction?The reaction of Hbr with 2-methylpropene produces 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction?
- What function does sulfuric acid have in the reaction with 1-butanol to form 1-bromobutane?What is the chemical equation involved with the reaction of cyclohexene with Br2?When trans-2-chloro-1-cyclohexanol is treated with a base, cyclohexene oxide is the product. However, when cis-2-chloro-1-cyclohexanol is treated with a base, the product is cyclohexanone i. Write the equation for the reaction between trans-2-chloro-1-cyclohexanol and the base to yield the cyclohexene oxide. ii. Why doesn’t the cis isomer yield the oxide?. iii. Write the mechanism for each of the two reactions.