Predict the organic and inorganic products of the given reaction, and select the class to which the product belongs. Then, complete the curved-arrow mechanism. i H + H H N Q2Q Draw the organic and inorganic products. N H H - H
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- How many different organic products are possible when pentan-2-ol is heated in the presence of acid? Ignore any stereoisomers (cis/trans isomers).organic chemistry 1) The product of the following reaction is:Formulate the major organic product of the following reaction of 4‑chloro‑4‑methyl‑1‑pentanol in neutral polar solution. Draw the product. The product has a molecular formula of C6H12O.
- Alkyl sulfonates undergo the same type of substitution reactions as alkyl halides and can also be prepared from alcohols. What advantage does the preparation of an alkyl sulfonate from an alcohol have over the preparation of an alkyl halide from an alcohol?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?Write the reagent or draw structures of the starting material or organic product(s) in the following reactions. If more than one product is formed, identify the major product where possible. (a) (b) HO OH OH H2SO4 ? Cl₂ ? FeCl3
- Describe a sequence of reactions by which cis-2-pentene could be prepared from acetylene.Esterication is the reaction of a carboxylic acid (RCOOH) with an alcohol (R'OH) to form an ester (RCOOR') with loss of water. Equation [1] is an example of an intermolecular esterication reaction. Equation [2] is an example of an intramolecular esterication reaction; that is, the carboxylic acid and alcohol are contained in the same starting material, forming a cyclic ester as product. The equilibrium constants for both reactions are given. Explain why Keq is different for these two apparently similar reactions.Draw the organic product obtained by hydroboration-oxidation of each of the following alkenes: (a) trans-2-pentene, (b) 2-tert-butyl-3,3-dimethyl-1- butene, and (c) 1-methylcyclohexene. Having done this, draw the product of the acid-catalyzed hydration of these same alkenes. How do the reaction products differ?
- 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?Predict the major organic product for the following reactions Draw the condensed structural formulas for the reactants and products and name the products (organic compounds only) If there is no reaction write NR. If a compound is a hemiacetal or acetal, don't name it – just label it as "hemiacetal" or “acctal." a) 2-methyl-3-pentanone + 2-propanol (isopropyl alcohol) b) Product in (a) + 2-butanol c) Complete oxidation of 3,4-dimethyl-1-pentanol (strong oxidizing agent) d) Hydration of 1,3-dimethylcyclopentene ) Intermolecular dehydration of 2-methyl-1-propanol (isobutyl alcohol)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?