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- In this reaction with bromine, monosubstitution of lakane A forms a mixture of organic product. Show the structures of two monosubstituted organic products that are formed.Draw the alkyl bromide and the nucleophilemethanol + CH3OH Suppose you were told that the above reaction was a substitution reaction but you were not told the mechanism. Evaluate the following categories to determine the reaction mechanism and then draw the structure of the major organic product. Type of alkyl halide: Type of nucleophile: Solvent: Is the product racemic?
- See image belowQ7 Consider the reaction, where the alkane shown is subjected to radical bromination at 25 °C. Br₂ light Describe the major monobromination product. productThe Wolff–Kishner reaction uses hydrazine (H2NNH2) and hydroxide (–OH) to reduce a carbonyl to the alkane. The first steps of the mechanism convert a carbonyl to a hydrazone in a manner similar to imine formation. Draw the mechanism arrows for the reaction from the hydrazone to the alkane. Be sure to add lone pairs of electrons and nonzero formal charges to all species.
- The reaction of 1-bromobutane with sodium hydroxide affords the substitution product butan-1-ol. What would happen to the rate of the reaction if the concentration of both 1-bromobutane and sodium hydroxide were doubled? The rate increases by a factor of 4. The rate decreases by a factor of 2. The rate remains the same. The rate increases by a factor of 2.In the following electrophilic aromatic substitution reaction, the major product results in the substitution occurring at the 2 position. Starting from each potential carbocation intermediate shown, (a) draw the possible resonance structures and (b) explain why the major product is favored. Br 4 Br2 5 Br major product minor product + Br Br 2. LO1. Predict the product, and propose a mechanism for the following nucleophilic addition to aldehyde or ketone. Are the products different from one another? Why do the reactions proceed via different mechanisms? Note the charges on the intermediates of acid and base catalyzed reactions. Oxygen nucleophile in acidic condition H2O, [H+] Oxygen nucleophile in basic condition NaOH
- C12T02Q7080 Give the major product of the following reaction. 1) NaBH4 2) H30+ H. HO. There is no reaction under these conditions or the correct product is not shown here. HO.Draw the major and minor neutral organic products that would form when the alkene below undergoes acid-catalyzed hydration. ignore the stereochemistry, so your two products should be regioisomers.Topic: Elimination of Alkyl Halides When 2-bromobutane is reacted with CH3O-, two alkene products, namely 2-butene and 1-butene are obtained. Give an explanation why the E2 reaction produces 2-butene as the major product