Consider a reaction where cis-hex-3-ene is treated with Oso followed by NaHSO₂/H₂O.

The following two reactions are performed on the same starting material; one producing “product 1" and one producing "product 2" as the major products. Which of the following statements is false regarding these two reactions? Both of these reactions proceed A via a carbocation intermediate. Product 1 is a substitution В product. The leaving group in the reaction producing product 2 is H20. C Product 2 is a disubstituted alkene. Both of these reactions proceed E via a unimolecular reaction mechanism. он HCI (conc.) Product 1 (Major) он H2SO4 (conc.) Product 2 (Major)

Draw the product of the following sequence of reactions. Show stereochemistry.

Give the monoalkylation product for the following reaction.

Draw the major organic product of the reaction. Indicate the stereochemistry via wedge‑and‑dash bonds, including explicit HH and DD atoms, at the stereogenic center. Omit byproducts such as salts or methanol.

Draw TWO tautomers of cyclohexa-2,4-dienone A. Place arrows between the three structures and indicate which is the most thermodynamically stable isomeric form and why. A

2-bromo-2-methylbutane with sodium methoxide under SN2/E2 conditions substitution product elimination product both substitution and elimination products no products

Draw the major organic product of the indicated reaction conditions. Be sure to clearly depict the geometry of the product by correctly showing stereochemistry at stereocenters. H2, Pd BaSO4 H2N° CH3

This is not A or C. The second one is not A or D

Give the product of the following reaction, showing stereochemistry. NaCI CH;OH