Tollowing two reactiOHS 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 H2O. C Product 2 is a disubstituted alkene. Both of these reactions proceed via a unimolecular reaction mechanism. он HCI (conc.) Product 1 (Major) он H2SO. (conc.) Product 2 (Major)

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1.Draw a structural formula for the more stable carbocation intermediate formed in the reaction shown. 2.Draw a structural formula for the major organic product of the reaction shown.

A novel heterocyclic compound, M, contains nitrogen and sulfur atoms and exhibits interesting photochemical properties. When exposed to ultraviolet (UV) light at a specific wavelength, M undergoes a photoreaction resulting in two products: N and O. Product N is formed through a [2+2] cycloaddition involving the nitrogen atom in M, while product O results from a homolytic cleavage of a sulfur-sulfur bond in M. Given these reaction pathways, what is the most probable structure of M, and what are the likely structures of N and O? A. M is a thiazole derivative; N is a dimerized product through the nitrogen atoms, and O is a compound with two sulfur-centered radicals. B. M is a diazine derivative; N is a tetra-atomic cyclic compound, and O is a compound with two separate thiol groups. C. M is a thiadiazole derivative; N is a four-membered ring involving the nitrogen atom, and O results in two sulfur-centered radicals. D. M is a dithiolane derivative; N is a dimer involving the nitrogen…