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- Do you know the product of the reaction?? thanksPlastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside the lenses that occurs when the lenses are exposed to sunlight. The original dye absorbs UV light but not visible light and is thus colorless, while the rearrangement product absorbs visible light and is thus darkened. (a) Show the mechanism of the rearrangement. (b) Why does the rearrangement product absorb at a longer wavelength (visible light) than the original dye (UV)?Which cycloaddition reaction will proceed the FASTEST? Select one: CHO OHC. CH3 CHO ||
- For the following reaction: Explain how to decide which mechanism(s) the reaction will follow including information about: o alkyl halide substitution (what type and what this tells you about the preferred mechanism) o nucleophile or base strength o solvent (what type and how this affects the mechanism) State which mechanism(s) will occur.". Draw the mechanism. Draw the product(s). *Which of the following is the MAJOR product of the following reaction? ... NaOEt ELOH Br ... (A OEtI want maknaism for this reaction!?
- The best reagent(s) for this reaction is/are ???Draw the final product of this series of reactions. |||** OH 1. SOCI₂ 2. NaCN • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one product is possible, only draw the major product. • If the reaction produces a racemic mixture, draw both stereoisomers.write the magor producb formed by the to llow ung eaction, Assume that You have enough of each rea Reactant to dvive the veaction bo Completion. Assume bhet thore i's protic wek up alone as neee ssary agont/ cl