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- Plastic 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)?OChem reaction scheme help... Please provide the structures for the products obtained in the reaction schemes shown in the attaced image(b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants, the transition state, andthe products. Note that the initial product is the salt of an amine (RNH3+ Br - ), which is deprotonated by the excess ammonia to give the amine.
- What carbon radical is formed by homolysis of the C–Ha bond inpropylbenzene? Draw all reasonable resonance structures for thisradical.The replacement of CH3OH to dimethyl sulfoxide, DMSO (CH3)2S=O) as a solvent in the substitution reaction below results in what?Draw the mechanism fot his reaction. B = [IrCl(CO)(PPH3)2]
- Pls ignore the highlighted part __________ is reduced in thefollowing reaction: Cr2O72- + 6S2O32-+ 14H+→ 2Cr3+ + 3S4O62- + 7H2OThere are two isomeric cyclohexa-1,4-diene products when benzoic acid undergoes the Birch reduction (see Problem 25.24). (a) Draw the mechanism that leads tothe formation of the major product. (b) Will the Birchreduction of benzoic acid occur faster or slower than theBirch reduction of benzene itself? Hint: Is –CO2H anelectron-donating or an electron-withdrawing group?Draw the organic product(s) of reaction of the alkyne above with H3O+ in the presence of HgSO4.