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- cat. H2 Ph CF3 Me0OC. .COOME Ph. -O H. please provide mechanismDetermine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OH! ( plz explain and give mechanism , I will upvote )
- ↑ ... Propose a reasonable stepwise mechanism, using curved arrow notation to show the flow of electrons, for the following reaction. KCN H EtOH, H₂O OH 02N O₂N NO2 Tt O ọ ♡ > ՐO wnich one of the followng will mos+ undevgo nucleophil ic ViO the addition- elimina +ian pathuoy with avomotie Sub stilution Socd um methoxide ? e) b)! (plz give ans with mechansim/ explanation where ever you can , plz try to do mechanism , i will upvote )
- Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate arrows, intermediates, and formal charges. HO H2SO4 (cat.) HO refluxPlastic 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)?Q5. Draw the all products and a detailed mechanism for the following reaction? -OCH2CH3 Br CH3CH2OH
- Draw complete mechanism (including intermediates) for each polar reaction below.propose a Cómplete mechanism for the reattions shown below all curved arrows aud intermediates , including Me HO, Conc. H2SO4A student attempted to synthesize an epoxide according to the reaction scheme shown here, but no epoxide was formed. Explain why. Hint: It may be helpful to build a OH NaOH No epoxide model of the reactant molecule. (H3C);C' Br
