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- Determine 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 + CH3CH₂OHDraw a plausible mechanism for the reaction shown below. Et Ме OH ..Me 1) Excess EtMgBr 2) Hо Et "CIcat. H2 Ph CF3 Me0OC. .COOME Ph. -O H. please provide mechanism
- O 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 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 ♡ > Ր
- ! (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)?
- Draw complete mechanism (including intermediates) for each polar reaction below.Q5. Draw the all products and a detailed mechanism for the following reaction? -OCH2CH3 Br CH3CH2OHtempt.php?attempt3D1101388&cmid%3D371560 Draw a detailed mechanism showing the formation of all products, be sure to draw all intermediate and show the movement of electros by arrows. F. -Br -OCH3 -OCH3 Heat A - BI a