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![b. Please provide a "curved arrow" mechanism for the following transformation.
OH
H+
Браон
-OH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fbaf76a48-8ddd-420d-ac95-c89dc032d590%2F5feb19d1-d358-4c41-80a7-ee721d457330%2F2qgfna6_processed.jpeg&w=3840&q=75)
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- Provide a detailed, stepwise mechanism for the reaction shown below. CH3OH CH3 heat CH33. Provide a complete arrow pushing mechanism for the following transformation. H b HO NaOH heatDraw a stepwise mechanism for the following substitution. Explain why 2-chloropyridine reacts faster than chlorobenzene in this type of reaction.
- Q2. When (CH3CH2)3CBR is added to CH3OH at room temperature, the major product is (CH30)C(CH2CH3)3 and a minor product is CH3CH3DC(CH2CH3)2. Propose a mechanism for the product that is formed by the substitution reaction. Use curved arrows to show the movement of electrons.Q4. The herbicide oxyfluorfen can be prepared by the reaction between phenol and an aryl fluoride. Propose a curved arrow mechanism for this reaction. 1 F3C. LOCH2CH3 F3C. КОН CI `NO2 CI OH LOCH2CH3 `NO2 OxyfluorfenProvide a stepwise mechanism for the following reaction. F3C. F3C. KOC(CH3)3 CI но
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