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A: Given,
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- (b) What happens when- (i) is fast treated with CH3 H3CCO3H and then the product. obtained is anhydride (provide mechanism); treated with aceticProvide the product and mechanism and justify regiochemistry .CI Но- ofProvide to llaving Br a detailed, step by step mechanism for the reaction OCH₂CH3₂ OCH₂CH3 OCH₂ CH3
- Explain the mechanism of the reaction oxidizing from cyclohexanol to cyclohexanone. Explain detailed.Predict the product (s) with the appropri ate regio and stereochemical outcom e and provide a curved arrow mechanism for the reaction shown (hint: isopropanol reacts with intermediate) Cl, ? IsopropanolWhich of the following are a major product of the reaction sequence shown belo (1) Br2, FeBr3 (2) Mg/ether он он (A) (B) (3) (4) dil H* /H;O (C) (D) он Compound C Compounds B and D OCompounds A and B Compound D
- With sulfides are treated with α,β-unsaturated ketones and aldehydes, they can attackeither through direct or conjugate addition. Based on the NMR spectrum obtained fromthe product of the reaction below, indicate whether the reaction occurs by direct orconjugate addition and provide an arrow pushing mechanism(a) Provide a detailed mechanism for the reaction below. Explain any selectivity issues that arise. Ms = ---S -Me OMS CI + PhMgBr .CI1. Give the mechanism. He 아
- Provide the major organic product of the reaction below explain the mechanismHow can you distinguish in a SNAr reactionwhether it will occur according to an additionelimination or an elimination-addition mechanism?please provide the missing organic materials starting materials, reagents/reactions, conditions or organic products in the reaction below. kindly provide and show ther eaction mechanism as well