(a) Explain with suggestive mechanism why BuLi undergoes 1,2-addition with a, B- unsaturated ketones, whereas Me,CuLi undergoes 1,4-addition with the same.
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- Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .(A) Provide the major organic product for the reaction below (B) Would the product be optically active of optically in active?OChem help... Complete the following reaction sequence: Indicate regiochemical/stereochemical details as relevant. Provide the stepwise mechanism for the following... (see image)
- Hydrogenation of alkene A with D2 in the presence of Pd-C affords a single product B. Keeping this result in mind, what compound is formed whenA is treated with each reagent: (a) mCPBA; (b) Br2, H2O followed by base? Explain these results.Give a clear handwritten answer with explanation needed!! Give the mechanism of given bleow reactions with curved arrows and formal changes with explanation..?Which reaction below give a par of diastereomers and Why?
- Friedel–Crafts alkylation of benzene with (R)-2-chlorobutane and AlCl3 affords sec-butylbenzene.a. How many stereogenic centers are present in the product?b. Would you expect the product to exhibit optical activity? Explain, with reference to the mechanism.Provide the mechanism of the redica reaction below (b)- Identify compounds J & K - Draw a curved arrow mechanism that accounts for the formation of J (take into account stereochemical considerations)
- The following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.Hydrogenation of alkene A with D2 in the presence of Pd-C affords a single product B. Keeping this result in mind, what compound is formed when A is treated with each reagent: (a) mCPBA; (b) Br2, H2O followed by base? Explain these results.give in dept mechanism of structures A and B