1 Predich the Majar products(s) for thre reacticns below draw a mechanism fareach 2. Include labels for products Suchas Markovnikov or Anti-Markovnikov HBr HBr ROOR
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- Can you show me the mechanism for the following practice problem. Thank youIn addition to organic halides, alkyl tosylates (R′OTs) reactwith organocuprates (R2CuLi) to form coupling products R–R′. When 2°alkyl tosylates are used as starting materials (R2CHOTs), inversion of theconfiguration at a stereogenic center results. Keeping this in mind, drawthe product formed when each compound is treated with (CH3)2CuLi.Reaction of 2° alcohol A with HCl forms three alkyl chlorides, all of whichresult from rearrangement of the 2° carbocation initially formed. Draw thestructures of these products and a mechanism that illustrates how eachis formed.
- Propose reaction conditions (A) and draw the products (B, C and D) of each transformation. Curvedarrow mechanisms are not required.Please draw the mechanism (assuming an SN1pathway) for the reaction of cyclopentyl bromide with the cyanide anion (-CN) to yield cyclopentyl cyanide as the organic product Thank youPlastic 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)?
- Provide the curved arrow mechanism for the reaction of the compound shown below treated with Cl2/FeCl3. Include transition states and the major product. I apprecitate the helpDraw the mechanism ffrom benzaldehyde to this using: i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+, H2O1. SN1 or SN2 2. Include major product and stereochemistry 3. Add detailed reaction mechanisms
- For eaach image, predict the MAJOR product(s). Show stereochemistry where applicable and draw out ALL stereoisomers formed (as major products) in each reaction. State the mechanism(s) by which the major product(s) are formed (SN1, SN2, E1, and/or E2). Reagents are NOT present in excess.Do not give handwriting solution. please draw out what compound A is and then provide aroow pushing mechanism for thisreaction! thanks01 Cive the ctrientiono of Comnand 4 2.2 Provide a reasonable arrowpushing mechanism for the reaction in 2.1I need an explanation on the mechanism, linked bellow 1 paragraph explanation on the steps and mechanism. and what the final product is called