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- best condition for the reaction (1r,2s)-1 bromo-2methylcyclohexane->(s)3-methylcyclohex-1eneWhat is the structure/s of the major organic product/s for the reaction below?cmplete the reacting by adding necessrt reagents. write in thapce provided. make sure to write regents in chemical formula . n separate regents with comma & space (ex. h2so6, h202)
- draw a table showing selection rule for m+n cycloaddition and cyclo reversion reactionsShow 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+ .The Predict the product.... b) Label any kinetic/thermodynamic produc... c) Give reason towards the selection of kinetic product....
- For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOCH3 in CH3OHChemistry Give the products of the reaction of 1 mole of 2-methy1-1,3-pentadiene with 1 mole of HBr. Whichproduct(s) will predominate if the reaction is under kinetic control? Which products) will predominateif the reaction is under thermodynamic control?Using differences in C-H bond dissociation energies, calculate approximate selectivities secondary vs primary halogenation for the following compouond at 0o C. Be sure to include numberical differences.
- a. Show that [4+4] cycloaddition of two butadiene molecules to give cycloocta-1,5-diene is thermally forbidden but photochemically allowed b.Thermally allowed cycloaddition of the two butadiene molecules when there's a different. Show reaction and explain why it is thermally allowCarbocations often rearrange, as shown below. Draw in the hydrogens on the two carbons involved in the rearrangement, and show formal arrow-pushing to illustrate the transformation.Elimination occurs when (Z)-3-bromohex-3-ene is treated with NaNH2. Under the same conditions, 1-bromocyclohexeneundergoes elimination much more sluggishly. Explain why