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Choose the major product of the following elimination. Please explain why the correct answer is letter C. Include detailed steps and a drawing explaining the mechanism of the reaction.
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- Draww all possible organic products and kinds of reactions (SN1, SN2, E1, E2)Draw all of the substitution and elimination products formed from thegiven alkyl halide with each reagent: (a) CH3OH; (b) KOH. Indicate thestereochemistry around the stereogenic centers present in the products,as well as the mechanism by which each product is formed.Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor product. (a) Draw a stepwise mechanism that shows how this alkene is formed. (b) Draw other alkenes formed in this dehydration. At least one must contain a ve-membered ring.
- Draw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3I; (b) TsCl and pyridine, followed by NaOCH3; (c) PBr3, followed by NaOCH3. Which two routes produce identical products?(c) ECH H₂ Pd/C (d) CH₂C=CCH₂CH₂ + D₂ Draw the product of reaction (c). Incorrect Lindlar catalyst N Draw the product of reaction (d). H1,2-Diols are converted to carbonyl compounds when treated with strong acids, in a reaction called the pinacol rearrangement. (a) Draw a stepwise mechanism for this reaction. (Hint: The reaction proceeds by way of carbocation intermediates.) (b) Assuming that the pinacol rearrangement occurs via the more stable carbocation, draw the rearrangement product formed from diol D.
- 1,2-Diols are converted to carbonyl compounds when treated with strongacids, in a reaction called the pinacol rearrangement. (a) Draw a stepwisemechanism for this reaction. (Hint: The reaction proceeds by way ofcarbocation intermediates.) (b) Assuming that the pinacol rearrangementoccurs via the more stable carbocation, draw the rearrangement productformed from diol D.Name the following aldehydes and ketones:For alkenes A, B, C, and D: (a) Rank A—D in order of increasing heat ofhydrogenation; (b) rank A—D in order of increasing rate of reaction withH2, Pd-C; (c) draw the products formed when each alkene is treated withozone, followed by Zn, H2O.