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- ONZ IS ON Determine which substitution mechanism occurs and draw the products, including stereochemistry. + -OCH3 DMSO Br H + CH3OH Br CH,CH, CH3Dehydration 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.A) C) Predict the major product of the following transformation: .CO₂Et H₂O* Heat COET C₁0H 100 B) D)
- K96.Draw the structure of the major product of each reaction (If a racemic mixture is formed, indicate both enantiomers), and show the mechanismDehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tertbutylcyclopentene as a minor product. (a) Draw a stepwise mechanismthat shows how this alkene is formed. (b) Draw other alkenes formed inthis dehydration. At least one must contain a five-membered ring.
- (a) Draw all products formed by treatment of each dibromide (A and B) with one equivalent of NaNH2. (b) Label pairs of diastereomers and constitutional isomers. H Br H Br CH3 CH3 Br H H Br A2) Predict the major product for each reaction. Indicate correct stereochemistry. a. b. H3C H3C HO ||||| HO ||||| CH3 ||||| Br H Br CH3 H NaOH NaOH thrive qode-tums ng uboiqy4) Give the correct product with the correct stereochemistry. Me Me 5) Give the major product. hv HCI OC