*5% Carbocation Rearrangements 7) Draw the 5 MOST LIKELY carbocation rearrangements of the following intermediate. Bonus: Put an X next to the least likely structure and briefly explain why. H ok
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- What reaction out of each pair is faster?????Draw the equilibrium chair confirmation of cis1-chloro-3-methylcyclohexane. Interpret the E2 elimination, and draw the structure of the product!The reaction shown can give two different mono-alkylation products depending on the conditions. Draw the kinetic and thermodynamic products of the reaction. 1. base Kinetic + Thermodynamic Products 2. CH3CH₂Br (1 equiv.) Draw the kinetic product. Draw the thermodynamic product. Select Draw Rings More Erase Select Draw Rings More Erase / ||| ||| C H O / || III C H O
- 2) Use your understanding of reaction rates to identify the faster reaction for each of the following pairings. HC Br O CECH Br 2 equiv of OR H NH2 Br 2 equiv of ONH2 BrUse the following reaction coordinate diagram to answer the following four questio Consider only the forward reaction. a. Which step is the fastest? b. Which step is the slowest? c. Which step is the most exergonic? d. Which compound will the first transition state appear most like? Free Energy Progress of rxn D EThe product of this first step is called a "tetrahedral intermediate." Click on its structure. Ö: :0 H3C-C-O-CH3 Ī CH3 H₂C C :O-CH3 :OH H3C-C-O-CH3 :O-CH3 :0 H₂C-C-OH :O-CH3 +H H H3C-C-O :O-CH3