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- Which compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaFDraw the ALL of the E2 organic product formed when the structure shown below undergoes dehydrohalogenation in KOH with heat.Draw the major organic product you would expect to isolate from the reaction of p-bromoethoxybenzene with a misture of HNO3HNO3 and H2SO4H2SO4.
- Explain why Jone's oxidation of 4-methyl-2-pentanol is faster than that of 3,3-dimethyl-2-pentanol.Why is this considered an Elimination E2 reaction? C₃H₈O (l) → C3H6 (g) + H2O (l) propan-1-ol → propene + waterDraw the structure of the product of the reaction between the compound shown below and H2SO4.
- Which one of the statements below is wrong about Zaitsev’s Rule. a. None of the above b. The Zaitsev’s Rule demonstrate the principle of regioselectivity in elimination reactions c. The more substituted alkene is the major product of E1 or E2 elimination d. The more substituted alkane product is obtained when a proton is removed from β-carbon that is bonded to the fewest hydrogens e. The most stable alkene is generally the major productShow the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.Draw the major organic product of the SN1SN1 reaction: