Draw the structural formula(s) for the major product(s) of each of the following reactions. Unless required, ignore stereochemical details

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Draw the structural formula(s) for the major product(s) of each of the following reactions. Unless required, ignore stereochemical details
**(j)**

- **Reactants**: 
  - A methylcyclohexene compound
  - Methanol (\(CH_3OH\))

- **Arrow and Conditions**: The reaction is carried out in the presence of sulfuric acid (\(H_2SO_4\)).

- **Description**: This is likely an acid-catalyzed reaction involving the addition of methanol to the double bond of the cyclohexene ring, possibly resulting in an ether formation.

---

**(k)**

- **Reactants**: 
  - A methylcyclopentene compound
  - Acetic acid (\(CH_3COOH\))

- **Arrow**: The reaction proceeds in one direction with no additional reagents explicitly mentioned.

- **Description**: This may represent an esterification or similar reaction involving the addition of the acetic acid to the alkene, potentially forming an acetate ester derivative.

---

**(l)**

- **Reactants**: 
  - Cyclohexene 
  - Trifluoroacetoxymercury acetate \((CF_3COO)_2Hg\) in methanol (\(CH_3OH\))

- **Conditions**: Followed by the addition of sodium borohydride (\(NaBH_4\)).

- **Description**: This sequence likely represents an oxymercuration-demercuration process. Initially, the alkene undergoes oxymercuration forming an organomercury intermediate, which is then reduced by sodium borohydride to yield an alcohol.
Transcribed Image Text:**(j)** - **Reactants**: - A methylcyclohexene compound - Methanol (\(CH_3OH\)) - **Arrow and Conditions**: The reaction is carried out in the presence of sulfuric acid (\(H_2SO_4\)). - **Description**: This is likely an acid-catalyzed reaction involving the addition of methanol to the double bond of the cyclohexene ring, possibly resulting in an ether formation. --- **(k)** - **Reactants**: - A methylcyclopentene compound - Acetic acid (\(CH_3COOH\)) - **Arrow**: The reaction proceeds in one direction with no additional reagents explicitly mentioned. - **Description**: This may represent an esterification or similar reaction involving the addition of the acetic acid to the alkene, potentially forming an acetate ester derivative. --- **(l)** - **Reactants**: - Cyclohexene - Trifluoroacetoxymercury acetate \((CF_3COO)_2Hg\) in methanol (\(CH_3OH\)) - **Conditions**: Followed by the addition of sodium borohydride (\(NaBH_4\)). - **Description**: This sequence likely represents an oxymercuration-demercuration process. Initially, the alkene undergoes oxymercuration forming an organomercury intermediate, which is then reduced by sodium borohydride to yield an alcohol.
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