QUESTION 11 What product would you expect to obtain from addition of C12 to 1,2-dimethyl-cyclohexene? a. a b d CI CI b. ac 'CI C. CI 11 d. CI ...l ••| CI

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**Question 11:**

What product would you expect to obtain from the addition of Cl₂ to 1,2-dimethyl-cyclohexene?

Options:

a. ![Option a](a represents a cyclohexane ring with two chlorine atoms attached to adjacent carbons in a vicinal dihalide manner.)

b. ![Option b](b illustrates a cyclohexane ring with one chlorine atom attached to a carbon above the plane and another hydrogen bond directing downward.)

c. ![Option c](c shows a cyclohexane ring with two chlorine atoms attached with one above and one below the plane of the ring.)

d. ![Option d](d is similar to c but with a different stereochemical orientation of chlorine atoms on the cyclohexane ring.)

**Explanation of Options:**

- **Option a** represents a syn addition where both chlorine atoms are added to the same side of the former double bond.
- **Option b** depicts an addition with different stereochemistry, with one chlorine atom above and a bond oriented downward.
- **Options c and d** both illustrate anti addition, where chlorine atoms are added to opposite sides of the double bond, but differ based on the orientation of stereochemistry. 

**Overall Reaction Details:**

The addition of Cl₂ to an alkene such as 1,2-dimethyl-cyclohexene typically leads to anti addition due to the mechanism of halogenation, resulting in dihalides. The final products often have stereochemistry determined by the halogenation reaction pathway.
Transcribed Image Text:**Question 11:** What product would you expect to obtain from the addition of Cl₂ to 1,2-dimethyl-cyclohexene? Options: a. ![Option a](a represents a cyclohexane ring with two chlorine atoms attached to adjacent carbons in a vicinal dihalide manner.) b. ![Option b](b illustrates a cyclohexane ring with one chlorine atom attached to a carbon above the plane and another hydrogen bond directing downward.) c. ![Option c](c shows a cyclohexane ring with two chlorine atoms attached with one above and one below the plane of the ring.) d. ![Option d](d is similar to c but with a different stereochemical orientation of chlorine atoms on the cyclohexane ring.) **Explanation of Options:** - **Option a** represents a syn addition where both chlorine atoms are added to the same side of the former double bond. - **Option b** depicts an addition with different stereochemistry, with one chlorine atom above and a bond oriented downward. - **Options c and d** both illustrate anti addition, where chlorine atoms are added to opposite sides of the double bond, but differ based on the orientation of stereochemistry. **Overall Reaction Details:** The addition of Cl₂ to an alkene such as 1,2-dimethyl-cyclohexene typically leads to anti addition due to the mechanism of halogenation, resulting in dihalides. The final products often have stereochemistry determined by the halogenation reaction pathway.
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