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
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
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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b. 
c. 
d. 
**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.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff4bad56a-42cf-4354-a699-f947a893672e%2F372890a6-960d-4e60-bf82-1d3ba7932bc0%2Fl9kc14e_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Question 11:**
What product would you expect to obtain from the addition of Cl₂ to 1,2-dimethyl-cyclohexene?
Options:
a. 
b. 
c. 
d. 
**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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