1. Please name the following compounds. (9 points) Br CI Br Br CI 2. Please draw the major product(s) of the following reaction and show the mechanism. Is there a reason why one stereochemistry is preferred over the other for this reaction? (9 points)

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### Organic Chemistry: Compound Naming and Reaction Mechanisms

#### Question 1

Please name the following compounds. (9 points)

**Compound Structures:**
1. A compound featuring two bromine atoms attached to a carbon chain that includes two double bonds.
2. A benzene ring with a bromine atom and an isopropyl group attached to it.
3. A benzene ring with a formyl group (CHO) and two chlorine atoms attached to it.

#### Question 2

Please draw the major product(s) of the following reaction and show the mechanism. Is there a reason why one stereochemistry is preferred over the other for this reaction? (9 points)

**Reaction Components:**
- A benzene ring.
- A compound with two carbonyl groups and a double bond (possibly maleic anhydride or a similar structure).

**Mechanism Explanation:**
- Discuss the reaction mechanism and any transition states or intermediates.
- Explain why one stereochemistry might be preferred over another, considering factors such as steric hindrance, electronic effects, or reaction kinetics.

Please provide detailed drawings and explanations for full credit.
Transcribed Image Text:### Organic Chemistry: Compound Naming and Reaction Mechanisms #### Question 1 Please name the following compounds. (9 points) **Compound Structures:** 1. A compound featuring two bromine atoms attached to a carbon chain that includes two double bonds. 2. A benzene ring with a bromine atom and an isopropyl group attached to it. 3. A benzene ring with a formyl group (CHO) and two chlorine atoms attached to it. #### Question 2 Please draw the major product(s) of the following reaction and show the mechanism. Is there a reason why one stereochemistry is preferred over the other for this reaction? (9 points) **Reaction Components:** - A benzene ring. - A compound with two carbonyl groups and a double bond (possibly maleic anhydride or a similar structure). **Mechanism Explanation:** - Discuss the reaction mechanism and any transition states or intermediates. - Explain why one stereochemistry might be preferred over another, considering factors such as steric hindrance, electronic effects, or reaction kinetics. Please provide detailed drawings and explanations for full credit.
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