a. D. O Mor + H. + H. O CI CI Pd(OAc)2 PPH3, NEt3 Pd(OAc)2 PPH3, NEt3

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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Answer this using betta hydride elimination and alkene stereochemistry.  What are the products for the following reactions? Be aware of alkene stereochemistry. 

### Chemical Reaction Transcription:

#### Reaction Scheme:

**a.** 

![Compound 1 Structure](#)
- **Chemical Structure Details:**
  - Left Component: An unsaturated ester with a phenyl group attached to a conjugated enone system.
  - Right Component: A benzaldehyde derivative with a chlorine substituent on the phenyl ring.

**b.**

![Compound 2 Structure](#)
- **Chemical Structure Details:**
  - Left Component: A simple α,β-unsaturated ester.
  - Right Component: Same as the right component in Reaction Scheme a.

#### Reaction Conditions:

- **Catalyst:** Pd(OAc)₂ (Palladium(II) acetate)
- **Ligands:** PPh₃ (Triphenylphosphine) and NEt₃ (Triethylamine)

### Explanation of Reaction Process:

This reaction involves coupling reactions likely facilitated by palladium catalysis, a commonly used method in organic chemistry to form carbon-carbon bonds. The use of ligands such as triphenylphosphine and bases such as triethylamine indicates a stabilization and activation process in the catalytic cycle. The chemical equation suggests a potential transformation involving aromatic or conjugated systems, which are often subjects of such palladium-catalyzed couplings.
Transcribed Image Text:### Chemical Reaction Transcription: #### Reaction Scheme: **a.** ![Compound 1 Structure](#) - **Chemical Structure Details:** - Left Component: An unsaturated ester with a phenyl group attached to a conjugated enone system. - Right Component: A benzaldehyde derivative with a chlorine substituent on the phenyl ring. **b.** ![Compound 2 Structure](#) - **Chemical Structure Details:** - Left Component: A simple α,β-unsaturated ester. - Right Component: Same as the right component in Reaction Scheme a. #### Reaction Conditions: - **Catalyst:** Pd(OAc)₂ (Palladium(II) acetate) - **Ligands:** PPh₃ (Triphenylphosphine) and NEt₃ (Triethylamine) ### Explanation of Reaction Process: This reaction involves coupling reactions likely facilitated by palladium catalysis, a commonly used method in organic chemistry to form carbon-carbon bonds. The use of ligands such as triphenylphosphine and bases such as triethylamine indicates a stabilization and activation process in the catalytic cycle. The chemical equation suggests a potential transformation involving aromatic or conjugated systems, which are often subjects of such palladium-catalyzed couplings.
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