NaOCH3 Methanol Br Br Br KI Br Br sringkas viideie to 1sbo gricee

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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5. Complete the following reactions by writing the correct product:

Ph

\[ \underbrace{NaOCH_3} \]
Transcribed Image Text:5. Complete the following reactions by writing the correct product: Ph \[ \underbrace{NaOCH_3} \]
The image depicts four different chemical reactions involving brominated compounds.

1. **First Reaction:**
   - **Reactant:** A brominated compound where the bromine (Br) is attached to a carbon chain.
   - **Reagent:** Sodium methoxide (NaOCH₃) in methanol.
   - **Product:** The outcome of this reaction is not explicitly shown in the image.

2. **Second Reaction:**
   - **Reactant:** A compound with bromine attached as a side group.
   - **Reagent:** Potassium tert-butoxide (tBuOK) in tert-butanol (tBuOH).
   - **Product:** The reaction proceeds, but the specific product is not illustrated.

3. **Third Reaction:**
   - **Reactant:** A compound with two bromine atoms on adjacent carbon atoms.
   - **Reagent:** Potassium iodide (KI).
   - **Product:** The image suggests the reaction leads to the elimination of bromine, though the product is not fully visible.

4. **Fourth Reaction:**
   - **Reactant:** A bicyclic compound with two bromine atoms.
   - **Reagent:** Zinc (Zn) in acetic acid.
   - **Product:** The result of this reaction is also not depicted in detail.

These reactions suggest typical elimination and substitution reactions as seen in organic chemistry, often used to transform functional groups and study reaction mechanisms.
Transcribed Image Text:The image depicts four different chemical reactions involving brominated compounds. 1. **First Reaction:** - **Reactant:** A brominated compound where the bromine (Br) is attached to a carbon chain. - **Reagent:** Sodium methoxide (NaOCH₃) in methanol. - **Product:** The outcome of this reaction is not explicitly shown in the image. 2. **Second Reaction:** - **Reactant:** A compound with bromine attached as a side group. - **Reagent:** Potassium tert-butoxide (tBuOK) in tert-butanol (tBuOH). - **Product:** The reaction proceeds, but the specific product is not illustrated. 3. **Third Reaction:** - **Reactant:** A compound with two bromine atoms on adjacent carbon atoms. - **Reagent:** Potassium iodide (KI). - **Product:** The image suggests the reaction leads to the elimination of bromine, though the product is not fully visible. 4. **Fourth Reaction:** - **Reactant:** A bicyclic compound with two bromine atoms. - **Reagent:** Zinc (Zn) in acetic acid. - **Product:** The result of this reaction is also not depicted in detail. These reactions suggest typical elimination and substitution reactions as seen in organic chemistry, often used to transform functional groups and study reaction mechanisms.
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