Q6. Fill in the blanks left in each of the following syntheses: Example: OH H Find the flaw(s): ОН бл H₂O* H CH3OH, H H ОН ОН Emco H CO OCH3 H MgBr NHANH КОН ОН оньсо H₂CO OCH3 H
Q6. Fill in the blanks left in each of the following syntheses: Example: OH H Find the flaw(s): ОН бл H₂O* H CH3OH, H H ОН ОН Emco H CO OCH3 H MgBr NHANH КОН ОН оньсо H₂CO OCH3 H
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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![The image depicts a chemistry problem related to organic synthesis, specifically focusing on identifying errors in the synthetic pathway.
**Text:**
Q6. Fill in the blanks left in each of the following syntheses:
**Example:**
[Reaction pathway not described]
**Find the flaw(s):**
1. The initial compound is a cyclic ketone.
- Reagent: \( \text{H}_3\text{O}^+ \)
- Product: Cyclic alcohol derived from the ketone.
2. The cyclic alcohol undergoes a reaction:
- Reagent: \( \text{CH}_3\text{OH}, \:\text{H}^+ \)
- Resulting in a cyclic acetal formation.
3. A separate sequence involves:
- Reagent: \( \text{CH}_3\text{MgBr} \) (Grignard reagent)
- Product: An alcohol with additional carbon groups.
4. Further transformation includes:
- Reagents: \( \text{NH}_2\text{NH}_2, \:\text{KOH} \)
- Intermediate compound: Contains a carbonyl derivative reacting under these conditions.
The sequence involves reactive transformations such as hydration, acetal formation, and Grignard addition, and requires careful analysis to identify any possible errors in the chemical processes or logical flow.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F85c0b379-a78e-4342-b66b-7fce6e0a60cc%2Fa3f0b65a-c8f5-45d7-96f3-888a22a73009%2F9yygtge_processed.jpeg&w=3840&q=75)
Transcribed Image Text:The image depicts a chemistry problem related to organic synthesis, specifically focusing on identifying errors in the synthetic pathway.
**Text:**
Q6. Fill in the blanks left in each of the following syntheses:
**Example:**
[Reaction pathway not described]
**Find the flaw(s):**
1. The initial compound is a cyclic ketone.
- Reagent: \( \text{H}_3\text{O}^+ \)
- Product: Cyclic alcohol derived from the ketone.
2. The cyclic alcohol undergoes a reaction:
- Reagent: \( \text{CH}_3\text{OH}, \:\text{H}^+ \)
- Resulting in a cyclic acetal formation.
3. A separate sequence involves:
- Reagent: \( \text{CH}_3\text{MgBr} \) (Grignard reagent)
- Product: An alcohol with additional carbon groups.
4. Further transformation includes:
- Reagents: \( \text{NH}_2\text{NH}_2, \:\text{KOH} \)
- Intermediate compound: Contains a carbonyl derivative reacting under these conditions.
The sequence involves reactive transformations such as hydration, acetal formation, and Grignard addition, and requires careful analysis to identify any possible errors in the chemical processes or logical flow.
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