Specify a synthetic scheme that would produce the compound shown above in the fewest steps possible. Use one of the starting materials shown together with any of the available reagents. Give the number of the starting material followed by the letters of the reagents in the order of their use, for example: 3be. Starting Materials сновановость снованван 1 2 Available Reagents a. CH₂I b. CH₂CH₂ C. d. Submit Answer e CH₂Br Br Br Retry Entire Group h. Br 3 O -COC₂H5 'Br i. NaOC₂H₂ J. H₂O*, heat or NaOH, H₂O; then H₂O*, heat 9 more group attempt Previous Next> Save and Exit
Specify a synthetic scheme that would produce the compound shown above in the fewest steps possible. Use one of the starting materials shown together with any of the available reagents. Give the number of the starting material followed by the letters of the reagents in the order of their use, for example: 3be. Starting Materials сновановость снованван 1 2 Available Reagents a. CH₂I b. CH₂CH₂ C. d. Submit Answer e CH₂Br Br Br Retry Entire Group h. Br 3 O -COC₂H5 'Br i. NaOC₂H₂ J. H₂O*, heat or NaOH, H₂O; then H₂O*, heat 9 more group attempt Previous Next> Save and Exit
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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Pick the reagent(s) and starting material that will produce this compound

Transcribed Image Text:### Synthesis Challenge
**Objective:**
Specify a synthetic scheme to produce the compound shown above in the fewest steps possible. Use one of the starting materials provided, along with any of the available reagents. Indicate your answer in the format: starting material number followed by the letters of the reagents used (e.g., 3be).
**Compound to be Synthesized:**
The target compound is a hexenone. The structure includes a cyclohexenone ring connected to a propene chain.
---
**Starting Materials:**
1. \( \text{C}_2\text{H}_5\text{OCCH}_2\text{COC}_2\text{H}_5 \)
2. \( \text{C}_2\text{H}_5\text{OCCH}_2\text{CH}_2 \)
3. Cyclohexanone ethyl ester
---
**Available Reagents:**
- a. \( \text{CH}_3\text{I} \)
- b. \( \text{CH}_3\text{CH}_2\text{I} \)
- c. Propyl iodide
- d. Butyl iodide
- e. Cyclohexyl bromide
- f. \( \text{Br}_2 \)
- g. Allyl bromide
- h. \( \text{Br}_2, \text{hv} \)
- i. Sodium ethoxide (NaOC\(_2\)H\(_5\))
- j. Acidic or Basic hydrolysis: \( \text{H}_3\text{O}^+, \text{heat} \) or \( \text{NaOH, H}_2\text{O}; \text{then} \text{H}_3\text{O}^+, \text{heat} \)
**Instructions:**
Select the most appropriate starting material and reagents to propose a concise synthetic route to obtain the target compound. Input your answer following the example format.
**Example Response Format:**
3be
Make sure to maximize efficiency and minimize the number of steps in the synthetic process.
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