The molecule below can be synthesized via two pathways using the SN2 reaction through the formation of the C-S bond. For each retrosynthetic pathway, draw the nucleophile and electrophile and choose with pathway would be more efficient and explain why
The molecule below can be synthesized via two pathways using the SN2 reaction through the formation of the C-S bond. For each retrosynthetic pathway, draw the nucleophile and electrophile and choose with pathway would be more efficient and explain why
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 molecule below can be synthesized via two pathways using the SN2 reaction through
the formation of the C-S bond. For each retrosynthetic pathway, draw the nucleophile and
electrophile and choose with pathway would be more efficient and explain why

Transcribed Image Text:### Chemical Structure: Thioanisole
**Molecular Formula:** C9H10S
**Description:**
This chemical structure represents Thioanisole, a simple aromatic organic compound with the molecular formula C9H10S. It consists of a benzene ring attached to a sulfur atom, which is further connected to a methyl group.
**Diagram Explanation:**
- **Benzene Ring:** The left side of the diagram shows a hexagonal ring, which represents a benzene ring composed of six carbon atoms with alternating double bonds.
- **Sulfur Atom (S):** Attached to the benzene ring is a sulfur atom, depicted by the letter 'S'.
- **Methyl Group:** Attached to the sulfur is a chain ending in a methyl group (CH3), representing the alkyl chain in Thioanisole.
This structure is utilized in various chemical reactions and serves as an intermediate in the synthesis of other compounds.
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