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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What is the IUPAC name for this molecule?
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
Transcribed Image Text:### Ocimene - Structural Representation
**Chemical Structure:**
The image depicts the structural formula of Ocimene, a monoterpene. It is represented by a sequence of carbon and hydrogen atoms arranged in a chain with three double bonds.
**Description:**
- **Carbon Atoms (C):** The backbone is a series of interconnected carbon atoms.
- **Hydrogen Atoms (H):** Each carbon atom bonds with hydrogen atoms. The chemical formula typically balances each carbon's valence needs.
- **Double Bonds:** There are three double bonds in the structure, indicating locations of unsaturation within the hydrocarbon chain.
**Notation:**
- **CH₃ and CH₂:** These denote the methyl and methylene groups attached to the main carbon chain.
- **Bonds and Angles:** The structure illustrates the angles and linear arrangements typical in organic chemistry depictions, indicating sp² hybridization at double bond sites.
This structure is a trans isomer of Ocimene, commonly found in nature and known for its fragrant properties.
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