#10 **Draw the organic product of the reaction.**In the given reaction, the starting materials are a cyclohexyl iodide compound and an isopropoxide ion (\(-OCH(CH_3)_2\)). The reaction implies a substitution, where the iodide (I) group on the cyclohexane is replaced by the isopropoxide group.- **Reactants:** - Cyclohexane ring with an attached iodide group. - Isopropoxide ion (\(-OCH(CH_3)_2\)).- **Task:** - Draw the resulting organic product in the provided space.The dashed box labeled "draw structure ..." is intended for users to sketch the structure of the reaction product.**Explanation for Educational Context:**This activity involves understanding nucleophilic substitution reactions, where a nucleophile (isopropoxide ion) replaces a leaving group (iodide) in an organic compound, typical of SN2 reactions. This enhances the understanding of reaction mechanisms and organic synthesis.

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Draw the organic product of the reaction. draw structure + -OCH(CH3)2

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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Concept explainers

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.

Question

#10

**Draw the organic product of the reaction.**

In the given reaction, the starting materials are a cyclohexyl iodide compound and an isopropoxide ion (\(-OCH(CH_3)_2\)). The reaction implies a substitution, where the iodide (I) group on the cyclohexane is replaced by the isopropoxide group.

- **Reactants:**
- Cyclohexane ring with an attached iodide group.
- Isopropoxide ion (\(-OCH(CH_3)_2\)).

- **Task:**
- Draw the resulting organic product in the provided space.

The dashed box labeled "draw structure ..." is intended for users to sketch the structure of the reaction product.

**Explanation for Educational Context:**

This activity involves understanding nucleophilic substitution reactions, where a nucleophile (isopropoxide ion) replaces a leaving group (iodide) in an organic compound, typical of SN2 reactions. This enhances the understanding of reaction mechanisms and organic synthesis.

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