Provide a detailed mechanism for the transformation shown. Remember to show all steps. OH H3PO4, A What type of general reaction occurs in the last step of the transformation above? Write out your answer, take a picture, and embed it as an image using the following steps.
Provide a detailed mechanism for the transformation shown. Remember to show all steps. OH H3PO4, A What type of general reaction occurs in the last step of the transformation above? Write out your answer, take a picture, and embed it as an image using the following steps.
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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![### Detailed Mechanism for the Transformation Reaction
#### Description
The image presents a chemical transformation where a cyclohexanol derivative is converted into a cyclohexene derivative under the influence of phosphoric acid (H₃PO₄) and heat (Δ).
#### Provided Reaction Scheme
- Reactants: A cyclohexanol derivative.
- Reagent/Conditions: H₃PO₄, Δ (phosphoric acid and heat).
- Product: A cyclohexene derivative.
### Explanation and Key Points:
The main reactant is a cyclohexanol derivative featuring an -OH group attached to a secondary carbon in the cyclohexane ring. Under the conditions of H₃PO₄ (phosphoric acid) and heat, this substance undergoes a dehydration reaction to form a double bond, resulting in a cyclohexene derivative.
#### General Reaction Type
The general reaction is a **dehydration reaction**. This type of reaction involves the elimination of a water molecule from the reactant, facilitated by an acid catalyst and heat, leading to the formation of an alkene.
### Instructions for Students:
1. **Provide a detailed mechanism**:
- Begin with the protonation of the hydroxyl group by phosphoric acid.
- Show the formation of the carbocation intermediate after the loss of water.
- Illustrate the rearrangement, if any, and the final elimination step resulting in the formation of the double bond.
2. **Answer the question about the type of general reaction**: Identify it as a dehydration reaction.
3. **Document your answer**: Write it out, take a picture, and embed it as an image using the following steps.
#### Steps to Embed an Image:
1. Write down the detailed mechanism showing all steps thoroughly.
2. Take a clear picture of your handwritten work.
3. Embed the image in the designated section in your assignment submission following the platform-specific instructions provided.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F6e82c55c-6f4e-499d-87a7-ae36525c0cfd%2F6d12c378-99e5-44ff-8b44-130f0b592b6d%2F1ubgmi_processed.png&w=3840&q=75)
Transcribed Image Text:### Detailed Mechanism for the Transformation Reaction
#### Description
The image presents a chemical transformation where a cyclohexanol derivative is converted into a cyclohexene derivative under the influence of phosphoric acid (H₃PO₄) and heat (Δ).
#### Provided Reaction Scheme
- Reactants: A cyclohexanol derivative.
- Reagent/Conditions: H₃PO₄, Δ (phosphoric acid and heat).
- Product: A cyclohexene derivative.
### Explanation and Key Points:
The main reactant is a cyclohexanol derivative featuring an -OH group attached to a secondary carbon in the cyclohexane ring. Under the conditions of H₃PO₄ (phosphoric acid) and heat, this substance undergoes a dehydration reaction to form a double bond, resulting in a cyclohexene derivative.
#### General Reaction Type
The general reaction is a **dehydration reaction**. This type of reaction involves the elimination of a water molecule from the reactant, facilitated by an acid catalyst and heat, leading to the formation of an alkene.
### Instructions for Students:
1. **Provide a detailed mechanism**:
- Begin with the protonation of the hydroxyl group by phosphoric acid.
- Show the formation of the carbocation intermediate after the loss of water.
- Illustrate the rearrangement, if any, and the final elimination step resulting in the formation of the double bond.
2. **Answer the question about the type of general reaction**: Identify it as a dehydration reaction.
3. **Document your answer**: Write it out, take a picture, and embed it as an image using the following steps.
#### Steps to Embed an Image:
1. Write down the detailed mechanism showing all steps thoroughly.
2. Take a clear picture of your handwritten work.
3. Embed the image in the designated section in your assignment submission following the platform-specific instructions provided.
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