Draw the Zaitsev product formed when 2,3-dimethylpentan-3-ol undergoes an E1 dehydration. Select Draw Rings More Erase H CH3 Е1 +H,0 HO. H3PO4
Analyzing Infrared Spectra
The electromagnetic radiation or frequency is classified into radio-waves, micro-waves, infrared, visible, ultraviolet, X-rays and gamma rays. The infrared spectra emission refers to the portion between the visible and the microwave areas of electromagnetic spectrum. This spectral area is usually divided into three parts, near infrared (14,290 – 4000 cm-1), mid infrared (4000 – 400 cm-1), and far infrared (700 – 200 cm-1), respectively. The number set is the number of the wave (cm-1).
IR Spectrum Of Cyclohexanone
It is the analysis of the structure of cyclohexaone using IR data interpretation.
IR Spectrum Of Anisole
Interpretation of anisole using IR spectrum obtained from IR analysis.
IR Spectroscopy
Infrared (IR) or vibrational spectroscopy is a method used for analyzing the particle's vibratory transformations. This is one of the very popular spectroscopic approaches employed by inorganic as well as organic laboratories because it is helpful in evaluating and distinguishing the frameworks of the molecules. The infra-red spectroscopy process or procedure is carried out using a tool called an infrared spectrometer to obtain an infrared spectral (or spectrophotometer).
![### Title: Formation of the Zaitsev Product from 2,3-dimethylpentan-3-ol
#### Objective:
To understand the process of forming the Zaitsev product when 2,3-dimethylpentan-3-ol undergoes an E1 dehydration reaction.
#### Reaction Details:
- **Reactant:** 2,3-dimethylpentan-3-ol
- **Reagent:** H₃PO₄ (phosphoric acid)
- **Condition:** E1 (Unimolecular Elimination) dehydration
#### Explanation:
The image displays a molecular structure for 2,3-dimethylpentan-3-ol. The structure shows:
- A six-membered carbon chain with a hydroxyl group (OH) attached to the third carbon.
- Two methyl groups are attached to the second and third carbons.
An arrow indicates the reaction proceeds in the presence of H₃PO₄, leading to the formation of a double bond, resulting in water (H₂O) as a byproduct.
#### Process:
1. **Protonation:** The hydroxyl group gets protonated by phosphoric acid.
2. **Formation of Carbocation:** Loss of water forms a carbocation at the tertiary carbon.
3. **Deprotonation:** The most substituted (stable) alkene forms, following Zaitsev's rule, where the hydrogen is removed from the adjacent carbon, resulting in a double bond.
#### Diagram Interface:
- **Tools:**
- Drawing tools for single and double bonds
- Element selection for carbon (C) and hydrogen (H)
- Features to undo/redo actions and zoom in/out
This interactive interface allows students to practice drawing the molecular structure and visualize the product of the reaction, reinforcing their understanding of E1 dehydration and Zaitsev's rule.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ffd2593c2-2536-47e2-82ef-fd438db56d59%2Fe6dc848a-253f-454e-88e7-775cb25efd89%2F0csf6mp_processed.png&w=3840&q=75)
![](/static/compass_v2/shared-icons/check-mark.png)
Trending now
This is a popular solution!
Step by step
Solved in 2 steps with 2 images
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Chemistry: Principles and Reactions](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Elementary Principles of Chemical Processes, Bind…](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)