Which of the following reagents are appropriate for the transformation below A) PCC B) Ph3P=CHCH3 C) H₂NNH₂ / KOH D) HOCH₂CH₂OH/H+ E) CH3CH₂MgBr F) NaBH4 G) LiAlH4 ? घ
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).
![The image consists of a chemical reaction involving two structures and a list of options to consider.
On the left, there is a ketone structure with the molecular formula representing a 2-pentanone, involving a carbonyl group (C=O) attached to a five-carbon chain.
In the middle, there is an arrow with a question mark, indicating an unknown reaction process.
On the right, a linear structure is shown, representing a hydrocarbon chain, specifically pentane.
Below the reaction scheme, there are five options indicated by circles with letters:
- A
- B
- C
- F
- G
These options likely refer to possible reagents or conditions that could result in the depicted transformation from a ketone to an alkane. The task is to select the correct option that facilitates this transformation.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F3570e46f-30e2-426f-a164-b9f03cf8994f%2Fc7dbdf9d-ce86-4bce-87e8-0bd9b497775b%2Fchc0cyh_processed.jpeg&w=3840&q=75)
![**Question:**
Which of the following reagents are appropriate for the transformation below?
A) PCC
B) \( \text{Ph}_3\text{P}=\text{CHCH}_3 \)
C) \( \text{H}_2\text{NNH}_2 / \text{KOH} \)
D) \( \text{HOCH}_2\text{CH}_2\text{OH} / \text{H}^+ \)
E) \( \text{CH}_3\text{CH}_2\text{MgBr} \)
F) \( \text{NaBH}_4 \)
G) \( \text{LiAlH}_4 \)
**Transformation Diagram:**
The diagram shows a structural transformation. On the left, there is a ketone with a five-carbon skeleton, specifically 2-pentanone. An arrow indicates the transformation. On the right side, there is a linear structure representing pentane, a five-carbon alkane. The question marks above the arrow suggest the need to identify a suitable reagent to achieve this transformation from a ketone to an alkane.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F3570e46f-30e2-426f-a164-b9f03cf8994f%2Fc7dbdf9d-ce86-4bce-87e8-0bd9b497775b%2Fxwooofs_processed.jpeg&w=3840&q=75)
![](/static/compass_v2/shared-icons/check-mark.png)
Trending now
This is a popular solution!
Step by step
Solved in 3 steps with 1 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)