Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm³¹ ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrometry (not shown): [M] = 88 m/z Infrared Spectroscopy (not shown): 3376, 2967, 2927 cm¹ ¹H Nuclear Magnetic Resonance. 5 1H 1³C Nuclear Magnetic Resonance. 80 8 60 50 3 PPM 40 PPM 30 2H 6H 3H 20 10
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).
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![**Information:** Each spectrum below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm⁻¹.
¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a “zoom-in” on an important part of the spectrum.
**Mass Spectrometry (not shown):** [M] = 88 m/z
**Infrared Spectroscopy (not shown):** 3376, 2967, 2927 cm⁻¹
**¹H Nuclear Magnetic Resonance:**
- A graph is displayed with the chemical shift (PPM) on the x-axis ranging from 0 to 5 PPM.
- Signals:
- A singlet (s) at approximately 3.4 PPM, integrating to 1 hydrogen.
- A quartet (q) at around 1.2 PPM, integrating to 2 hydrogens.
- A triplet (t) at about 0.9 PPM, integrating to 3 hydrogens.
**¹³C Nuclear Magnetic Resonance:**
- A graph is shown with the chemical shift (PPM) on the x-axis ranging from 0 to 80 PPM.
- Peaks are observed at:
- Approximately 13, 25, 41, and 72 PPM.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa451162e-14ac-4cfd-a2c6-1eae7f4a5f1a%2Fa0e4a63f-f07c-49ae-b826-b1731547fc5b%2Fzwt1nn_processed.png&w=3840&q=75)
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