Infrared Spectroscopy An Instrumental Method for Detecting Functional Groups

Similar documents
Lecture 11. IR Theory. Next Class: Lecture Problem 4 due Thin-Layer Chromatography

Infrared Spectroscopy

Radiant energy is proportional to its frequency (cycles/s = Hz) as a wave (Amplitude is its height) Different types are classified by frequency or

Infrared Spectroscopy

More information can be found in Chapter 12 in your textbook for CHEM 3750/ 3770 and on pages in your laboratory manual.

C h a p t e r F o u r t e e n: Structure Determination: Mass Spectrometry and Infrared Spectroscopy

SPECTROSCOPY MEASURES THE INTERACTION BETWEEN LIGHT AND MATTER

ORGANIC - BROWN 8E CH INFRARED SPECTROSCOPY.

Symmetric Stretch: allows molecule to move through space

Infrared Spectroscopy

1.1. IR is part of electromagnetic spectrum between visible and microwave

Introduction. The analysis of the outcome of a reaction requires that we know the full structure of the products as well as the reactants

Infrared Spectroscopy used to analyze the presence of functional groups (bond types) in organic molecules How IR spectroscopy works:

Structure Determination. How to determine what compound that you have? One way to determine compound is to get an elemental analysis

Química Orgânica I. Ciências Farmacêuticas Bioquímica Química. IR spectroscopy AFB QO I 2007/08 1 AFB QO I 2007/08 2

General Infrared Absorption Ranges of Various Functional Groups

Infrared Spectroscopy: Identification of Unknown Substances

CHEM 3.2 (AS91388) 3 credits. Demonstrate understanding of spectroscopic data in chemistry

Chapter 12 Mass Spectrometry and Infrared Spectroscopy

Table 8.2 Detailed Table of Characteristic Infrared Absorption Frequencies

Learning Guide for Chapter 3 - Infrared Spectroscopy

Vibrational Spectroscopy

12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy

Infrared Spectroscopy. Provides information about the vibraions of functional groups in a molecule

MOLECULAR REPRESENTATIONS AND INFRARED SPECTROSCOPY

ORGANIC - BRUICE 8E CH MASS SPECT AND INFRARED SPECTROSCOPY

Lecture 13 Organic Chemistry 1

2. Infrared spectroscopy

Infrared Spectroscopy: How to use the 5 zone approach to identify functional groups

IR absorption spectroscopy

MASS and INFRA RED SPECTROSCOPY

Advanced Pharmaceutical Analysis

William H. Brown & Christopher S. Foote

Learning Guide for Chapter 3 - Infrared Spectroscopy

Infrared spectroscopy Basic theory

i e l d f Energy (E) = Direction visible ultraviolet X-ray gamma infrared

6. CHARACTERIZATION OF AS (III) IONS BIOSORPTION BY THE LIVE, HEAT AND ALKALINE- TREATED FUNGAL BIOMASS ON THE BASICS OF SURFACE STUDIES

Welcome to Organic Chemistry II

How to Interpret an Infrared (IR) Spectrum

EXPT. 7 CHARACTERISATION OF FUNCTIONAL GROUPS USING IR SPECTROSCOPY

(2) Read each statement carefully and pick the one that is incorrect in its information.

1. Which compound would you expect to have the lowest boiling point? A) NH 2 B) NH 2

Infra-red Spectroscopy

Topic 2.11 ANALYTICAL TECHNIQUES. High Resolution Mass Spectrometry Infra-red Spectroscopy

CHE 325 SPECTROSCOPY (A) CHAP 13A ASSIGN CH 2 CH CH 2 CH CHCH 3

Organic Compound Identification Using Infrared Spectroscopy. Description

CHM 223 Organic Chemistry I Prof. Chad Landrie. Lecture 10: September 20, 2018 Ch. 12: Spectroscopy mass spectrometry infrared spectroscopy

CHEM3331: Fundamentals of Organic Chemistry I Prof. Ognjen Š. Miljanić December 11, 2012

Application of IR Raman Spectroscopy

Homework Assignment #3

E35 SPECTROSCOPIC TECHNIQUES IN ORGANIC CHEMISTRY

CHEM 3760 Orgo I, F14 (Lab #11) (TECH 710)

Abstract. The vibrational properties of pentane, neopentane, polyethylene and polyvinylchloride are

ORGANIC - EGE 5E CH UV AND INFRARED MASS SPECTROMETRY

CHEM 3760 Orgo I, S12, Exp 5 (Lab #6) (TECH 710: IR Unknown)

Objective 4. Determine (characterize) the structure of a compound using IR, NMR, MS.

Spectroscopy. Fourier Transform Infrared (FT-IR) Spectroscopy

Lab 6. Use of VSEPR to Predict Molecular Structure and IR Spectroscopy to Identify an Unknown

Chemistry 343- Spring 2008

Infrared Spectroscopy (IR)

UNIVERSITY OF CALGARY FACULTY OF SCIENCE MIDTERM EXAMINATION CHEMISTRY 353 READ ALL THE INSTRUCTIONS CAREFULLY

Organic Chemistry: CHEM2322

Vibrations. Matti Hotokka

ORGANIC - CLUTCH CH ANALYTICAL TECHNIQUES: IR, NMR, MASS SPECT

Infrared Spectroscopy

7a. Structure Elucidation: IR and 13 C-NMR Spectroscopies (text , , 12.10)

ORGANIC - CLUTCH CH ANALYTICAL TECHNIQUES: IR, NMR, MASS SPECT

Chemistry 3720 Old Exams. Practice Exams & Keys

Types of Molecular Vibrations

1 Which of the following cannot be used to detect alcohol in a breathalyser test? Fractional distillation. Fuel cell. Infrared spectroscopy

February 8, 2018 Chemistry 328N

CH 3. mirror plane. CH c d

Chem HH W11 Notes - Dr. Masato Koreeda Date: January 5, 2011 Topic: _IR Spectroscopy_ page 1 of 3. fingerprint region

Look for absorption bands in decreasing order of importance:

Massachusetts Institute of Technology Organic Chemistry Hour Exam #1. Name. Official Recitation Instructor

Increasing energy. ( 10 4 cm -1 ) ( 10 2 cm -1 )

Infrared Spectral Interpretation

8. Spectrum continued

Organic Spectra Infra Red Spectroscopy H. D. Roth. THEORY and INTERPRETATION of ORGANIC SPECTRA H. D. Roth. Infra Red Spectroscopy

Infrared Spectroscopy

UNIVERSITY OF CALGARY FACULTY OF SCIENCE MIDTERM EXAMINATION CHEMISTRY 353 READ ALL THE INSTRUCTIONS CAREFULLY

ORGANIC - EGE 5E CH. 2 - COVALENT BONDING AND CHEMICAL REACTIVITY

Carbon Compounds. Chemical Bonding Part 2

Spectroscopy. Empirical Formula: Chemical Formula: Index of Hydrogen Deficiency (IHD)

Fourier Transform Infrared Spectroscopy of Metal Ligand Complexes *

CHEM 203. Midterm Exam 1 October 31, 2008 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

Identifying Functional Groups. Why is this necessary? Alkanes. Why is this so important? What is a functional group? 2/1/16

CHEM 203. Final Exam December 15, 2010 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

Chapter 14 Spectroscopy

Spectroscopy in Inorganic Chemistry. Vibration and Rotation Spectroscopy

THEORY OF MOLECULE. A molecule consists of two or more atoms with certain distances between them

Molecular Spectroscopy. H 2 O e -

ORGANIC SPECTROSCOPY NOTES

2. Match the following NMR spectra with one of the following substances. Write you answer in the box along side the spectrum. (16 points) A B C D E F

Determining the Structure of an Organic Compound

Probing Bonding Using Infrared Spectroscopy Chem

Chemistry 2. Assumed knowledge

KOT 222 Organic Chemistry II

2FAMILIES OF CARBON COMPOUNDS:

Transcription:

Infrared Spectroscopy An Instrumental Method for Detecting Functional Groups 1 The Electromagnetic Spectrum Infrared Spectroscopy I. Physics Review Frequency, υ (nu), is the number of wave cycles that pass through a point in one second. It is measured in Hz, where 1 Hz = 1 cycle/sec. Wavelength, λ (lambda), is the length of one complete wave cycle. It is often measured in cm (centimeters). Wavelength and frequency are inversely related: Energy is related to wavelength and frequency by the following formulas: Wavenumbers and energy: υ = c λ E = hυ = hc λ

II. IR Spectroscopy A. Bond Vibrations There are two types of molecular vibrations, stretching and bending. 2 You may have come to think of a molecule as having rigid bond lengths and bond angles, as when you work with your molecular model sets. This is not the actual case, since bond lengths and angles represent the average positions about which atoms vibrate. One way of visualizing bond vibrations is to treat the bond as two balls (atoms) connected by a spring. The stretching frequency of a bond can be approximated by Hooke s Law. In this approximation, two atoms and the connecting bond are treated as a simple harmonic oscillator composed of 2 masses (atoms) joined by a spring:

According to Hooke s law, the frequency of the vibration of the spring is related to the mass and the force constant of the spring, k, by the following formula for the case of a diatomic molecule: 3 _ o υ is the wavenumber (cm -1 ) o k is the force constant o μ is the reduced mass (proportional to the masses of the atoms) Important Relationships in Hooke s Law 1) Masses of Atoms: as the mass of the atoms increases, the frequency of vibration decreases. C-H C-C C-O C-Cl C-Br C-I 3000 cm -1 1200 cm -1 1100 cm -1 750 cm -1 600 cm -1 500 cm -1 2) Force Constant: as the strength of the spring increases, the frequency of the vibration increases. Type of Bond -C-H (sp 3-1s) =C-H (sp 2-1s) C-H (sp - 1s) Approximate Wavenumber Force Constant 5 x 10 5 dyne/cm 2900 cm -1 10 x 10 5 dyne/cm 3100 cm -1 15 x 10 5 dyne/cm 3300 cm -1 B. Other types of Bond Vibrations Vibrational modes are often given descriptive names, such as:

4 C. The Absorption Process The absorption of energy is a quantized process. A molecule absorbs only selected energies (frequencies) of IR radiation. In the absorption process, those frequencies of IR radiation which match the natural vibrational frequencies of the molecule are absorbed in a process called resonance. o The energy absorbed increases the amplitude of the vibrational motions (modes) of the bonds in motion. However, not all bonds in a molecule are capable of absorbing IR radiation, even if the frequency of the IR radiation matches the bond vibrations. Only bonds that possess a dipole moment are capable f absorbing IR radiation. When a polar bond vibrates there is a slight change in the dipole moment of the bond. The changing electrical dipole of the bond can then couple with the incoming electromagnetic field of the IR radiation. D. The IR Spectra The absorption frequencies are specified as wavenumbers in units of reciprocal centimeters (cm-1) The spectrum is a plot of wavenumber [(wavelength) -1 ] on the horizontal axis versus strength of absorption on the vertical axis. The IR is a fingerprint (~500 to 1500 cm -1 ) of the molecule because of the unique and large number of peaks seen for a particular molecule.

5 E. Interpreting IR Spectra 1) Compare your IR to a reference IR if possible. 2) Note the presence and the absence of peaks. 3) Identify Key Peaks Characteristics: The wavenumber where the absorption occurs The peak intensity relative to others in the spectra (stong, medium, weak) The peak shape (spike, broad, very broad) Acetone Ethanol Acetic Acid 4) Consult correlation tables and know the peaks listed below in number 5 5) Know the following four key IR-absorption bands and band properties. a) sp 3 -C-H stretch slightly less than 3000 cm -1 sp 2 =C-H stretch is slightly greater than 3000cm -1 ( k = wave #) sp C-H stretch is much greater than 3000cm -1 ( k = wave #) b) C=C stretch is around 1620 1660 cm -1. Peaks are sharp and of medium intensity c) C=O stretch in the vicinity of 1720 cm -1. Present in aldehydes, ketones, carboxylic acids, esters, amides. Conjugation moves the peak to a lower wavenumber. If present, it is usually the most intensive peak. d) O-H stretch is around 3000 cm -1. Intermolecular H-bonding makes this a very broad peak when the sample is more concentrated In carboxylic acids, this peak is very broad.

6 Bond Type Type of Vibration Frequency (cm 1 ) Intensity C H Alkanes (stretch) 3000 2850 s CH 3 (bend) 1450 and 1375 m CH 2 (bend) 1465 m Alkenes (stretch) 3100 3000 m (out-of-plane bend) 1000 650 s Aromatics (stretch) 3150 3050 s (out-of-plane bend) 900 690 s Alkyne (stretch) 3300 s Aldehyde 2850 and 2750 w C C Alkane Not useful (too many) C=C Alkene 1680 1600 m-w Aromatic 1600 and 1475 m-w CC Alkyne 2250 2100 m-w C=O Aldehyde 1740 1720 s Ketone 1725 1705 s Carboxylic acid 1725 1700 s Ester 1750 1730 s Amide 1680 1630 s Anhydride 1810 and 1760 s Acid chloride 1800 s Carbon dioxide 2400 w C O Alcohols, ethers, esters, carb acids 1300 1000 s O H Alcohols, phenols Free 3650 3600 m H-bonded 3400 3200 (broad) m Carboxylic acid 3400 2400 (broad) m N H Primary and secondary amines, amides (stretch) 3500 3100 m (bend) 1640 1550 m-s C N Amines 1350 1000 m-s C=N Imines and oximes 1690 1640 w-s CN Nitriles 2260 2240 m N=O Nitro 1550 and 1350 s S H Thiols 2550 w C X Fluoride 1400 1000 s Chloride 785 540 s Bromide, iodide <667 s