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OCR AS Chemistry

Revision Notes

Home / AS / Chemistry / OCR / Revision Notes / 4. Core Organic Chemistry / 4.7 Analytical Techniques / 4.7.1 Infrared Spectroscopy


4.7.1 Infrared Spectroscopy


Introduction to Infrared Spectroscopy

  • All covalent bonds act rather like springs, as opposed to rigid bars
  • Like springs, the bonds can vibrate in a number of different ways
  • The frequency of vibration occurs in the infra-red region of the electromagnetic spectrum
  • If an organic molecule is irradiated with infra-red energy that matches the natural vibration frequency of its bonds, it absorbs some of that energy and the amplitude of vibration increases
  • This is known as resonance

Different modes of vibration in molecules. Each mode has a characteristic frequency of vibration

Infrared (IR) spectroscopy

  • Infrared (IR) spectroscopy is a technique used to identify compounds based on changes in vibrations of atoms when they absorb IR of certain frequencies
  • A spectrophotometer irradiates the sample with IR radiation and then detects the intensity of IR radiation absorbed by the molecule
  • IR energy is absorbed only if a molecule has a permanent dipole that changes as it vibrates
    • Symmetrical molecules such as O2 or H2, are therefore IR inactive

  • The resonance frequency is the specific frequency at which the bonds will vibrate
  • Rather than displaying frequency, an IR spectrum shows a unit called wavenumber
    • Wavenumber is the reciprocal of the wavelength and has units of cm-1

  • Characteristic absorptions can be matched to specific bonds in molecules
    • This enables chemists to determine the functional groups present

Absorption Range of Bonds

4-6-2-ocr-absorption-range-of-bonds

  • Due to some absorption bands overlapping each other, other analytical techniques such as mass spectroscopy should be used alongside IR spectroscopy to identify an unknown compound

Interpreting & Predicting Infrared Spectra

  • The best way to understand how to interpret an IR spectrum is by looking at examples and becoming familiar with the characteristic features of an IR spectrum

Worked Example

Examine the two spectra shown and determine which one belongs to propan-2-ol and which one belongs to propanoneAnalytical Techniques Question Worked Example - Analysing IR Spectra, downloadable AS & A Level Chemistry revision notes

Answer:

    • IR spectrum A is propanone
      • In IR spectrum A the presence of a strong, sharp absorption around 1710 cm-1 corresponds to the characteristic C=O, carbonyl, group in a ketone.
    • IR spectrum B is propan-2-ol.
      • In spectrum B the presence of a strong, broad absorption around 3200-3600 cm-1 suggests that there is an alcohol group present, which corresponds to the -OH group in propan-2-ol.

Exam Tip

You can be asked to interpret or predict infrared spectra of both familiar and unfamiliar substances

Three of the key peaks to be aware of are:
  1. The narrow scoop caused by the O-H bond of an alcohol at between 3200 and 3600 cm-1 
  2. The sharp spike caused by the carbonyl C=O bond that belongs to many compounds as listed in the data booklet and table above
  3. The broad scoop caused by the O-H bond of a carboxylic acid between 2500 and 3300 cm-1, this right hand side of this peak is often distorted by the peaks from C-H bonds

Uses of Infrared Spectroscopy

  • Infrared spectroscopy is used to identify pollutants in vehicle emissions in the air
    • Sensors detect and measure the amount of pollutants such as carbon monoxide, carbon dioxide and unburnt hydrocarbons
    • This commonly occurs on motorways and in busy town centres to monitor localised pollution

  • Infrared spectroscopy can be used to measure alcohol levels using roadside breathalysers
    • A ray of infrared radiation is passed through the breath that is exhaled into the breathalyser chamber
    • The characteristic bonds of ethanol are detected and measured - the higher the absorbance of infrared radiation, the more ethanol in the person's breath

Fingerprint Region

  • The region below about 1500 cm-1 is called the fingerprint region and is unique to every molecule
  • It has many peaks that can be difficult to assign
  • These peaks represent the complex vibrational interactions that occur between different bonds within a molecule
  • The value of the fingerprint region is in being able to compare the IR spectrum to a known compound from a database and coming up with an exact match
  • This is particularly useful, for example, in identifying a specific member of a homologous series
    • All members of the series will show the same type of bonds present, but no two molecules will have the same fingerprint region

  • Infrared spectroscopy is one of a number of techniques used to determine the structure of organic molecules
    • It is most commonly used in combination with other analytical techniques such as:
      • Elemental analysis - to determine the empirical formula
      • Mass spectrometry - to determine the molecular mass and fragment ions from the whole molecule
      • (NMR spectroscopy is also included in the techniques but this is not covered as part of the AS course)



  • 1. Development of Practical Skills in Chemistry
    • 1.1 Physical Chemistry Practicals
      • 1.1.1 Moles Determination
        • 1.1.2 Acid-Base Titration
          • 1.1.3 Determination of Enthalpy Changes
            • 1.1.4 Reaction - Magnesium & Hydrochloric Acid
            • 1.2 Organic & Inorganic Practicals
              • 1.2.1 Qualitative Analysis of Ions
                • 1.2.2 Synthesis of a Haloalkane
                  • 1.2.3 Preparation of Cyclohexene
                    • 1.2.4 Oxidation of Ethanol
                  • 2. Foundations in Chemistry
                    • 2.1 Atoms & Reactions
                      • 2.1.1 Atomic Structure & Isotopes
                        • 2.1.2 Atomic Structure & Mass Spectrometry
                          • 2.1.3 Compounds, Formulae & Equations
                          • 2.2 Amount of Substance
                            • 2.2.1 Amount of Substance
                              • 2.2.2 Determining Formulae
                                • 2.2.3 Reaction Calculations
                                  • 2.2.4 The Ideal Gas Equation
                                    • 2.2.5 Percentage Yield & Atom Economy
                                    • 2.3 Acid-base & Redox Reactions
                                      • 2.3.1 Acids
                                        • 2.3.2 Acid-base Titrations
                                          • 2.3.3 Redox
                                          • 2.4 Electrons, Bonding & Structure
                                            • 2.4.1 Electron Structure
                                              • 2.4.2 Ionic Bonding & Structure
                                                • 2.4.3 Covalent Bonding & Structure
                                                • 2.5 The Shapes of Simple Molecules & Ions
                                                  • 2.5.1 The Shapes of Simple Molecules & Ions
                                                    • 2.5.2 Electronegativity & Bond Polarity
                                                      • 2.5.3 Intermolecular Forces
                                                    • 3. Periodic Table & Energy
                                                      • 3.1 Periodicity
                                                        • 3.1.1 Periodicity
                                                          • 3.1.2 Ionisation Energy
                                                            • 3.1.3 Structure & Physical Properties
                                                            • 3.2 Group 2
                                                              • 3.2.1 Group 2 Elements
                                                                • 3.2.2 Group 2 Compounds
                                                                • 3.3 The Halogens
                                                                  • 3.3.1 The Halogens
                                                                    • 3.3.2 Uses of Chlorine
                                                                      • 3.3.3 Qualitative Analysis
                                                                      • 3.4 Enthalpy Changes
                                                                        • 3.4.1 Enthalpy Changes
                                                                          • 3.4.2 Calorimetry
                                                                            • 3.4.3 Bond Enthalpies
                                                                              • 3.4.4 Hess' Law
                                                                              • 3.5 Reaction Rates
                                                                                • 3.5.1 Simple Collision Theory
                                                                                  • 3.5.2 Catalysis
                                                                                    • 3.5.3 The Boltzmann Distribution
                                                                                    • 3.6 Chemical Equilibrium
                                                                                      • 3.6.1 Dynamic Equilibrium
                                                                                        • 3.6.2 Le Chatelier’s Principle
                                                                                          • 3.6.3 The Equilibrium Constant, Kc
                                                                                        • 4. Core Organic Chemistry
                                                                                          • 4.1 Basic Concepts
                                                                                            • 4.1.1 Chemical Names & Formulae
                                                                                              • 4.1.2 Functional Groups
                                                                                                • 4.1.3 Structural Isomerism
                                                                                                  • 4.1.4 Reaction Mechanisms
                                                                                                  • 4.2 Alkanes
                                                                                                    • 4.2.1 Introduction to Alkanes
                                                                                                      • 4.2.2 Reactions of Alkanes
                                                                                                        • 4.2.3 Free Radical Substitution of Alkanes
                                                                                                        • 4.3 Alkenes
                                                                                                          • 4.3.1 Introduction to Alkenes
                                                                                                            • 4.3.2 Stereoisomerism in Alkenes
                                                                                                              • 4.3.3 Addition Reactions of Alkenes
                                                                                                                • 4.3.4 Electrophilic Addition
                                                                                                                  • 4.3.5 Polymers from Alkenes
                                                                                                                  • 4.4 Alcohols
                                                                                                                    • 4.4.1 Properties of Alcohols
                                                                                                                      • 4.4.2 Reactions of Alcohols
                                                                                                                      • 4.5 Haloalkanes
                                                                                                                        • 4.5.1 Reactions of Haloalkanes
                                                                                                                          • 4.5.2 Nucleophilic Substitution of Haloalkanes
                                                                                                                            • 4.5.3 Hydrolysis of Primary Haloalkanes
                                                                                                                              • 4.5.4 Environmental Concerns of Organohalogen Use
                                                                                                                              • 4.6 Organic Synthesis
                                                                                                                                • 4.6.1 Techniques
                                                                                                                                  • 4.6.2 Synthetic Routes
                                                                                                                                  • 4.7 Analytical Techniques
                                                                                                                                    • 4.7.1 Infrared Spectroscopy
                                                                                                                                      • 4.7.2 Mass Spectrometry
                                                                                                                                        • 4.7.3 Combined Techniques


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                                                                                                                                      Author: Richard

                                                                                                                                      Richard has taught Chemistry for over 15 years as well as working as a science tutor, examiner, content creator and author. He wasn’t the greatest at exams and only discovered how to revise in his final year at university. That knowledge made him want to help students learn how to revise, challenge them to think about what they actually know and hopefully succeed; so here he is, happily, at SME.


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