INFRARED SPECTROSCOPY 2

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Texas A&M University *

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237

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Chemistry

Date

Oct 30, 2023

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17

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e A T T T e —— |/ | I INFRARED SPECTROSCOPY Name JUH]1ENNe Penarloy pate (0Q [ 25/23 TA. K ate Monheim Room Color WORKSHEET Open the IR Tutor program. Initially, a screen will open telling you to change your monitor resolu- tion. DO NOT change the screen resolution, just hit continue! Once you have opened the IR Tutor program, use the program to answer the following questions. Each question can be answered with the information found in the program. 1. Whereis the IR region relative to visible light? @ near the red b. near the violet 2. How did Hershel first detect IR light? pointing a prism 3. Isall infrared light the same wavelength? N O 4. What does A stand for? wavelength 5. What does v stand for? Lrequency 6. What does v(bar) stand for? wavenumpey 7. Write an equation that relates energy (E) to wavelength. E=hc/M 8. From your equation, what happens to energy as the wavelength increases? eheraq M i€y decredse 9. Write an equation that relates energy and wavenumbers. 10. From this new equation, what happens to wavenumbers as energy increases? incregie 97 NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY . T
% WRITE-UP 11. What range of wavenumbers represents the mid IR region? 4000~ ypocm™! 12. Why are lenses not used in IR instruments? Lenses absorb lignt 13. Which type of IR instrument measures all wavelengths of IR at once? 2. Classical @)mn‘er Transform 14. What happens to the potential energy of a spring if it is stretched from its equilibrium length? incregyes 15. What happens to the potential energy of a spring if it is compressed from its equilibrium length? . increase p 16. What happens to the frequency of a vibration if you increase the force constant? ncrease 17. What happens to the frequency of a vibration if you increase the mass? decreayge 18. The vibrations of molecular bonds are not as simple as a symmetric parabolic graph. What is happening to the bond in a molecule as the energy levels out? (This is on the right side of the graph.) bond prea ks 19. What is the change in energy associated with an overtone? TYansitions ope [,u0 10 nigher 20. What must happen to the dipole for a specific vibration to show up in IR Spectroscopy? it must cha f’)q e 21. What are the three stretches that a water molecule has? pen SYManedlic mmetric NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
Bend N B9 pectrum in 23. Which takes more energy, a bend or a stretch? (Look at where they are on the s wavenumbers, and then look at your equation from question 9.) chetch 24. Draw the four molecular vibrations for CO, using arrows to show the direction of the stretch or bend. Label which one(s) will result in IR absorption. —_— 25. What is the range in wavenumbers of the fingerprint region? (Remember that we need a high and a low, not just “anything below...”) <400 NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
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[T me gufisum‘meqrw pend Ik r\mu,vjm.e_‘f{'.\filaflsh# NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
DATA & ANALYSIS Infrared Spectroscopy =Ml | AL apnswne anhiumatlic _Cifi'r?etuvl\ bendSo | [l | [ wlg‘f i | anti symmetyic | N/ étrgfcv' 02+ 11114 | | | | L~ CHz antigymm- = A me)r'c/vl\l CH ben 00 e —wor 000, Z500). 20001800, 1600 .F 1001200 541000 B0 €00 em 4 26. Notice that 1-heptyne has a peak at 3300 cm™), but it is not there in 4-octyne. Why is it not there in 4-octyne? The triple—bond ptacemen f NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
.| WRITE-UP did this t 4_0nyfle' Why d . , and 10! ¢ 0 m-'isalsoonb’"‘l'heptyne (MD”'“’“LF 27. NoticethatdlepeakatZlO c ; mmefl'ldlll peak disappear? 1+ WA 4 ) bt NI [scigsoring | e d ] os | 02—+ a0 Tm T S S 1400 ' | Toluene i 4“ +—— yomatic : o2~ eireteh ] %% ;n f'::zj mm"ad 28. How can we see the difference between sp? and sp® C-H stretches when looking at an IR? sp3 has 4 smaller pPeak steeper spT s NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
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L F Al : M uoUg\fa £ T-¢ et ¥ | . oo 140 120 10007 |80 600 em! 400 | summetyic | 10 GIE“ | [ | s \ 1 | | | | E | 2000 1800 1600 1400 1200 1000 800 600 ¢! 400 00 Ym ww . ww B NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
SR T nsqmmi streron | 024—— D I ahmmmmnmlmvam carbonyl peak will be for each of these compounds. 29. List the wavenumbers where the 1721 1702 1A b 30, What happens to the position of the carbonyl peak as resonance of the carbonyl increases? decreases NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
¥ DATA & ANALYSIS Infrared Spectroscopy 00 | Eeewa ||| | | 4000 300 3000 2%0 | 2000 1S00 1600 1400 1200 {000 BOO 600 om! 400 31. List the wavenumbers where the carbonyl peak will be for each of these compounds. L 44 d4d 1906 1naz IEE (110 (Lad 32. What is causing the change in where the carbonyl peak is for the different rings? The blflq&V ‘rhe}( nnqgs qet | aew NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
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WRITE-UP § - retch | 08 T | stretch oaif- T i (AN KN PRy REE | SRR YT IR / ;ogm,,“ oc("(,j [ 1600 1400 ' {200 - 1000 eco €00 em™1 400 33. How could you tell the difference between an ethyl acetate and diethyl ether if you used only IR spectroscopy? (Hint: What peak would ethyl acetate have that diethyl ether would not?) ¢=0 Stretch peak In the diethyl efhey NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
00 B | ! 40 30 00 200 200 180 1600 1400 1200 1000 800 600 en 400 NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
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- Ly 1000 - o4 eool i & = R . . . : ® = - - L WRvENUEER! 41 NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
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an T 000 won Y 10 ) anam NOT FOR DISTRIBUTION - FOR INSTRUCTORS USE ONLY
organic Monday, September 25, 2023 7:12 PM Analyst Date PerkinElmer Spectrum IR Version 107 2 Monday, September 25, 2023 7.12 PM LN ': 2928.79cn|;‘-1 N Allcane § 50 4 0 carveny = 3 17p4.92cm-1 26+ , ; . ; , ; - 4000 3500 3000 2500 2000 1500 1000 450 cm-1 organic 1043 Heptanol- Jullienne Penaflor Page 1

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