CHEM 242 UV-VIS SPECTROSCOPY, IR SPECTROSCOPY, CHAP 13A ASSIGN AND MASS SPECTROMETRY C 8 H 17 A B C

Similar documents
DEPARTMENT OF CHEMISTRY AND CHEMICAL ORGANIC CHEMISTRY II 202-BZG-05 03

Chapter 12: Mass Spectrometry: molecular weight of the sample

CHM 424L Organic Laboratory, Dr. Laurie S. Starkey Introduction to Mass Spectrometry

Topic 6 Structure Determination Revision Notes

Infrared Spectroscopy

Teacher s Tools Chemistry Organic Chemistry: Nomenclature and Isomerism

e. V Chemistry 262 Winter 2018 Exam 3

Chapter 2 MASS SPECTROMETRY

F322: Alcohols Methylpropan-2-ol ALLOW methylpropan-2-ol [1]

cyclobutane Benzene Ring phenyl

Final Exam, Page 1 of 15. Your full signature

Organic. Carbon Chemistry

IR Spectroscopy Part II

Carbon s unique bonding pattern arises from the hybridization of the electrons.

Carboxylic Acid Derivatives Reading Study Problems Key Concepts and Skills Lecture Topics: Structures and reactivity of carboxylic acid derivatives

Identifying Functional Groups. (Chapter 2 in the Klein text)

Mass Spectrometry Introduction

Organic Chemistry Diversity of Carbon Compounds

Chapter 20: Carboxylic Acids and Nitriles شیمی آلی 2

Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution

Identification of novel endophenaside antibiotics produced by Kitasatospora sp. MBT66

Chapter 18 Carboxylic Acids and Their Derivatives. Nucleophilic Addition- Elimination at the Acyl Carbon

Lecture 10: MS Interpretation Part 4 Postulation of Molecular Structures

Oregon State University

Chemistry 14C Fall 2015 Second Midterm Exam Page 1

Chap 7: Alcohols, Phenols, & Thiols

Equation y = a + b*x Adj. R-Square Value Standard Error Intercept E Slope

Your Name: Question 1. Spectrum Prediction I: Ethyl Acetoacetate. (15 points) ppm ppm ppm ppm. J(A,D) = 8 Hz = 0.

Carboxylic Acids and Esters

Alkenes and Alkynes: Structure and Nomenclature

Chapter 18. Carboxylic Acids and Their Derivatives. Nucleophilic Addition-Elimination at the Acyl Carbon

Trans Fat Determination in the Industrially Processed Edible Oils By Transmission FT-IR Spectroscopy By

Chapter 20: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution

1/3/2011. Chapter 17 Carboxylic Acids and Their Derivatives. Nucleophilic Addition- Elimination at the Acyl Carbon

Chapter 20 Carboxylic Acids. Introduction

R O R' Acid anhydride. Acid halide. Carboxylic acid. Ester O O O O. Nitrile Acyl phosphate Thioester. Amide

Kinetic model of the biomass hydrolysis by polysulfone. membrane with chemically linked acidic ionic liquids via.

PRACTICE PROBLEMS CHEMISTRY

Chapter 19: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution 19.1: Nomenclature of Carboxylic Acid Derivatives (please read)

Ferrocene-based Compartmental Ligand for the Assembly

Name the ester produced when methanol and pentanoic acid react. methyl pentanoate. Name the type of reaction used to make an ester

1 C 2 C 3 C 4 C 5 C 6 C 7 C 8 C

Chemistry 14C Spring 2018 Second Midterm Exam Page 1

The Mass Spectra Analysis for α-ionone and β-ionone

Identification of Aromatic Fatty Acid Ethyl Esters

Chapter 4 - Carbon Compounds

ANSWERS: Isomers. 2) A and F

Please read and sign the Honor Code statement below:

Your Name: Answer Key Question 1. Standard Fragmentations in Mass Spectrometry. (20 points)

13. Carboxylic Acids (text )

unit 9 practice test (organic and biochem)

Chapter 10. Carboxylic Acids and Derivatives. Naming Carboxylic Acids and Derivatives. Carboxylic Acids: RCOOH (RCO 2 H)

Organic Chemistry Laboratory Fall Lecture 3 Gas Chromatography and Mass Spectrometry June

Paper 9: ORGANIC CHEMISTRY-III (Reaction Mechanism-2) Module17: Reduction by Metal hydrides Part-II CHEMISTRY

Carboxylic Acids and Their Derivatives

What is the intermolecular force present in these molecules? A) London B) dipole-dipole C) hydrogen bonding D) ion-dipole E) None. D.

CHAPTER4 ANSWERS. Multiple Choice Questions. Short Answer Questions. 1. (b) 2. (d) 3. (a) 4. (c) 5. (c) 6. (b) 7. (a) 8. (b)

Org/Biochem Final Lec Form, Spring 2012 Page 1 of 6

Chem 60 Takehome Test 2 Student Section

Lecture 20. Herman Emil Fischer Nobel Prize 1902 Sugars, Esters and Purines. April 4, Chemistry 328N

Prelab 6: Carboxylic Acids

Eszopiclone (Lunesta ): An Analytical Profile

This is an addition reaction. (Other types of reaction have been substitution and elimination). Addition reactions are typically exothermic.

Ch 21 Carboxylic Acid Derivatives and Nu Acyl Subst n

CHAPTER-6 IDENTIFICATION, AND CHARACTERISATION OF DEGRADATION IMPURITY IN VALSARTAN TABLETS

Supplement of Evaluation of NO + reagent ion chemistry for online measurements of atmospheric volatile organic compounds

Time (min) Supplementary Figure 1: Gas decomposition products of irradiated DMC.

CHE 102 Exam 3 CH 3 CHCOOH. CH 3 CH 2 CH 2 O d. e. f. CH3 COO g. h. i. O O CH 3 CCH 2 CCH 3

Chemistry 1120 Exam 1 Study Guide

MASS SPECTRA OF HALOGENATED FATTY ACIDS

UNSATURATED HYDROCARBONS

Fundamentals of Organic Chemistry CHEM 109 For Students of Health Colleges Credit hrs.: (2+1)

TEST-7/11 th, 12 th & 12 th Passed /Set-P

Polarization and Circular Dichroism (Notes 17)

Percentage yield of Polysaccharides

Organic Chemistry. Chapter 23. Hill, Petrucci, McCreary & Perry 4 th. Ed. Alkane to Substituent Group methane CH 4 methyl CH 3

INTRODUCTION TO BIOCHEMISTRY/POLYMERS. 3. With respect to amino acids, polypeptides, and proteins, know:

Chapter 12 Alkenes & Alkynes. Organic and BioChem

Chapter 11 Nutrition: Food for Thought

Self-organization of dipyridylcalix[4]pyrrole into a supramolecular cage for dicarboxylates

Cl or C here H 2 N. 4. Consider the following local anesthetic agents and find the pharmacophore. Double bonds. have been omitted for clarity.

Application Note # FTMS-46 solarix XR: Analysis of Complex Mixtures

11/5/ Oxidation of Alkenes: Cleavage to Carbonyl Compounds. Oxidation of Alkenes: Cleavage to Carbonyl Compounds

Alehydes, Ketones and Carboxylic Acid

You must answer FOUR of the SIX questions. Use a SEPARATE answer book for EACH question.

From Atoms to Cells: Fundamental Building Blocks. Models of atoms. A chemical connection

Supporting Information for Manuscript es w. The Effect of Solvent on the Analysis of Secondary Organic Aerosol Using

Functional Derivatives of Carboxylic Acids

DETECTION OF BEESWAX ADULTERATION WITH HYDROCARBONS USING GAS CHROMATOGRAPHY WITH MASS DETECTOR (GC-MS)

B07 Alcohols, Corboxylic Acids & Esters.notebook. November 19, Alcohols

SCH4U Organic Chemistry. hydrocarbon derivatives. mitchell kember

Chapter 11 Nutrition: Food for Thought

6.1 Cis Trans Isomers

Level 3 Chemistry, 2007

Patrick, An Introduction to Medicinal Chemistry 5e Chapter 1 Drugs and drug targets: an overview

Graphene Quantum Dots-Band-Aids Used for Wound Disinfection

KEY NAME (printed very legibly) UT-EID

C. Correct! A compound that consists only of hydrogen and carbon is termed a hydrocarbon.

CHAPTER 3 Amino Acids, Peptides, Proteins

CH [2] (ii) Give the structural formula of another hydrocarbon which is isomeric with the above.

Transcription:

CEM 242 UV-VIS SPECTRSCPY, IR SPECTRSCPY, CAP 13A ASSIGN AND MASS SPECTRMETRY 1. Which choice matches the max of each steroid in the order given? C 8 17 C 8 17 C 8 17 A B C A. 209 nm 241 nm 284 nm B. 241 nm 284 nm 206 nm C. 284 nm 241 nm 206 nm D. 284 nm 206 nm 241 nm 2. Select the most energetically favorable UV transition for 1,3-butadiene. A. n * B. n * C. 2 3* D. * E. 1 4* 3. The IR stretching frequency occurs at the lowest frequency for which of these bonds? A. B B. - C. N- D. S- E. Difficult to predict 4. An oxygen-containing compound shows strong IR absorption at 1630-1780 cm -1 and 3200-3550 cm -1. What type of compound is it likely to be? A. An alcohol B. A carboxylic acid C. An ether D. A ketone E. An aldehyde 5. A split peak for the IR absorption due to bond stretching is observed for the carbonyl group in which of these compounds? A. C 3C 2 C 2 C B. C 3C 2 CCl C. C 3C 2 CN 2 D. C 3C 2 CC 2 C 3 E. C 3C 2 CCC 2 C 3 6. The IR stretching frequency can be predicted to occur at the highest frequency for which of these bonds? A. C B. C F C. C Cl D. C Br E. C I 7. An anticipated IR absorption band may not be observed because: A. it occurs outside the range of the instrument used. B. no change occurs in the dipole moment during the vibration. C. the absorption band is eclipsed by another. D. the intensity is so weak that it cannot be differentiated from instrument noise. E. All of these 1

8. IR evidence for the presence of the C=C would be most difficult to detect in the case of which of these alkenes? A B C D E 9. The IR absorption due to the stretching of which of these carbon-hydrogen bonds occurs at the highest frequency? A. I B. II C. III D. IV E. V I II III IV V 10. The IR spectrum of which type of compound generally exhibits evidence of hydrogen bonding? A. Aldehyde B. Carboxylic acid C. Alkene D. Ester E. Ketone 11. Which of the following molecules most likely generated this IR spectral data? Wavenumber (cm -1 ) 3300 (broad), 3000, 2200, 2100, 1700 Note: This only includes selected peaks. A. B. C. D. E. 12. Which compound would be expected to show intense IR absorption at 2820, 2710 and 1705 cm-1? A. C3CC2C3 B. PhCC3 C. PhC D. C2=CCC3 13. Which compound would be expected to show intense IR absorption at 2250 cm-1? A. C3C2C2C2 B. (C3)2CC2 C. (C3)2CCN D. C3C2C2CN2 14. Which compound would be expected to show intense IR absorption at 1746 cm-1? A. C3C2C2C3 B. C3C2CN C. C3C2C2C3 D. C3C2SC3 2

15. Which compound would be expected to show intense IR absorption at 1680 cm- 16. Ethyne (C C) does not show IR absorption in the region 2000-2500 cm-1 because: A. C stretches occur at lower energies. B. C C stretches occur at about 1640 cm-1. C. there is no change in the dipole moment when the C C bond in ethyne stretches. D. there is a change in the dipole moment when the C C bond in ethyne stretches. 17. Which of the following would not have a C stretch at about 3050 cm-1? A. 1-pentene B. 2-pentene C. 2-methyl-2-pentene D. 2,3-dimethyl-2-pentene E. 2,4-dimethyl-2-pentene 18. Which of the following stretches tends to be the least intense? A. (alcohol) B. (carboxylic acid) C. C D. C= E. C=C 19. Which of the following does not have a broad absorption with one or more spikes that is centered about 3300 cm-1 in the IR? A. (C3C2C2)3N B. (C3C2C2)2N C. C3C2C2N2 D. (C3)3CN2 E. (C2=CC2)2N 20. Which compound would be expected to show intense IR absorption at 3367, 3282 cm-1? A. but-1-ene B. PhC2 C. C3C2C3 D. PhC2N2 21. Which compound would be expected to show intense IR absorption at 1640 cm-1? A. hex-1-ene B. 2-methylheptane C. C3C2C2 D. C3C2CC3 22. The frequency of the stretching vibration of a bond in IR spectroscopy depends on what two quantities? A. the stiffness of the bond and the electronegativity of the atoms B. the electronegativity of the atoms and the nuclear charges of the atoms C. the masses of the atoms and the stiffness of the bond D. the nuclear charges of the atoms and the atomic radii E. the electronegativity of the atoms and the masses of the atoms 23. Which of the following has a C stretch that occurs at the highest stretching frequency? A. hexane B. hex-1-ene C. (E)-hex-2-ene D. hex-1-yne E. hex-2-yne 24. Which compound would show a larger than usual M+2 peak in the mass spectrum? A. C3C2SC3 B. (C3)2CN2 C. C3C2C2 D. C3(C2)2C3 3

25. Which of the following structures is consistent with the IR spectra shown below? A. B. C. D. E. 26. When a high energy electron impacts molecule M in the ionization chamber, what type of species is initially produced? A. cation B. anion C. radical D. radical cation E. radical anion 27. The mass spectrum of alcohols often fail to exhibit detectable M peaks but instead show relatively large peaks. A. M+1 B. M+2 C. M-16 D. M-17 E. M-18 28. The two most abundant isotopes of boron are 10B and 11B, with 11B being about 4 times more abundant. In the mass spectrum of trimethylborate [(C3)3B],. A. the peaks at m/z 103 and m/z 104 have equivalent intensities B. the peak at m/z 103 has an intensity which is 4 times that of the m/z 104 peak C. the peak at m/z 103 has an intensity which is 1/4 the intensity of the peak at m/z 104 D. none of the above 29. What m/z characterizes a strong peak in the mass spectrum of cyclopentanol? A. 86 B. 85 C. 84 D. 70 E. 68 30. Which is the base peak? A. 15 B. 29 C. 44 D. 45 E. 100 Use the following to answer questions 30-31 31. Which is the likely molecular ion (M )? A. 15 B. 29 C. 44 D. 45 E. 100 32. Select the structure of a compound C 6 14 with a base peak at m/z 43. A. C 3C 2C 2C 2C 2C 3 B. (C 3C 2) 2CC 3 C. (C 3) 3CC 2C 3 D. (C 3) 2CC(C 3) 2 E. None of these 4

33. Which of the following structures is consistent with the mass spectrum shown below? A) B) C) D) E) 34. What is the molecular formula of this compound? m/z intensity 84 M 10.00 85 0.56 86 0.04 A. C 5 10 B. C 5 8 C. C 5 24 D. C 6 12 E. C 4 6 2 EXTRA CREDIT 35. Which of the following compounds has the lowest carbonyl stretching frequency? A B C D 36. Which of the following fragment peaks would not be present in the mass spectrum of n-hexane? A. 87 B. 71 C. 57 D. 43 E. 29 37. Predict the base peak for 2-chloro-2-methylpropane A. m/z 15 B. m/z 92 C. m/z 43 D. m/z 57 E. m/z 77 5

NAME DATE ANSWER SEET CEM 242 CAP 13A ASSIGN 1. 13. 25. 37. 2. 14. 26. 38. 3. 15. 27. 39. 4. 16. 28. 40. 5. 17. 29. 41. 6. 18. 30. 42. 7. 19. 31. 43. 8. 20. 32. 44. 9. 21. 33. 45. 10. 22. 34. 46. 11. 23. 35. 47. 12. 24. 36. 48. SP 2014 6