Please only give an answer from the ANSWER CHOICES: Answer Choices (Only PICK ONE) 1-bromobutane 1-cyclopropylethan-1-one 1-ethyl-3-methylbenzene 1,2-dimethoxynenzene 2,3-dimethylbutan-2-ol 3-methylbutan-1-ol 3,3-dimethylbutan-2-one 4-benzylpiperidine 4-methoxybenzaldehyde acetic anhydride acetonitrile acetyl chloride anisole benzaldehyde benzoic acid benzophenone benzyl acetate bromobenzene cyclohex-2-en-1-one cyclohexanone cyclopent-2-en-1-one diethylamine dimethyl malonate ethyl 2-cyanoacetate ethynylbenzene heptanoic acid methyl propionate N-methylaniline N,N-dimethylformamide naphthalene nitrobenzene o-xylene octan-1-amine octan-1-ol p-cresol prop-2-en-1-ol propan-2-one propane-1,3-diol tetrahydrofuran toluene

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Please only give an answer from the ANSWER CHOICES:


Answer Choices (Only PICK ONE)

1-bromobutane
1-cyclopropylethan-1-one
1-ethyl-3-methylbenzene
1,2-dimethoxynenzene
2,3-dimethylbutan-2-ol
3-methylbutan-1-ol
3,3-dimethylbutan-2-one
4-benzylpiperidine
4-methoxybenzaldehyde
acetic anhydride
acetonitrile
acetyl chloride
anisole
benzaldehyde
benzoic acid
benzophenone
benzyl acetate
bromobenzene
cyclohex-2-en-1-one
cyclohexanone
cyclopent-2-en-1-one
diethylamine
dimethyl malonate
ethyl 2-cyanoacetate
ethynylbenzene
heptanoic acid
methyl propionate
N-methylaniline
N,N-dimethylformamide
naphthalene
nitrobenzene
o-xylene
octan-1-amine
octan-1-ol
p-cresol
prop-2-en-1-ol
propan-2-one
propane-1,3-diol
tetrahydrofuran
toluene
**IR Spectra Assignment for Organic Compounds**

The task is to assign the IR spectra given in Questions 1 to 3 to their respective corresponding chemical structures from the list below. Each chemical structure is represented by its skeletal formula, commonly used for representing organic compounds.

**Chemical Structures:**

1. 2-Butene-1-ol (C₄H₈O)
2. Ethylbenzene (C₈H₁₀)
3. Diethylamine (C₄H₁₁N)
4. Phenylacetamide (C₈H₉NO)
5. N,N-Dimethylbenzylamine (C₉H₁₃N)
6. Nitrobenzene (C₆H₅NO₂)
7. N-Methylethanamide (C₃H₇NO)
8. Pentanoic Acid (C₅H₁₀O₂)
9. Acetone (C₃H₆O)
10. Benzene (C₆H₆)
11. 1-Chloropropane (C₃H₇Cl)
12. Benzoic Acid (C₇H₆O₂)
13. Methoxybenzene (C₇H₈O)
14. 1-Octanol (C₈H₁₈O)
15. 1-Bromobutane (C₄H₉Br)
16. Phenyl Ethanoate (C₈H₈O₂)
17. Ethylene Glycol (C₂H₆O₂)
18. Phenylethyne (C₈H₆)
19. Isopropylbenzene (C₉H₁₂)
20. Acetonitrile (C₂H₃N)
21. Cyclohexanone (C₆H₁₀O)
22. 3-Methyl-2-Butanol (C₅H₁₂O)
23. Cyclopentanone (C₅H₈O)
24. 1-Bromo-4-Methylbenzene (C₇H₇Br)
25. Benzamide (C₇H₇NO)
26. Methyl Bezoate (C₈H₈O₂)
27. 1-Chlorocyclopropane (
Transcribed Image Text:**IR Spectra Assignment for Organic Compounds** The task is to assign the IR spectra given in Questions 1 to 3 to their respective corresponding chemical structures from the list below. Each chemical structure is represented by its skeletal formula, commonly used for representing organic compounds. **Chemical Structures:** 1. 2-Butene-1-ol (C₄H₈O) 2. Ethylbenzene (C₈H₁₀) 3. Diethylamine (C₄H₁₁N) 4. Phenylacetamide (C₈H₉NO) 5. N,N-Dimethylbenzylamine (C₉H₁₃N) 6. Nitrobenzene (C₆H₅NO₂) 7. N-Methylethanamide (C₃H₇NO) 8. Pentanoic Acid (C₅H₁₀O₂) 9. Acetone (C₃H₆O) 10. Benzene (C₆H₆) 11. 1-Chloropropane (C₃H₇Cl) 12. Benzoic Acid (C₇H₆O₂) 13. Methoxybenzene (C₇H₈O) 14. 1-Octanol (C₈H₁₈O) 15. 1-Bromobutane (C₄H₉Br) 16. Phenyl Ethanoate (C₈H₈O₂) 17. Ethylene Glycol (C₂H₆O₂) 18. Phenylethyne (C₈H₆) 19. Isopropylbenzene (C₉H₁₂) 20. Acetonitrile (C₂H₃N) 21. Cyclohexanone (C₆H₁₀O) 22. 3-Methyl-2-Butanol (C₅H₁₂O) 23. Cyclopentanone (C₅H₈O) 24. 1-Bromo-4-Methylbenzene (C₇H₇Br) 25. Benzamide (C₇H₇NO) 26. Methyl Bezoate (C₈H₈O₂) 27. 1-Chlorocyclopropane (
This image shows an infrared (IR) spectroscopy graph, which is a common tool used in chemistry for identifying molecular components and their structures. Here is a detailed explanation of the graph:

### Graph Components:

- **X-axis (Horizontal):** Represents the wavenumber (cm⁻¹), which is a measure of frequency used in IR spectroscopy. The range displayed is from 4000 cm⁻¹ to 500 cm⁻¹.
- **Y-axis (Vertical):** Indicates the percentage transmittance (%T), showing how much light passes through the sample. The scale ranges from 0% to 80%.

### Key Peaks and Wavenumbers:

1. **Peak at 2956.14 cm⁻¹**
2. **Peak at 2854.20 cm⁻¹**
3. **Peak at 1743.60 cm⁻¹**
4. **Peak at 1437.56 cm⁻¹**
5. **Peak at 1367.12 cm⁻¹**
6. **Peak at 1263.90 cm⁻¹**

### Interpretation:

- **High Transmittance Regions (70-80%):** These areas represent where most of the light passes through the sample, indicating a lack of absorption due to specific molecular vibrations not being present or intense.

- **Low Transmittance Peaks:** These are the significant parts of the spectrum where specific functional groups within the sample absorb IR radiation. The peaks correspond to different molecular bonds and can provide insights into the molecular structure:
  - **2956.14 cm⁻¹ and 2854.20 cm⁻¹ peaks:** Commonly associated with C-H stretching in alkanes.
  - **1743.60 cm⁻¹ peak:** Typically indicates a carbonyl group (C=O) stretch, common for ketones, esters, or carboxylic acids.
  - **1437.56 cm⁻¹ and 1367.12 cm⁻¹ peaks:** Often associated with bending vibrations of CH2 or CH3 groups.
  - **1263.90 cm⁻¹ peak:** Could indicate C-O stretching, often seen in alcohols, ethers, or esters.

### Conclusion:

This IR spectrum offers valuable information regarding the types of chemical bonds present in the sample, which aids in determining the molecular structure. IR spectroscopy is essential for analyzing organic compounds and is widely used in various fields
Transcribed Image Text:This image shows an infrared (IR) spectroscopy graph, which is a common tool used in chemistry for identifying molecular components and their structures. Here is a detailed explanation of the graph: ### Graph Components: - **X-axis (Horizontal):** Represents the wavenumber (cm⁻¹), which is a measure of frequency used in IR spectroscopy. The range displayed is from 4000 cm⁻¹ to 500 cm⁻¹. - **Y-axis (Vertical):** Indicates the percentage transmittance (%T), showing how much light passes through the sample. The scale ranges from 0% to 80%. ### Key Peaks and Wavenumbers: 1. **Peak at 2956.14 cm⁻¹** 2. **Peak at 2854.20 cm⁻¹** 3. **Peak at 1743.60 cm⁻¹** 4. **Peak at 1437.56 cm⁻¹** 5. **Peak at 1367.12 cm⁻¹** 6. **Peak at 1263.90 cm⁻¹** ### Interpretation: - **High Transmittance Regions (70-80%):** These areas represent where most of the light passes through the sample, indicating a lack of absorption due to specific molecular vibrations not being present or intense. - **Low Transmittance Peaks:** These are the significant parts of the spectrum where specific functional groups within the sample absorb IR radiation. The peaks correspond to different molecular bonds and can provide insights into the molecular structure: - **2956.14 cm⁻¹ and 2854.20 cm⁻¹ peaks:** Commonly associated with C-H stretching in alkanes. - **1743.60 cm⁻¹ peak:** Typically indicates a carbonyl group (C=O) stretch, common for ketones, esters, or carboxylic acids. - **1437.56 cm⁻¹ and 1367.12 cm⁻¹ peaks:** Often associated with bending vibrations of CH2 or CH3 groups. - **1263.90 cm⁻¹ peak:** Could indicate C-O stretching, often seen in alcohols, ethers, or esters. ### Conclusion: This IR spectrum offers valuable information regarding the types of chemical bonds present in the sample, which aids in determining the molecular structure. IR spectroscopy is essential for analyzing organic compounds and is widely used in various fields
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