calculate their degrees of unsaturation, b. circle the bands of interest and draw the corresponding bonds next to the bands, c. and draw a possible structure. a. G3H11N 20 2000 1500 1000 500 2500 WAVENUMBER [cm-1] 4000 3500 3000 001 08 09 TRANSMITTANCE [%]
calculate their degrees of unsaturation, b. circle the bands of interest and draw the corresponding bonds next to the bands, c. and draw a possible structure. a. G3H11N 20 2000 1500 1000 500 2500 WAVENUMBER [cm-1] 4000 3500 3000 001 08 09 TRANSMITTANCE [%]
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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![**Transcription for Educational Website:**
### Instructions
a. Calculate their degrees of unsaturation.
b. Circle the bands of interest and draw the corresponding bonds next to the bands.
c. Draw a possible structure.
### Infrared (IR) Spectrum Analysis
**Chemical Formula:** C₈H₁₁N
**Graph Description:**
- **X-Axis (Wavenumber [cm⁻¹]):**
The graph ranges from 4000 cm⁻¹ to 500 cm⁻¹.
- **Y-Axis (Transmittance [%]):**
The transmittance ranges from 0% to 100%.
**Key Features:**
- The spectrum shows several peaks indicating various bond absorptions.
- There are significant dips in transmittance around the following wavenumbers:
- Near 3300 cm⁻¹, which might indicate the presence of N-H or O-H stretches.
- Around 3000 cm⁻¹, typically associated with C-H stretching.
- Between 1600-1500 cm⁻¹, possibly due to C=C or N-H bending.
- Additional smaller dips appear through 1500-500 cm⁻¹, indicating various fingerprint region absorptions for complex molecular structures.
**Analysis Objective:**
Identify and assign these bands to corresponding molecular vibrations. Use the graph to visualize structural possibilities and molecular interactions given the formula C₈H₁₁N.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1192b206-aad0-45f0-a4e9-87cf04a17bee%2F17104416-6e19-4cdd-a7d6-153e6ee17aa5%2Flaxbl2t_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Transcription for Educational Website:**
### Instructions
a. Calculate their degrees of unsaturation.
b. Circle the bands of interest and draw the corresponding bonds next to the bands.
c. Draw a possible structure.
### Infrared (IR) Spectrum Analysis
**Chemical Formula:** C₈H₁₁N
**Graph Description:**
- **X-Axis (Wavenumber [cm⁻¹]):**
The graph ranges from 4000 cm⁻¹ to 500 cm⁻¹.
- **Y-Axis (Transmittance [%]):**
The transmittance ranges from 0% to 100%.
**Key Features:**
- The spectrum shows several peaks indicating various bond absorptions.
- There are significant dips in transmittance around the following wavenumbers:
- Near 3300 cm⁻¹, which might indicate the presence of N-H or O-H stretches.
- Around 3000 cm⁻¹, typically associated with C-H stretching.
- Between 1600-1500 cm⁻¹, possibly due to C=C or N-H bending.
- Additional smaller dips appear through 1500-500 cm⁻¹, indicating various fingerprint region absorptions for complex molecular structures.
**Analysis Objective:**
Identify and assign these bands to corresponding molecular vibrations. Use the graph to visualize structural possibilities and molecular interactions given the formula C₈H₁₁N.
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