Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Question

Please what molecule is this

The image consists of two graphs which provide spectroscopic data for "Molecule 5." ### Top Graph: Infrared (IR) Spectrum - **Y-axis:** % Transmittance - **X-axis:** Wavenumber (cm⁻¹), ranging from 4000 to 500 #### Key Features: - **Alkyl Halide Absorption:** Noted around the 3000 cm⁻¹ mark, indicating the presence of C-H (sp³) bonds. - **Significant Peaks:** Two peaks are labeled as C-81Br and C-79Br, appearing close to 500 cm⁻¹, indicative of C-Br bond stretching. ### Bottom Graph: Nuclear Magnetic Resonance (NMR) Spectrum - **Y-axis:** No specific label, generally represents intensity. - **X-axis:** Chemical shift (δ, ppm), ranging from 5.0 to 0.0 #### Peak Characteristics: 1. **1 (sextet):** Appears around 3.8 ppm, likely representing a split peak due to coupling with adjacent protons. 2. **2 (quintet):** At approximately 1.7 ppm, showing a quintet pattern. 3. **3 (doublet and triplet):** - *Doublet:* Around 1.4 ppm, typically suggesting two neighboring equivalent hydrogens. - *Triplet:* Near 1.0 ppm, indicating three neighboring equivalent hydrogens. These spectra are typically used to identify functional groups and structural components within the molecule, aiding in molecular characterization and analysis.
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Transcribed Image Text:The image consists of two graphs which provide spectroscopic data for "Molecule 5." ### Top Graph: Infrared (IR) Spectrum - **Y-axis:** % Transmittance - **X-axis:** Wavenumber (cm⁻¹), ranging from 4000 to 500 #### Key Features: - **Alkyl Halide Absorption:** Noted around the 3000 cm⁻¹ mark, indicating the presence of C-H (sp³) bonds. - **Significant Peaks:** Two peaks are labeled as C-81Br and C-79Br, appearing close to 500 cm⁻¹, indicative of C-Br bond stretching. ### Bottom Graph: Nuclear Magnetic Resonance (NMR) Spectrum - **Y-axis:** No specific label, generally represents intensity. - **X-axis:** Chemical shift (δ, ppm), ranging from 5.0 to 0.0 #### Peak Characteristics: 1. **1 (sextet):** Appears around 3.8 ppm, likely representing a split peak due to coupling with adjacent protons. 2. **2 (quintet):** At approximately 1.7 ppm, showing a quintet pattern. 3. **3 (doublet and triplet):** - *Doublet:* Around 1.4 ppm, typically suggesting two neighboring equivalent hydrogens. - *Triplet:* Near 1.0 ppm, indicating three neighboring equivalent hydrogens. These spectra are typically used to identify functional groups and structural components within the molecule, aiding in molecular characterization and analysis.
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