Assign the hydrogens from C4H10O to this spectra. ### Analysis of Spectroscopy Data#### Infrared (IR) Spectroscopy Graph- **X-axis**: Wavenumber (cm⁻¹)- **Y-axis**: % TransmittanceThe IR spectrum shows several peaks ranging from 4000 to 500 cm⁻¹. Key features include a broad peak around 3400 cm⁻¹, indicating an O-H bond, typical for alcohols or phenols. Other notable peaks indicate various bond stretches and bends.#### Proton Nuclear Magnetic Resonance (NMR) Spectroscopy Graph- **X-axis**: Chemical Shift (PPM)- **Y-axis**: Relative IntensityThe NMR spectrum contains the following signals:- **4 PPM**: Broad singlet indicating 1 hydrogen atom (marked as 'd').- **3 PPM**: Doublet indicating 2 hydrogen atoms (marked as 'c').- **1.5 PPM**: Nonet indicating 1 hydrogen atom (marked as 'b').- **1 PPM**: Doublet indicating 6 hydrogen atoms (marked as 'a').Each signal reflects different environments of hydrogen atoms in the molecule. The signal splitting patterns (singlet, doublet, nonet) provide insights into the number of adjacent hydrogens.

DBE is double bond equivalent. This DBE formula gives us a idea about number of double bond or…

Answered: % Transmittance 4 100- 50- 0- 4000 OH…

% Transmittance 4 100- 50- 0- 4000 OH 3000 broad singlet, 1H ,(d) T- doublet, 2H (c) 3 2000 1500 Wavenumber (cm-¹) nonet, 1H (b) 2 PPM man 1000 1 500 doublet, 6H (a) 0

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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Spectroanalytical Methods

Spectroanalytical methods measure the wavelength and intensity of radiations that are either emitted or absorbed by a molecular or atomic species. These methods are useful for evaluating the electronic or atomic arrangement of the molecules of a given analyte.

Question

Assign the hydrogens from C4H10O to this spectra.

### Analysis of Spectroscopy Data

#### Infrared (IR) Spectroscopy Graph

- **X-axis**: Wavenumber (cm⁻¹)
- **Y-axis**: % Transmittance

The IR spectrum shows several peaks ranging from 4000 to 500 cm⁻¹. Key features include a broad peak around 3400 cm⁻¹, indicating an O-H bond, typical for alcohols or phenols. Other notable peaks indicate various bond stretches and bends.

#### Proton Nuclear Magnetic Resonance (NMR) Spectroscopy Graph

- **X-axis**: Chemical Shift (PPM)
- **Y-axis**: Relative Intensity

The NMR spectrum contains the following signals:

- **4 PPM**: Broad singlet indicating 1 hydrogen atom (marked as 'd').
- **3 PPM**: Doublet indicating 2 hydrogen atoms (marked as 'c').
- **1.5 PPM**: Nonet indicating 1 hydrogen atom (marked as 'b').
- **1 PPM**: Doublet indicating 6 hydrogen atoms (marked as 'a').

Each signal reflects different environments of hydrogen atoms in the molecule. The signal splitting patterns (singlet, doublet, nonet) provide insights into the number of adjacent hydrogens.

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