8 HR201403000NS 18) The partial chemical structure and ¹H NMR spectrum of a compound with the formula C4H10O. Determine which of the following structures fit the spectrum (A-D). Provide a brief rationalization of the structure. 4H B) Peak 1: Peak 2: () HE 3.47 ppm 1.21 ppm 6H Triplet D) XOH 1 0 Quartet ppm A) 4 Identity of Unknown: Explanation: ASTOR SERVICES FOR CHILDREN & FAMILIES www.
8 HR201403000NS 18) The partial chemical structure and ¹H NMR spectrum of a compound with the formula C4H10O. Determine which of the following structures fit the spectrum (A-D). Provide a brief rationalization of the structure. 4H B) Peak 1: Peak 2: () HE 3.47 ppm 1.21 ppm 6H Triplet D) XOH 1 0 Quartet ppm A) 4 Identity of Unknown: Explanation: ASTOR SERVICES FOR CHILDREN & FAMILIES www.
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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
B) 
C) 
D) 
**Identity of Unknown:**
__________
**Explanation:**
__________
(Note: The images of the structures (A–D) are simple line drawings representing different molecular structures. A thorough explanation should include which structure fits the given NMR data based on the chemical shifts, integration, and splitting patterns.)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ffe9fe32c-b492-41de-b627-5e5dec5bc081%2F99891f2e-1898-4298-9038-6b842555e83e%2Fq9b3gnb_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Question:**
18) The partial chemical structure and \( ^1H \) NMR spectrum of a compound with the formula \( C_4H_{10}O \). Determine which of the following structures fit the spectrum (A – D). Provide a brief rationalization of the structure.
**NMR Spectrum Analysis:**
The NMR spectrum shown includes two peaks:
- **Peak 1:**
- Chemical shift: 3.47 ppm
- Integration: 4H
- Splitting pattern: Quartet
- **Peak 2:**
- Chemical shift: 1.21 ppm
- Integration: 6H
- Splitting pattern: Triplet
The x-axis is labeled from 0 to 9 ppm, representing the chemical shift in parts per million (ppm).
**Structural Options:**
A) 
B) 
C) 
D) 
**Identity of Unknown:**
__________
**Explanation:**
__________
(Note: The images of the structures (A–D) are simple line drawings representing different molecular structures. A thorough explanation should include which structure fits the given NMR data based on the chemical shifts, integration, and splitting patterns.)
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