OWLv2 with LabSkills for Gilbert/Martin's Experimental Organic Chemistry: A Miniscale & Microscale Approach, 6th Edition, [Instant Access], 4 terms (24 months)
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Chapter 8.3, Problem 9E

(a)

Interpretation Introduction

Interpretation:

The structure of compound C10H14 based on spectrum obtained from H NMR needs to be drawn.

Concept Introduction :

By using hydrogen NMR, it is possible to determine how many hydrogens in each molecule which gives only the relative number of hydrogens and not the absolute. The peaks obtained from the H-NMR indicates that either there is one hydrogen or more than 2 hydrogens based on the size of the peak but it cannot determine how many hydrogens. For which the ratio is to eb compared to determine the absolute hydrogen.

(b)

Interpretation Introduction

Interpretation:

The structure of compound C3H8O based on spectrum obtained from H NMR needs to be drawn.

Concept Introduction :

By using hydrogen NMR, it is possible to determine how many hydrogens in each molecule which gives only the relative number of hydrogens and not the absolute. The peaks obtained from the H-NMR indicates that either there is one hydrogen or more than 2 hydrogens based on the size of the peak but it cannot determine how many hydrogens. For which the ratio is to eb compared to determine the absolute hydrogen.

(c)

Interpretation Introduction

Interpretation:

The structure of compound C8H9Cl based on spectrum obtained from H NMR is as follows:

Concept Introduction :

By using hydrogen NMR, it is possible to determine how many hydrogens in each molecule which gives only the relative number of hydrogens and not the absolute. The peaks obtained from the H-NMR indicates that either there is one hydrogen or more than 2 hydrogens based on the size of the peak but it cannot determine how many hydrogens. For which the ratio is to eb compared to determine the absolute hydrogen.

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