EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 26, Problem 26.30AP
Interpretation Introduction

(a)

Interpretation:

The isomers of the compounds, 2hydroxyfuran and 2hydroxypyrrole are to be drawn. The compound within the set, 2hydroxyfuran or 2hydroxypyrrole, contains the greatest percentage of carbonyl isomer is to be stated with explanation.

Concept introduction:

The tautomerism in which a chemical equilibrium exists between an alcohol also known as enol and a keto form that can be either an aldehyde or ketone is known as keto-enol tautomerism. These forms are also termed as tautomers.

Interpretation Introduction

(b)

Interpretation:

The isomers of the compounds, phenol and 4hydroxypyridine are to be drawn. The compound within the set, phenol or 4hydroxypyridine, contains the greatest percentage of carbonyl isomer is to be stated with explanation.

Concept introduction:

The tautomerism in which a chemical equilibrium exists between an alcohol also known as enol and a keto form that can be either an aldehyde or ketone is known as keto-enol tautomerism. These forms are also termed as tautomers.

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Transmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)
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