Organic Chemistry, Ebook And Single-course Homework Access
Organic Chemistry, Ebook And Single-course Homework Access
6th Edition
ISBN: 9781319085841
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 26, Problem 26.12P
Interpretation Introduction

Interpretation:

The aromatic substitution reaction of pyridine-N-oxide takes place at 4 position rather than 3 position is to be explained by giving resonance structure of carbocation intermediate formed.

Concept Introduction:

The aromatic electrophilic substitution reaction takes place at the position which is more resonance stabilized. The resonance structure which has more charge will be less stable. Also more the separation between the charged atoms, more will be the stability of resonance structure. The more stable intermediate will form the product.

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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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