ORGANIC CHEMISTRY (LL)-PACKAGE
ORGANIC CHEMISTRY (LL)-PACKAGE
8th Edition
ISBN: 9781319316389
Author: VOLLHARDT
Publisher: MAC HIGHER
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Chapter 1, Problem 30P
Interpretation Introduction

Interpretation: The resonance Lewis structure (if possible) for compounds in problem 25 and 28 needs to be represented using the electron-pushing arrows. The major contributor of the resonance hybrid needs to be determined.

Concept Introduction: The compound undergoes resonance, if there is possibility of delocalization of pi electrons. It is possible if there is an alternative double bond with charge or lone pair of the electrons on an atom. In the resonance, movement of electrons takes place from negative to positive charge and this movement is represented by curved arrows.

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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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