ORG.CHEM.WILEYPLUSNEXTGEN.W/LLTEXT+STDY.
ORG.CHEM.WILEYPLUSNEXTGEN.W/LLTEXT+STDY.
4th Edition
ISBN: 9781119832638
Author: Klein
Publisher: WILEY
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Chapter 17, Problem 55IP
Interpretation Introduction

Interpretation: For the given cycloheptatrienone and cyclopentadienone, the more partial negative character on the oxygen atom of cycloheptatrienone should be explained.

Concept introduction:

  • A five membered ring will be aromatic if it contains six π electrons. In order to have six π electrons, one of the carbon atoms must possess two electrons. It should be a carbanion.
  • A seven membered ring will be aromatic if it contains six π electrons. In order to have six π electrons in a seven membered ring one of the carbon atom must possess an empty p orbital. This carbocation exhibits a continuous system of overlapping and p orbitals and has six π electrons.
  • Aromatic compounds are more stable than non-aromatic compound
  • Cycloheptatrienone reveals resonance structures with aromatic character
  • Cyclopentadienone reveals resonance structures with  anti-aromatic character

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Five isomeric alkenes. A through each undergo catalytic hydrogenation to give 2-methylpentane The IR spectra of these five alkenes have the key absorptions (in cm Compound Compound A –912. (§), 994 (5), 1643 (%), 3077 (1) Compound B 833 (3), 1667 (W), 3050 (weak shoulder on C-Habsorption) Compound C Compound D) –714 (5), 1665 (w), 3010 (m) 885 (3), 1650 (m), 3086 (m) 967 (5), no aharption 1600 to 1700, 3040 (m) Compound K Match each compound to the data presented. Compound A Compound B Compound C Compound D Compound
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