ORGANIC CHEMISTRY-ETEXT REG ACCESS
ORGANIC CHEMISTRY-ETEXT REG ACCESS
12th Edition
ISBN: 9781119308362
Author: Solomons
Publisher: WILEY
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Chapter 14, Problem 28P
Interpretation Introduction

Interpretation:

The aromaticity of cyclononatetraenyl anion and the dianion formed by [16] annulene is to be explained.

Concept introduction:

In accordance with the Huckel’s rule, aromatic compounds contain a planar ring and have a conjugated pi system with (4n+2)π electrons, where n=0,1,2,3,...

Aromatic compounds contain conjugated pi bonds.

All the atoms in the aromatic ring have an unhybridized p orbital.

Compounds that are planar, cyclic and having conjugated pi system, with (4n)π electrons are antiaromatic. They are highly unstable.

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Relative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 20 NaоH 0103 Br (B) H2504 → (c) (A) 100- MS-NU-0547 80 40 20 31 10 20 100- MS2016-05353CM 80 60 100 MS-NJ-09-3 80 60 40 20 45 J.L 80 S1 84 M+ absent राग 135 137 S2 62 164 166 11 S3 25 50 75 100 125 150 175 m/z
Don't used hand raiting and don't used Ai solution
Don't used hand raiting

Chapter 14 Solutions

ORGANIC CHEMISTRY-ETEXT REG ACCESS

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