Organic Chemistry: Structure and Function
Organic Chemistry: Structure and Function
8th Edition
ISBN: 9781319079451
Author: K. Peter C. Vollhardt, Neil E. Schore
Publisher: W. H. Freeman
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Chapter 2, Problem 37P
Interpretation Introduction

Interpretation: All polarized covalent bonds present in functional groups examples in table 2-3 with partial positive and negative charge should be identified and labeled.

  Organic Chemistry: Structure and Function, Chapter 2, Problem 37P , additional homework tip  1

Concept introduction: A functional group is defined as an atom or group of certain atoms that confer reactivity to the overall organic compound. They undergo specific reactions. Majority of functional groups are polarized in nature. The presence of functional groups controls the reactivity of organic moiety as a whole.

The major functional groups are given as follows:

  Organic Chemistry: Structure and Function, Chapter 2, Problem 37P , additional homework tip  2

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The curved arrow notation introduced in Section 1.6B is a powerful method used by organic chemists to show the movement of electrons not only in resonance structures, but also in chemical reactions.Because each curved arrow shows the movement of two electrons, following the curved arrows illustrates what bonds are broken and formed in a reaction. Consider the following three-step process. (a) Add curved arrows in Step [1] to show the movement of electrons. (b) Use the curved arrows drawn in Step [2] to identify the structure of X. X is converted in Step [3] to phenol and HCl.
The curved arrow notation introduced in Section 1.6 is a powerful method used by organic chemists to show the movement of electrons not only in resonance structures, but also in chemical reactions. Since each curved arrow shows the movement of two electrons, following the curved arrows illustrates what bonds are broken and formed in a reaction. Consider the following three-step process. (a) Add curved arrows in Step [1] to show the movement of electrons. (b) Use the curved arrows drawn in Step [2] to identify the structure of X. X is converted in Step [3] to phenol and HCl.
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