ORGANIC CHEMISTRY:PRINCIPLES...(PB)
ORGANIC CHEMISTRY:PRINCIPLES...(PB)
2nd Edition
ISBN: 9780393630770
Author: KARTY
Publisher: NORTON
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Chapter 1, Problem 1.82P
Interpretation Introduction

(a)

Interpretation:

All resonance contributors for the given ion are to be drawn using curved arrows to indicate which pairs of electrons are being shifted.

Concept introduction:

Resonance structure exists in species for which there are two or more valid Lewis structures. Resonance structures are imaginary whereas true species which is shown by the resonance hybrid. Resonance structures have different placement of their valence electrons but not their atoms. Resonance structures with greater number of atoms having a complete octet, more covalent bonds, and fewer atoms having a non-zero formal charge are considered to be stable. Resonance structures are drawn using curved arrows. A curved arrow shows how the electron pair moves. A curved arrow originates from a lone pair of electrons or from a covalent double or triple bond to indicate the specific pair of electrons that are being moved. The arrow points to an atom if the electrons being moved become a lone pair. Otherwise, the arrow points to the center of an existing bond to represent the formation of a new double/triple bond. A resonance structure can be drawn if a lone pair of electrons on an atom is adjacent to multiple bonds, or an incomplete octet on an atom is adjacent to multiple bonds, or there is a ring of alternating single and multiple bonds.

Interpretation Introduction

(b)

Interpretation:

Resonance hybrid for the given anion is to be drawn.

Concept introduction:

For a species, each valid Lewis structure is called a ‘resonance structure’ or a ‘resonance contributor’. A resonance hybrid is a weighted average of all resonance contributors. A partial bond is represented in a resonance hybrid by a dashed line connecting the two atoms. In the resonance hybrid, partial bonds are shown which represent the atoms over which the electrons are being delocalized.

Interpretation Introduction

(c)

Interpretation:

The longest C-C bond for the given ion is to be identified.

Concept introduction:

For a species, each valid Lewis structure is called a ‘resonance structure’ or a ‘resonance contributor’. A resonance hybrid is a weighted average of all resonance contributors. A partial bond is represented in a resonance hybrid by a dashed line connecting the two atoms. In the resonance hybrid, partial bonds are shown which represent the atoms over which the electrons are being delocalized. The atoms involved in the delocalization of electrons gets a partial double bond character and thus have a shorter bond length than C-C single bond.

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The curved arrow notation introduced in Section 1.6B is a powerfulmethod used by organic chemists to show the movement of electronsnot 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 andformed in a reaction. Consider the following three-step process. (a) Addcurved arrows in Step [1] to show the movement of electrons. (b) Use thecurved arrows drawn in Step [2] to identify the structure of X. X isconverted in Step [3] to phenol and HCl.
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.
Draw all resonance contributors for each of the following molecules or ions. Be sure to include the curved arrows that indicate which pairs of electrons are shifted in going from one resonance structure to the next. (a) CH3NO2 (b) CH, CO, (c) CH CHCHCH2 (the ion has two C-C single bonds) (d) C5H5N (a ring is formed by the C and N atoms, and each H is bonded to a C atom) (e) C4H5N (a ring is formed by the C and N atoms, and the N is bonded to one H atom, and each C atom is bonded to one H atom)

Chapter 1 Solutions

ORGANIC CHEMISTRY:PRINCIPLES...(PB)

Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Prob. 1.13PCh. 1 - Prob. 1.14PCh. 1 - Prob. 1.15PCh. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Prob. 1.19PCh. 1 - Prob. 1.20PCh. 1 - Prob. 1.21PCh. 1 - Prob. 1.22PCh. 1 - Prob. 1.23PCh. 1 - Prob. 1.24PCh. 1 - Prob. 1.25PCh. 1 - Prob. 1.26PCh. 1 - Prob. 1.27PCh. 1 - Prob. 1.28PCh. 1 - Prob. 1.29PCh. 1 - Prob. 1.30PCh. 1 - Prob. 1.31PCh. 1 - Prob. 1.32PCh. 1 - Prob. 1.33PCh. 1 - Prob. 1.34PCh. 1 - Prob. 1.35PCh. 1 - Prob. 1.36PCh. 1 - Prob. 1.37PCh. 1 - Prob. 1.38PCh. 1 - Prob. 1.39PCh. 1 - Prob. 1.40PCh. 1 - Prob. 1.41PCh. 1 - Prob. 1.42PCh. 1 - Prob. 1.43PCh. 1 - Prob. 1.44PCh. 1 - Prob. 1.45PCh. 1 - Prob. 1.46PCh. 1 - Prob. 1.47PCh. 1 - Prob. 1.48PCh. 1 - Prob. 1.49PCh. 1 - Prob. 1.50PCh. 1 - Prob. 1.51PCh. 1 - Prob. 1.52PCh. 1 - Prob. 1.53PCh. 1 - Prob. 1.54PCh. 1 - Prob. 1.55PCh. 1 - Prob. 1.56PCh. 1 - Prob. 1.57PCh. 1 - Prob. 1.58PCh. 1 - Prob. 1.59PCh. 1 - Prob. 1.60PCh. 1 - Prob. 1.61PCh. 1 - Prob. 1.62PCh. 1 - Prob. 1.63PCh. 1 - Prob. 1.64PCh. 1 - Prob. 1.65PCh. 1 - Prob. 1.66PCh. 1 - Prob. 1.67PCh. 1 - Prob. 1.68PCh. 1 - Prob. 1.69PCh. 1 - Prob. 1.70PCh. 1 - Prob. 1.71PCh. 1 - Prob. 1.72PCh. 1 - Prob. 1.73PCh. 1 - Prob. 1.74PCh. 1 - Prob. 1.75PCh. 1 - Prob. 1.76PCh. 1 - Prob. 1.77PCh. 1 - Prob. 1.78PCh. 1 - Prob. 1.79PCh. 1 - Prob. 1.80PCh. 1 - Prob. 1.81PCh. 1 - Prob. 1.82PCh. 1 - Prob. 1.1YTCh. 1 - Prob. 1.2YTCh. 1 - Prob. 1.3YTCh. 1 - Prob. 1.4YTCh. 1 - Prob. 1.5YTCh. 1 - Prob. 1.6YTCh. 1 - Prob. 1.7YTCh. 1 - Prob. 1.8YTCh. 1 - Prob. 1.9YTCh. 1 - Prob. 1.10YTCh. 1 - Prob. 1.11YTCh. 1 - Prob. 1.12YTCh. 1 - Prob. 1.13YTCh. 1 - Prob. 1.14YTCh. 1 - Prob. 1.15YTCh. 1 - Prob. 1.16YTCh. 1 - Prob. 1.17YT
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