Organic Chemistry
Organic Chemistry
2nd Edition
ISBN: 9781118452288
Author: David R. Klein
Publisher: WILEY
Question
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Chapter 1, Problem 58PP
Interpretation Introduction

Interpretation:

To identify the expected hybridization state and geometry of the nitrogen atoms in Nicotine.

Concept introduction:

The atomic orbitals mix together to form a hybrid orbital which is suitable for forming bonds between the atoms to form a compound.  This mixing of hybrid orbitals is known as hybridization.  The hybridization determines the geometry of the particular atom in the compound.  Shortly to say

sp3hybridized =tetrahedral

trigonal pyramidal(if one lone pair of electron is present)

bent geometry (if two lone pair of electrons are present)

sp2hybridized =trigonal planar

bent geometry (if one lone pair of electrons are present)

sp hybridized =linear

To identify: The hybridization and geometry of the all carbon atoms present in Nicotine.

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Choose the option that is decreasing from biggest to smallest. Group of answer choices: 100 m, 10000 mm, 100 cm, 100000 um, 10000000 nm 10000000 nm, 100000 um, 100 cm, 10000 mm, 100 m 10000000 nm, 100000 um, 10000 mm, 100 cm, 100 m 100 m, 100 cm, 10000 mm, 100000 um, 10000000 nm
Q1. (a) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH3. Use curved arrows to show the electron movement. (b) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH4*. Use curved arrows to show the electron movement.

Chapter 1 Solutions

Organic Chemistry

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