EBK ORGANIC CHEMISTRY-PRINT COMPANION (
EBK ORGANIC CHEMISTRY-PRINT COMPANION (
4th Edition
ISBN: 9781119776741
Author: Klein
Publisher: WILEY CONS
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Chapter 1.10, Problem 20CC
Interpretation Introduction

Interpretation: The reason for free rotation of sigma bonds in contrast to no rotation in pi bonds at room temperature needs to be explained.

Concept Introduction: σ and π bonds are type of covalent bonds that are formed by the overlapping of the atomic orbitals. The difference between two is that head-to-head overlapping of atomic orbitals results in σ bond formation whereas lateral overlapping of atomic orbitals results in π bond formation.

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6) Explain how o and a bonds are similar and how they are different. A) Differences: o bonds are stronger and result from end- to -end overlap and all single bonds are o bonds; a bonds between the same two atoms are weaker because they result from side-by-side overlap, and multiple bonds contain one or more bonds (in addition to a o bond). B) Similarities: Both types of bonds result from overlap of atomic orbitals on adjacent atoms. C) Both A and B are correct
6) Explain how o and a bonds are similar and how they are different. A) Differences: o bonds are stronger and result from end-to-end overlap and all single bonds are o bonds; a bonds between the same two atoms are weaker because they result from side-by-side overlap, and multiple bonds contain one or more n bonds (in addition to a o bond). B) Similarities: Both types of bonds result from overlap of atomic orbitals on adjacent atoms. C) Both A and B are correct 7) How many o and a bonds are present in the molecule HCN (H-C=N) ? A) two o (H-C and C-N) and two A B) two o (H-C and C-N) and one C) one o (H-C) and three n
Nitrogen is capable of forming single, double, or triple bonds, and the figure that follows shows the potential energy as a function of internuclear distance for each of these types of bonds. Match the three curves in the figure (A, B and C) to the three types of bonds. Explain your reasoning.
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