Student Solutions Manual to Accompany General Chemistry
Student Solutions Manual to Accompany General Chemistry
4th Edition
ISBN: 9781891389733
Author: McQuarrie, Donald A., Carole H.
Publisher: University Science Books
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Chapter 9, Problem 9.1P
Interpretation Introduction

Interpretation:

The Be2 molecule does not exist under normal conditions.  This has to be explained on the basis of MOT theory.

Concept Introduction:

Molecular orbital theory:

Molecular orbital theory suggests the grouping of all atomic orbitals having comparable energy and proper symmetry.

Postulates of MOT is,

  • Atomic orbitals of same energy and proper symmetry combine together to form molecular orbitals.
  • The movement of electrons in a molecular orbital is influenced by all the nuclei of combining atoms.
  • The number of molecular orbitals formed is equal to the number of combining atomic orbital when two atomic orbitals combine two molecular orbitals are formed.  One molecular orbital has high energy than the corresponding atomic orbitals and is called antibonding orbital and the other one with lower energy is called bonding orbital.
  • In molecular orbitals, the electrons are filled according to the Pauli’s exclusion principle, Aufbau principle and the Hund’s rule.

Bond order=(Nb)-(Na)2

Where, Nb is number of electrons in bonding orbital.

Na is number of electrons in antibonding orbital.

Expert Solution & Answer
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Explanation of Solution

The atomic number of Be is four.

The electronic configuration of Be=1s22s2

The molecular electronic configuration of Be2 molecule=(σ1s)2(σ*1s)2(σ2s)2(σ*2s)2

MO diagram of Be2 is,

Student Solutions Manual to Accompany General Chemistry, Chapter 9, Problem 9.1P

  Figure 1

The bond order can be calculated as,

  Bond order =(Nb)-(Na)2

There are four electrons in bonding and antibonding orbitals.

  Bond order=(4)-(4)2                  =0

The zero bond order refers that the molecule does not exist.

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PLEASE READ!!! I DONT WANT EXAMPLES, I DONT WANT WORDS OR PARAGRAPHS FOR THE MECHANISM!!! THANKS First image: QUESTION 6. I have to show, with ARROWS and STRUCTURES, the mechanism of the reaction at the bottom. Also I have to show by mecanism why the reaction wouldn't work if the alcohol was primary. I also tried to draw the mechanism, tell me what to change. Please note that its an AMIDE thats formed not an AMINE the nitrogen has ONE hydrogen and one Phenyl-C-Phenyl. I already asked for this mechanism and got as a final product ...-NH2 not whats shown on the picture, thank you Ths second part. QUESTION 3. I just need a way to synthesize the lactone A, I already started please continue from where I left it  Second image: I simply need the products, substrates or reagents, thank you
Indicate how to prepare a 10% sodium hydroxide (NaOH) solution to a slightly alkaline pH.

Chapter 9 Solutions

Student Solutions Manual to Accompany General Chemistry

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