Lewis structures of all the important resonance forms of NO 2 + is to be determined. Concept introduction: The steps to draw the Lewis structure of the molecule are as follows: Step 1: Find the central atom and place the other atoms around it. The atom in a compound which has the lowest group number or lowest electronegativity considered as the central atom. Step 2: Calculate the total number of valence electrons. Step 3: Connect the other atoms around the central atoms to the central atom with a single bond and lower the value of valence electrons by 2 of every single bond. Step 4: Allocate the remaining electrons in pairs so that the octet of each atom is satisfied. Step 5: Convert the lone pair into a bond pair if required. When bonds in a molecule can be expressed by different Lewis structures then resonance structures are used to depict the bonding in that molecule. These resonance structures have the same placement of atoms but different locations of bonding and lone pairs of electrons also one resonance form can be converted into another by moving lone pairs to bonding positions, and vice versa.

Question

Want to see the full answer?

Answer 1

Question

Chapter 10, Problem 10.9P

(a)

Interpretation Introduction

Interpretation:

Lewis structures of all the important resonance forms of NO2+ is to be determined.

Concept introduction:

The steps to draw the Lewis structure of the molecule are as follows:

Step 1: Find the central atom and place the other atoms around it. The atom in a compound which has the lowest group number or lowest electronegativity considered as the central atom.

Step 2: Calculate the total number of valence electrons.

Step 3: Connect the other atoms around the central atoms to the central atom with a single bond and lower the value of valence electrons by 2 of every single bond.

Step 4: Allocate the remaining electrons in pairs so that the octet of each atom is satisfied.

Step 5: Convert the lone pair into a bond pair if required.

When bonds in a molecule can be expressed by different Lewis structures then resonance structures are used to depict the bonding in that molecule. These resonance structures have the same placement of atoms but different locations of bonding and lone pairs of electrons also one resonance form can be converted into another by moving lone pairs to bonding positions, and vice versa.

(b)

Interpretation Introduction

Interpretation:

Lewis structures of all the important resonance forms of NO2F is to be determined.

Concept introduction:

To draw the Lewis structure of the molecule there are following steps:

Step 1: Find the central atom and place the other atoms around it. The atom in a compound which has the lowest group number or lowest electronegativity considered as the central atom.

Step 2: Calculate the total number of valence electrons.

Step 3: Connect the other atoms around the central atoms to the central atom with a single bond and lower the value of valence electrons by 2 of every single bond.

Step 4: Allocate the remaining electrons in pairs so that each atom can get 8 electrons.

When bonds in a molecule can be expressed by different Lewis structures then resonance structures are used to depict the bonding in that molecule. These resonance structures have the same placement of atoms but different locations of bonding and lone pairs of electrons also one resonance form can be converted into another by moving lone pairs to bonding positions, and vice versa.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Using the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.

Synthesis of Dibenzalacetone [References] Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. Question 1 1 pt Question 2 1 pt Question 3 1 pt H Question 4 1 pt Question 5 1 pt Question 6 1 pt Question 7 1pt Question 8 1 pt Progress: 7/8 items Que Feb 24 at You do not have to consider stereochemistry. . Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple reactants using the + sign from the drop-down menu. ? 4

Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)