The reason of same molecular structure which show minimum formal charge and also obey octet rule of given compounds in each case needs to be explained. Concept Introduction: Lewis dot structure is the representation which shows the bonding between atoms present in a molecule. It shows lone pairs and bond pairs that existing on each bonded atom. Lewis dot structure is also known as Lewis dot formula or electron dot structure. Formal charge on each atom can be determined with the help of number of valence shell electrons, number of lone pair electrons and bond pair electrons. The formula for the formal charge can be written as: FC = VE – LE – bond pair FC = formal charge VE = Valence electrons LE = number of lone pair electrons Bond pair = Number of bond pairs

Question

Want to see the full answer?

Answer 1

Question

Chapter 13, Problem 123AE

Interpretation Introduction

Interpretation: The reason of same molecular structure which show minimum formal charge and also obey octet rule of given compounds in each case needs to be explained.

Concept Introduction:

Lewis dot structure is the representation which shows the bonding between atoms present in a molecule. It shows lone pairs and bond pairs that existing on each bonded atom. Lewis dot structure is also known as Lewis dot formula or electron dot structure.

Formal charge on each atom can be determined with the help of number of valence shell electrons, number of lone pair electrons and bond pair electrons. The formula for the formal charge can be written as:

FC = VE – LE – bond pairFC= formal chargeVE = Valence electrons LE= number of lone pair electrons Bond pair = Number of bond pairs

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.)