Concept explainers
Interpretation : Whether each molecule or ion in figures 2.2 and 2.3 are legitimate Lewis structures or not should be confirmed.
Concept Introduction : A legitimate Lewis structure is an electron dot and line bond representation in which the total number of valence electrons is indicated. Number of valence electrons around hydrogen is two. Number of valence electrons around carbon, nitrogen, oxygen, fluorine atom is eight. This is called the octet rule.

Answer to Problem 1CTQ
All the given Lewis structures are legitimate.
Explanation of Solution
In
Total number of valence electrons =
Number of electrons consumed for bonds =
Number of remaining electrons =
The remaining four electrons are added to oxygen atom. Then it completes its octet. Therefore, given Lewis structure for water molecule is a legitimate structure.
In
Total number of valence electrons =
Number of electrons consumed for bonds =
Number of remaining electrons =
The remaining twelve electrons are added to two fluorine atom six for each. Then those complete their octet. Therefore, given Lewis structure for
In
Total number of valence electrons =
Number of electrons gained from negative charges =
Total Number of electrons =
Therefore, given Lewis structure for
In
Total number of valence electrons =
Number of electrons consumed for bonds =
Number of remaining electrons =
The remaining two electrons are added to nitrogen atom. Then it completed its octet. Therefore, given Lewis structure for
In
Total number of valence electrons =
Number of electrons consumed for bonds =
Number of remaining electrons =
The remaining six electrons are added to fluorine atom. Then it completed its octet. Therefore, given Lewis structure for
Thus, all the given Lewis structures are legitimate.
Want to see more full solutions like this?
Chapter 2 Solutions
Custom eBook for Organic Chemistry
- Consider the structure of 1-bromo-2-fluoroethane. Part 1 of 2 Draw the Newman projection for the anti conformation of 1-bromo-2-fluoroethane, viewed down the C1-C2 bond. ✡ ぬ Part 2 of 2 H H F Br H H ☑ Draw the Newman projection for the gauche conformation of 1-bromo-2-fluoroethane, viewed down the C1-C2 bond. H F Br H Harrow_forwardPlease help me answer this question. I don't understand how or where the different reagents will attach and it's mostly due to the wedge bond because I haven't seen a problem like this before. Please provide a detailed explanation and a drawing showing how it can happen and what the final product will look like.arrow_forwardWhich of the following compounds is the most acidic in the gas phase? Group of answer choices H2O SiH4 HBr H2Sarrow_forward
- Which of the following is the most acidic transition metal cation? Group of answer choices Fe3+ Sc3+ Mn4+ Zn2+arrow_forwardBased on the thermodynamics of acetic acid dissociation discussed in Lecture 2-5, what can you conclude about the standard enthalpy change (ΔHo) of acid dissociation for HCl? Group of answer choices You cannot arrive at any of the other three conclusions It is a positive value It is more negative than −0.4 kJ/mol It equals −0.4 kJ/molarrow_forwardPLEASE HELP URGENT!arrow_forward
- Draw the skeletal structure corresponding to the following IUPAC name: 7-isopropyl-3-methyldecanearrow_forwardWhich of the following oxyacids is the weakest? Group of answer choices H2SeO3 Si(OH)4 H2SO4 H3PO4arrow_forwardAdd conditions above and below the arrow that turn the reactant below into the product below in a single transformation. + More... If you need to write reagents above and below the arrow that have complex hydrocarbon groups in them, there is a set of standard abbreviations you can use. More... T H,N NC Datarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
