
Chemistry: Atoms First
3rd Edition
ISBN: 9781259923142
Author: Burdge
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 6.4, Problem 6.4.1SR
Interpretation Introduction
Interpretation: The formal charges of
Concept Introduction
- A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all
chemical bonds are shared equally among atoms. - This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.
- The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.
- Formal charge of an atom can be determined by the given formula.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Draw the epoxide formed when the following alkene is treated with mCPBA. Click the "draw
structure" button to launch the drawing utility.
draw structure ...
Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic
aromatic substitution.
Explanation
Check
CF3
(Choose one)
OH
(Choose one)
H
(Choose one)
(Choose one)
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy
Identifying electron-donating and electron-withdrawing effects
For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Molecule
Inductive Effects
Resonance Effects
Overall Electron-Density
CF3
O donating
O donating
O electron-rich
O withdrawing
withdrawing
O no inductive effects
O no resonance effects
O electron-deficient
O similar to benzene
OCH3
Explanation
Check
O donating
O donating
○ withdrawing
withdrawing
O no inductive effects
no resonance effects
electron-rich
electron-deficient
O similar to benzene
Х
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center
Chapter 6 Solutions
Chemistry: Atoms First
Ch. 6.2 - Classify the following bonds as nonpolar, polar,...Ch. 6.2 - Classify the following bonds as nonpolar, polar,...Ch. 6.2 - Prob. 1PPBCh. 6.2 - Electrostatic potential maps are shown for HCl and...Ch. 6.2 - Prob. 6.2WECh. 6.2 - Prob. 2PPACh. 6.2 - Prob. 2PPBCh. 6.2 - Prob. 2PPCCh. 6.2 - Prob. 6.3WECh. 6.2 - Prob. 3PPA
Ch. 6.2 - Prob. 3PPBCh. 6.2 - Prob. 6.2.1SRCh. 6.2 - Prob. 6.2.2SRCh. 6.2 - Using data from Table 6.2, calculate the magnitude...Ch. 6.2 - Prob. 6.2.4SRCh. 6.3 - Draw the Lewis structure for carbon disulfide...Ch. 6.3 - Prob. 4PPACh. 6.3 - Prob. 4PPBCh. 6.3 - Prob. 4PPCCh. 6.3 - Prob. 6.3.1SRCh. 6.3 - Prob. 6.3.2SRCh. 6.4 - The widespread use of fertilizers has resulted in...Ch. 6.4 - Prob. 5PPACh. 6.4 - Prob. 5PPBCh. 6.4 - Prob. 5PPCCh. 6.4 - Formaldehyde (CH2O), which can be used 10 preserve...Ch. 6.4 - Prob. 6PPACh. 6.4 - Prob. 6PPBCh. 6.4 - Prob. 6PPCCh. 6.4 - Prob. 6.4.1SRCh. 6.4 - Prob. 6.4.2SRCh. 6.5 - Prob. 6.7WECh. 6.5 - Prob. 7PPACh. 6.5 - Prob. 7PPBCh. 6.5 - Prob. 7PPCCh. 6.5 - How many resonance structures can be drawn for the...Ch. 6.5 - Indicate which of the following are resonance...Ch. 6.6 - Prob. 6.8WECh. 6.6 - Prob. 8PPACh. 6.6 - Prob. 8PPBCh. 6.6 - Prob. 8PPCCh. 6.6 - Prob. 6.9WECh. 6.6 - Prob. 9PPACh. 6.6 - Prob. 9PPBCh. 6.6 - Elements in the same group exhibit similar...Ch. 6.6 - Draw three resonance structures for the hydrogen...Ch. 6.6 - Draw two resonance structures for each speciesone...Ch. 6.6 - Prob. 10PPCCh. 6.6 - Prob. 6.6.1SRCh. 6.6 - Which elements cannot have more than an octet of...Ch. 6.6 - How many electrons are around the central atom in...Ch. 6 - Which of the following atoms must always obey the...Ch. 6 - Prob. 6.2KSPCh. 6 - Prob. 6.3KSPCh. 6 - How many lone pairs are on the central atom in the...Ch. 6 - Prob. 6.1QPCh. 6 - Prob. 6.2QPCh. 6 - Prob. 6.3QPCh. 6 - Prob. 6.4QPCh. 6 - Prob. 6.5QPCh. 6 - Prob. 6.6QPCh. 6 - Prob. 6.7QPCh. 6 - Prob. 6.8QPCh. 6 - For each of the following pairs of elements, state...Ch. 6 - Define electronegativity and explain the...Ch. 6 - Prob. 6.11QPCh. 6 - Prob. 6.12QPCh. 6 - Prob. 6.13QPCh. 6 - Prob. 6.14QPCh. 6 - Prob. 6.15QPCh. 6 - Prob. 6.16QPCh. 6 - Arrange the following bonds in order of increasing...Ch. 6 - Prob. 6.18QPCh. 6 - Prob. 6.19QPCh. 6 - Prob. 6.20QPCh. 6 - Prob. 6.21QPCh. 6 - Prob. 6.22QPCh. 6 - Prob. 6.23QPCh. 6 - Prob. 6.24QPCh. 6 - Prob. 6.25QPCh. 6 - Prob. 6.26QPCh. 6 - Prob. 6.27QPCh. 6 - Prob. 6.28QPCh. 6 - Prob. 6.30QPCh. 6 - Prob. 6.31QPCh. 6 - Prob. 6.32QPCh. 6 - Prob. 6.33QPCh. 6 - Prob. 6.34QPCh. 6 - Draw all of the resonance structures for the...Ch. 6 - Prob. 6.36QPCh. 6 - Prob. 6.37QPCh. 6 - Draw three resonance structures for the molecule...Ch. 6 - Draw three reasonable resonance structures for the...Ch. 6 - Indicate which of the following are resonance...Ch. 6 - Prob. 6.41QPCh. 6 - Prob. 6.42QPCh. 6 - Draw a resonance structure of the guanine molecule...Ch. 6 - Prob. 6.44QPCh. 6 - Give three examples of compounds that do not...Ch. 6 - Prob. 6.46QPCh. 6 - Prob. 6.47QPCh. 6 - Prob. 6.48QPCh. 6 - Prob. 6.49QPCh. 6 - Prob. 6.50QPCh. 6 - Prob. 6.51QPCh. 6 - Prob. 6.52QPCh. 6 - Prob. 6.53QPCh. 6 - Draw Lewis structures for the radical species ClF2...Ch. 6 - Prob. 6.55QPCh. 6 - Prob. 6.56QPCh. 6 - Prob. 6.57QPCh. 6 - Prob. 6.58QPCh. 6 - Prob. 6.59QPCh. 6 - Prob. 6.60QPCh. 6 - Give an example of an ion or molecule containing...Ch. 6 - Prob. 6.62QPCh. 6 - Prob. 6.63QPCh. 6 - Prob. 6.64QPCh. 6 - Are the following statements true or false? (a)...Ch. 6 - Prob. 6.66QPCh. 6 - Prob. 6.67QPCh. 6 - Most organic acids can be represented as RCOOH,...Ch. 6 - Prob. 6.69QPCh. 6 - Prob. 6.70QPCh. 6 - Prob. 6.71QPCh. 6 - The following species have been detected in...Ch. 6 - Prob. 6.73QPCh. 6 - Prob. 6.74QPCh. 6 - The triiodide ion (I3) in which the I atoms are...Ch. 6 - Prob. 6.76QPCh. 6 - Prob. 6.77QPCh. 6 - The chlorine nitrate (ClONO2) molecule is believed...Ch. 6 - Prob. 6.79QPCh. 6 - For each of the following organic molecules draw a...Ch. 6 - Prob. 6.81QPCh. 6 - Draw Lewis structures for the following organic...Ch. 6 - Draw Lewis structures for the following four...Ch. 6 - Prob. 6.84QPCh. 6 - Prob. 6.85QPCh. 6 - Draw three resonance structures for (a) the...Ch. 6 - Prob. 6.87QPCh. 6 - Prob. 6.88QPCh. 6 - Prob. 6.89QPCh. 6 - Draw a Lewis structure for nitrogen pentoxide...Ch. 6 - Prob. 6.91QPCh. 6 - Nitrogen dioxide (NO2) is a stable compound....Ch. 6 - Prob. 6.93QPCh. 6 - Vinyl chloride (C2H3Cl) differs from ethylene...Ch. 6 - Prob. 6.95QPCh. 6 - Prob. 6.96QPCh. 6 - In 1999 an unusual cation containing only nitrogen...Ch. 6 - Prob. 6.98QPCh. 6 - Prob. 6.99QPCh. 6 - Electrostatic potential maps for three compounds...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- The acid-base chemistry of both EDTA and EBT are important to ensuring that the reactions proceed as desired, thus the pH is controlled using a buffer. What percent of the EBT indicator will be in the desired HIn2- state at pH = 10.5. pKa1 = 6.2 and pKa2 = 11.6 of EBTarrow_forwardCUE COLUMN NOTES (A. Determine Stereoisomers it has ⑤ Identify any meso B compounds cl Br cl -c-c-c-c-¿- 1 CI C- | 2,4-Dichloro-3-bromopentanearrow_forwardThe acid-base chemistry of both EDTA and EBT are important to ensuring that the reactions proceed as desired, thus the pH is controlled using a buffer. What percent of the EBT indicator will be in the desired HIn2- state at pH = 10.5. pKa1 = 6.2 and pKa2 = 11.6 of EBTarrow_forward
- What does the phrase 'fit for purpose' mean in relation to analytical chemistry? Please provide examples too.arrow_forwardFor each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects Resonance Effects Overall Electron-Density × NO2 ○ donating O donating O withdrawing O withdrawing O electron-rich electron-deficient no inductive effects O no resonance effects O similar to benzene E [ CI O donating withdrawing O no inductive effects Explanation Check ○ donating withdrawing no resonance effects electron-rich electron-deficient O similar to benzene © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accesarrow_forwardUnderstanding how substituents activate Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation HN NH2 Check X (Choose one) (Choose one) (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Aarrow_forward
- Identifying electron-donating and electron-withdrawing effects on benzene For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Inductive Effects Resonance Effects Overall Electron-Density Molecule CF3 O donating O donating O withdrawing O withdrawing O no inductive effects O no resonance effects electron-rich electron-deficient O similar to benzene CH3 O donating O withdrawing O no inductive effects O donating O withdrawing Ono resonance effects O electron-rich O electron-deficient O similar to benzene Explanation Check Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward* Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forwardDraw TWO general chemical equation to prepare Symmetrical and non-Symmetrical ethers Draw 1 chemical reaction of an etherarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning

Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY