![EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM](https://www.bartleby.com/isbn_cover_images/9781259298424/9781259298424_largeCoverImage.gif)
EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
3rd Edition
ISBN: 9781259298424
Author: SMITH
Publisher: VST
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 4, Problem 4.98CP
Interpretation Introduction
Interpretation:
The Lewis structure of CH3+ and CH3-needs to be drawn and their shapes needs to be predicted.
Concept introduction:
A Lewis structure shows the arrangement of atoms in a molecule such that all the atoms have complete octets. The bonding electrons are represented as lines or bonds between two atoms and non-bonding electrons are represented as dots on the symbol of the respective atoms.
Expert Solution & Answer
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Students have asked these similar questions
Calculate the Enthalpy Change (ΔH) from average bond energies, which have been listed below in KJ/mol, for the following reaction and identify the nature of the reaction:
CH3COOH + CH3OH → CH3COOCH3 + H2O
[C‒H: 413; C‒C: 347; C=O: 745; C=C: 614; Cl‒Cl: 239, C‒O: 358; O‒H: 467]
Although carbon has four bonds in stable molecules, sometimes reactive carbon intermediates that contain carbon atoms without four bonds are formed for very short time periods. Examples of these unstable intermediates include the methyl carbocation (CH 3) + and the methyl carbanion (CH 3) −. Draw Lewis structures for both unstable ions and predict the shape around carbon.
Like several other bonds, carbon-oxygen bonds have lengths and strengths that depend on the bond order. Draw Lewis structures for the following species, and arrange them in order of increasing carbon-oxygen bond strength. (Indicate the order with the numbers from the drop-down list, starting with 1 for the compound with the smallest bond strength to 5 for the compound with the largest bond strength.) H2CO CH4O CO HCO3-(H attached to O) CO32-
Chapter 4 Solutions
EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
Ch. 4.1 - Use electron-dot symbols to show how a hydrogen...Ch. 4.1 - Use electron-dot symbols to show how two chlorine...Ch. 4.1 - How many covalent bonds are predicted for each...Ch. 4.1 - Fill in the lone pairs on each atom to give every...Ch. 4.1 - Prob. 4.5PCh. 4.1 - Draw a Lewis structure for each covalent molecule....Ch. 4.1 - Draw a Lewis structure for dimethyl ether (C2H6O)...Ch. 4.2 - Prob. 4.8PCh. 4.2 - Prob. 4.9PCh. 4.2 - Prob. 4.10P
Ch. 4.3 - Prob. 4.11PCh. 4.3 - Prob. 4.12PCh. 4.4 - Prob. 4.13PCh. 4.4 - Draw resonance structures for each polyatomic...Ch. 4.4 - Nitrous oxide, N2O, is a sweet-smelling gas...Ch. 4.5 - Name each compound: (a) CS2; (b) SO2; (c) PCl5;...Ch. 4.5 - Prob. 4.17PCh. 4.5 - What is the shape around the indicated atom in...Ch. 4.6 - NaNH2, sodium amid, is a salt that contains a...Ch. 4.6 - Prob. 4.20PCh. 4.7 - Using the trends in the periodic table, rank the...Ch. 4.7 - Use electronegativity values to classify the...Ch. 4.7 - Prob. 4.23PCh. 4.8 - Prob. 4.24PCh. 4.9 - Prob. 4.25PCh. 4.9 - Prob. 4.26PCh. 4 - For each pair of compounds, classify the bonding...Ch. 4 - For each pair of compounds, classify the bonding...Ch. 4 - Prob. 4.29PCh. 4 - How many bonds and lone pairs are typically...Ch. 4 - Prob. 4.31PCh. 4 - Fill in the lone pairs needed to give the main...Ch. 4 - Prob. 4.33PCh. 4 - Convert the 3-D model of the general anesthetic...Ch. 4 - Draw a valid Lewis structure for each molecule. Hl...Ch. 4 - Draw a valid Lewis structure for each molecule....Ch. 4 - Prob. 4.37PCh. 4 - Prob. 4.38PCh. 4 - Draw a valid Lewis structure for...Ch. 4 - Draw a valid Lewis structure for phosgene, CCl2O ,...Ch. 4 - Draw a valid Lewis structure for each ion: (a)...Ch. 4 - Draw a valid Lewis structure for each ion: (a)...Ch. 4 - Keeping in mind that some elements violate the...Ch. 4 - Keeping in mind that some elements violate the...Ch. 4 - Prob. 4.45PCh. 4 - Prob. 4.46PCh. 4 - Prob. 4.47PCh. 4 - Prob. 4.48PCh. 4 - Prob. 4.49PCh. 4 - Label each pair of compounds are resonance...Ch. 4 - Prob. 4.51PCh. 4 - Draw three resonance structures for the nitrate...Ch. 4 - Name each covalent compound. PBr3 SO3 NCl3 P2S5Ch. 4 - Name each covalent compound. SF6 CBr4 N2O P4O10Ch. 4 - Prob. 4.55PCh. 4 - Prob. 4.56PCh. 4 - Add lone pairs where needed to give octets and...Ch. 4 - Add lone pairs where needed to give octets and...Ch. 4 - Prob. 4.59PCh. 4 - Match each compound with one of the molecular...Ch. 4 - Prob. 4.61PCh. 4 - Add lone pairs where needed to give octets and...Ch. 4 - Prob. 4.63PCh. 4 - Considering each of the given ball-and stick...Ch. 4 - Prob. 4.65PCh. 4 - Prob. 4.66PCh. 4 - Prob. 4.67PCh. 4 - Predict the bond angles around the indicated atoms...Ch. 4 - Prob. 4.69PCh. 4 - Prob. 4.70PCh. 4 - Rank the atoms in each group in order of...Ch. 4 - Prob. 4.72PCh. 4 - Prob. 4.73PCh. 4 - Using electronegativity values, classify the bond...Ch. 4 - Label the bond formed between carbon and each of...Ch. 4 - Label the bond formed between fluroine and each of...Ch. 4 - Which bond in each pair is more polar-that is, has...Ch. 4 - Which bond in each pair is more polar-that is, has...Ch. 4 - Prob. 4.79PCh. 4 - Prob. 4.80PCh. 4 - Label the polar bonds and then decide if each...Ch. 4 - Label the polar bonds and then decide if each...Ch. 4 - Prob. 4.83PCh. 4 - Explain why H2O is a polar molecule but H2S is...Ch. 4 - Convert each ball-and-stick model to a Lewis...Ch. 4 - Convert each ball-and-stick model to a Lewis...Ch. 4 - Answer the following questions about the molecule...Ch. 4 - Answer the following question about the molecule...Ch. 4 - Prob. 4.89PCh. 4 - Lactic acid gives sour milk its distinctive taste....Ch. 4 - Prob. 4.91PCh. 4 - Prob. 4.92PCh. 4 - Prob. 4.93PCh. 4 - Prob. 4.94PCh. 4 - Isobutyl cyanoacrylate is used in medical glues to...Ch. 4 - Prob. 4.96PCh. 4 - Cyclopropane is a stable compound that contains...Ch. 4 - Prob. 4.98CPCh. 4 - Prob. 4.99CPCh. 4 - Prob. 4.100CP
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
- Formamide, HC(O)NH2, is prepared at high pressures from carbon monoxide and ammonia, and serves as an industrial solvent (the parentheses around the O indicate that it is bonded only to the carbon atom and that the carbon atom is also bonded to the H and the N atoms). Two resonance forms (one with formal charges) can be written for formamide. Write both resonance structures, and predict the bond angles about the carbon and nitrogen atoms for each resonance form. Are they the same? Describe how the experimental determination of the HNH bond angle could be used to indicate which resonance form is more important.arrow_forwardLike several other bonds, carbon-oxygen bonds have lengths and strengths that depend on the bond order. Draw Lewis structures for the following species, and arrange them in order of increasing carbon-oxygen bond strength. HCO3-(H attached to O) CH4O CO32- H2CO COarrow_forwardMany free radicals combine to form molecules that do not contain any unpaired electrons. The driving force for the radical- radical combination reaction is the formation of a new electron-pair bond. Consider the formation of hydrogen peroxide. 2 OH(g) → H₂O₂(g) Write Lewis formulas for the reactant and product species in the chemical equation. Include nonbonding electrons. OH(g) Select Draw Rings More / ||| ||| Erase Q2 Q H₂O₂(g) Select Draw Rings More 3 S H Erase Q2 Q Question Source: McQuarrie, Rock, And Gallogly 4e - General Chemistry Publisher: University Science Barrow_forward
- Methanal can be made through the partial oxidation of methane using O2 in the presence of a catalyst: CH4 (g) + O2 (g) → CH2O(g) + H,O(g) a. Use bond dissociation enthalpies to estimate the enthalpy change for this reaction. Bond ΔΗ (kJ/mol) C-H 413 O=0 498 O=C 745 0-H 463 Enthalpy change = kJ b. Calculate the enthalpy change for this reaction from enthalpies of formation. Substance A;H (kJ/mol) CH4 (g) -74.87 O2 (g) H2 O(g) -241.8 CH20(g) -115.9 Enthalpy change kJarrow_forwardUsing the bond energies provided, calculate the enthalpy of the reaction (∆Hrxn, in kJ) for the combustion of methanol shown below. CH3OH(l) +3/2 O2 (g) → CO2 (g) + 2 H2O(g)arrow_forwardThe carbonate anion, CO32- , is a resonance hybrid. Draw all of the important resonance structures for this molecule. If an atom has a nonzero formal charge, be sure the formal charge is shown clearly in the structure. Use the resonance structures to calculate the average formal charge on each O atom (which are all equivalent in the "true" structure). [Note: all of the important contributing resonance structures have octets around each atom that desires an octet.]arrow_forward
- I need this solution, Calculate the Enthalpy Change (ΔH) from average bond energies, which have been listed below in KJ/mol, for the following reaction and identify the nature of the reaction: CH3COOH + CH3OH → CH3COOCH3 + H2O [C‒H: 413; C‒C: 347; C=O: 745; C=C: 614; Cl‒Cl: 239, C‒O: 358; O‒H: 467arrow_forwardBased on the atom connectivity shown bellow,evaluate the four resonance structure for the thiosulfate ion S2O3 ^2-. Use curved arrows to indicate how you get from one resonance structure to another. Assign formal changes to all atoms and determine which of these resonance structure is the most stable based on a formal charge analysis Explain your answer thoroughly. Look at the picture.arrow_forward2-Butanol can be made by the reaction of 1-butene and water: H2 C=CH-CH,–CH3 (g) + H2O(g) → CH; CH(OH)CH2CH3 (g) a Use bond dissociation enthalpies to estimate the enthalpy change in this reaction. Bond AH (kJ/mol) H-O 463 C=C 610 H-C 413 C-C 346 358 Enthalpy change = kJ b Calculate the enthalpy change for this reaction from enthalpies of formation. Substance AƒH (kJ/mol) CH3 CH(OH)CH2 CH3 (g) -293.1 H2O(g) -241.83 H2C=CH-CH2–CH3 (g) -0.1300 Enthalpy change = kJarrow_forward
- Unshared, or lone, electron pairs play an important role in determining the chemical and physical properties of organic compounds. Thus, it is important to know which atoms carry unshared pairs. Use the structural formulas below to determine the number of unshared pairs at each designated atom. Be sure your answers are consistent with the formal charges on the formulas. The number of unshared pairs at atom a is 4 The number of unshared pairs at atom b is 2 H The number of unshared pairs at atom c is 3 The number of unshared pairs at atom a is The number of unshared pairs at atom b is C-NEN а b H The number of unshared pairs at atom c is Submit Answer Retry Entire Group 8 more group attempts remainingarrow_forwardH 4 H. H:Y:H H The Lewis representation above depicts a reaction between hydrogen (blue) and a main-group element from group (red). | bond(s) In this representation, each Y atom needs with atoms of H. |electron(s) to complete its octet, and gains these electrons by forming unshared electron pair(s) and |bonding electron pair(s) in the product molecule. There are The bonds in the product are|arrow_forwardRank the elements or compounds in the table below in decreasing order of their boiling points. That is, choose 1 next to the substance with the highest boiling point, choose 2 next to the substance with the next highest boiling point, and so on. substance A B C D chemical symbol, chemical formula or Lewis structure H :O: H | || | H-C-C-C-H H | | H Ar | | H H Ag H H | | H-C-C-C-O-H 1 H | H boiling point (Choose one) (Choose one) (Choose one) X (Choose one 1 (highest) 2 3 4 (lowest) 5arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9780534420123/9780534420123_smallCoverImage.gif)
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285199047/9781285199047_smallCoverImage.gif)
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
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