Chemistry & Chemical Reactivity, Hybrid Edition (with OWLv2 24-Months Printed Access Card)
9th Edition
ISBN: 9781285462530
Author: John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher: Cengage Learning
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Chapter 8, Problem 66GQ
Draw resonance structures for the SO2 molecule, and determine the formal charges on the S and O atoms. Are the S—O bonds polar, and is the molecule as a whole polar? If so, what is the direction of the net dipole in SO2? Is your prediction confirmed by the electrostatic potential surface? Explain briefly.
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Chapter 8 Solutions
Chemistry & Chemical Reactivity, Hybrid Edition (with OWLv2 24-Months Printed Access Card)
Ch. 8.2 - Draw Lewis electron dot structures for CH3Cl...Ch. 8.2 - Prob. 2CYUCh. 8.2 - Prob. 3CYUCh. 8.2 - Prob. 4CYUCh. 8.2 - Prob. 1RCCh. 8.2 - 2. Which one of the species in the list below is...Ch. 8.2 - Prob. 3RCCh. 8.2 - Prob. 4RCCh. 8.3 - Prob. 1CYUCh. 8.3 - 1. What is the formal charge of the P atom in the...
Ch. 8.4 - Draw resonance structures for the bicarbonate ion,...Ch. 8.4 - 1. For which of the following species, SO32−, NO+,...Ch. 8.4 - Prob. 2RCCh. 8.5 - Sketch the Lewis structures for CIF2+ and CIF2....Ch. 8.5 - Prob. 1QCh. 8.5 - Prob. 2QCh. 8.5 - Prob. 1RCCh. 8.5 - Prob. 2RCCh. 8.6 - What is the shape of the dichloromethane (CH2C12)...Ch. 8.6 - Give the electron-pair geometry and molecular...Ch. 8.6 - Draw the Lewis structure for lCl2, and then decide...Ch. 8.6 - Prob. 4CYUCh. 8.6 - Which of the following species has...Ch. 8.6 - Prob. 2RCCh. 8.6 - What is the approximate ClCCl bond angle in...Ch. 8.6 - 4. What is the molecular geometry of N2O (where...Ch. 8.7 - Draw the resonance structures for SCN. What are...Ch. 8.7 - For each of the following molecules, decide...Ch. 8.7 - Prob. 1RCCh. 8.7 - 2. Which of the following best describes the...Ch. 8.7 - Three resonance forms can be drawn for the...Ch. 8.8 - The electrostatic potential surface for SOCl2 is...Ch. 8.8 - Using the bond dissociation enthalpies in Table...Ch. 8.8 - Prob. 1RCCh. 8.8 - Prob. 2RCCh. 8.9 - 1. Which of the following species has the longest...Ch. 8.9 - 2. Which of the following species has the largest...Ch. 8.9 - 3. Use bond dissociation enthalpies to estimate...Ch. 8 - Give the periodic group number and number of...Ch. 8 - Give the periodic group number and number of...Ch. 8 - For elements in Groups 4A-7A of the periodic...Ch. 8 - Prob. 4PSCh. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Show all possible resonance structures for each of...Ch. 8 - Show all possible resonance structures for each of...Ch. 8 - Prob. 11PSCh. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Determine the formal charge on each atom in the...Ch. 8 - Determine the formal charge on each atom in the...Ch. 8 - Determine the formal charge on each atom in the...Ch. 8 - Determine the formal charge on each atom in the...Ch. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Prob. 18PSCh. 8 - Prob. 19PSCh. 8 - The following molecules or ions all have three...Ch. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Draw a Lewis structure for each of the following...Ch. 8 - Give approximate values for the indicated bond...Ch. 8 - Give approximate values for the indicated bond...Ch. 8 - Phenylalanine is one of the natural amino acids...Ch. 8 - Acetylacetone has the structure shown here....Ch. 8 - For each pair of bonds, indicate the more polar...Ch. 8 - For each of the bonds listed below, tell which...Ch. 8 - Urea, (NH2)2CO, is used in plastics and...Ch. 8 - Considering both formal charges and bond...Ch. 8 - Considering both formal charge and bond...Ch. 8 - Three resonance structures are possible for...Ch. 8 - Three resonance structures are possible for the...Ch. 8 - Compare the electron dot structures of the...Ch. 8 - Compare the electron dot structures of the...Ch. 8 - The chemistry of the nitrite ion and HNO2: (a) Two...Ch. 8 - Draw the resonance structures for the formate ion,...Ch. 8 - Prob. 39PSCh. 8 - Consider the following molecules: (a) CH4 (b)...Ch. 8 - Which of the following molecules is(are) polar?...Ch. 8 - Prob. 42PSCh. 8 - Give the bond order for each bond in the following...Ch. 8 - Prob. 44PSCh. 8 - In each pair of bonds, predict which is shorter....Ch. 8 - In each pair of bonds, predict which is shorter....Ch. 8 - Prob. 47PSCh. 8 - Compare the carbon-oxygen bond lengths in the...Ch. 8 - Consider the carbon-oxygen bond in formaldehyde...Ch. 8 - Compare the nitrogen-nitrogen bond in hydrazine,...Ch. 8 - Ethanol can be made by the reaction of ethylene...Ch. 8 - Methanol can be made by partial oxidation of...Ch. 8 - Hydrogenation reactions, which involve the...Ch. 8 - Phosgene, Cl2CO, is a highly toxic gas that was...Ch. 8 - The compound oxygen difluoride is quite reactive,...Ch. 8 - Oxygen atoms can combine with ozone to form...Ch. 8 - Prob. 57GQCh. 8 - Prob. 58GQCh. 8 - Which of the following compounds or ions do not...Ch. 8 - Prob. 60GQCh. 8 - Draw resonance structures for the formate ion,...Ch. 8 - Prob. 62GQCh. 8 - Prob. 63GQCh. 8 - What is the principle of electroneutrality? Use...Ch. 8 - Prob. 65GQCh. 8 - Draw resonance structures for the SO2 molecule,...Ch. 8 - What are the orders of the NO bonds in NO2 and...Ch. 8 - Which has the greater ONO bond angle, NO2 or NO2+?...Ch. 8 - Compare the FClF angles in CIF2+ and ClF2. Using...Ch. 8 - Draw an electron dot structure for the cyanide...Ch. 8 - Draw the electron dot structure for the sulfite...Ch. 8 - Dinitrogen monoxide, N2O, can decompose to...Ch. 8 - The equation for the combustion of gaseous...Ch. 8 - The cyanate ion, OCN, has the least...Ch. 8 - Vanillin is the flavoring agent in vanilla extract...Ch. 8 - Explain why (a) XeF2 has a linear molecular...Ch. 8 - The formula for nitryl chloride is ClNO2 (in which...Ch. 8 - Hydroxyproline is a less-common amino acid. (a)...Ch. 8 - Amides are an important class of organic...Ch. 8 - Prob. 81GQCh. 8 - The molecule shown here. 2-furylmelhanethiol, is...Ch. 8 - Dihydroxyacetone is a component of quick-tanning...Ch. 8 - It is possible to draw three resonance structures...Ch. 8 - Acrolein is used to make plastics. Suppose this...Ch. 8 - Molecules in space: (a) In addition to molecules...Ch. 8 - 1,2-Dichloroethylene can be synthesized by adding...Ch. 8 - The molecule pictured below is epinephrine, a...Ch. 8 - You are doing an experiment in the laboratory and...Ch. 8 - Prob. 90ILCh. 8 - A paper published in the research Journal Science...Ch. 8 - Uracil is one of the bases in RNA, a close...Ch. 8 - Prob. 93SCQCh. 8 - Prob. 94SCQCh. 8 - Bromine-containing species play a role in...Ch. 8 - Acrylamide, H2C=CHCONH2, is a known neurotoxin and...
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- Best Lewis Formula and Molecular Geometry A student writes the Lewis electron-dot formula for the carbonate anion, CO32, as a Does this Lewis formula obey the octet rule? Explain. What are the formal charges on the atoms? Try describing the bonding for this formula in valence bond terms. Do you have any difficulty doing this? b Does this Lewis formula give a reasonable description of the electron structure, or is there a better one? If there is a better Lewis formula, write it down and explain why it is better. c The same student writes the following resonance description for CO2: Is there something wrong with this description? (What would you predict as the geometries of these formulas?) d Is one or the other formula a better description? Could a value for the dipole moment help you decide? e Can you write a Lewis formula that gives an even better description of CO2? Explain your answer.arrow_forwardDraw all the equivalent resonance structures for BrO 3¯ on a piece of paper and then fill in the blanks. Draw the structure in such a way that the formal charge on the central atom is zero. Molecular geometry: Number of equivalent resonance structures: Bond order of Br-O bond(s): (fractions rounded to 2 decimal places, e.g. 1/2 will be 0.50 , 4/3 will be 1.33 and 5/3 will be 1.67) Formal charge on terminal atoms participating in resonancearrow_forwardConsider the SO 3 molecule. How many valence electrons does the molecule have? How many lone pairs of electrons are on the central atom? How many lone pairs of electrons in total are on the substituent atoms? How many resonance structures can be drawn for the molecule? If the ion doesn't exhibit resonance, indicate "1" as only one structure can be drawn for the molecule.arrow_forward
- Nitrogen is capable of forming single, double, or triple bonds, and the figure that follows shows the potential energy as a function of internuclear distance for each of these types of bonds. Match the three curves in the figure (A, B and C) to the three types of bonds. Explain your reasoning.arrow_forwardA compound composed of sulfur and fluorine has an empirical formula of SF. The structure of this compound has a formal charge of zero on all elements in the compound. Draw the Lewis structure for this substance. (Assign lone pairs and radical electrons where appropriate.)arrow_forwardChoose the best Lewis structure for OCN. (It will help to work out the missing formal charges for the atoms in these different structures) [Image description: Lewis structure A has a C atom singly bound to a O atom and a N atom. There are three electron pairs on O and three electron pairs on N. Lewis structure B has a C atom singly bound to a O atom and triply bound to a N atom. There are three electron pairs on O and one electron pair on N. Lewis structure C has a C atom triply bound to a O atom and singly bound to a N atom. There is one electron pair on O and three electron pairs on N. Lewis structure D has a C atom doubly bound to a O atom and a N atom. There are two electron pairs on O and two electron pairs on N.] :0-c-N: :0-c=N: :0=C-N: o=c=N: A B Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a b В C C d Darrow_forward
- 13) The average C−C bond dissociation energy (D) is 350 kJ/mol and the average C=C bond dissociation energy is 728 kJ/mol. Based on these values, which is stronger: a σ or a π bond?arrow_forwardCarbon, nitrogen, and oxygen form two different polyatomic ions: cyanate ion (NCO) and fulminate ion (CNO). Write Lewis structures for each anion, including near-equivalent resonance structures (do not add any arrows between structures) and indicating formal charges. The isocyanate ion also has two near-equivalent structures, but the formal charge on the nitrogen attom cannot be reduced to zero: Cyanate ion (NCO)arrow_forwardConsider the following ion: BrO3¯. a) Show the full electron configuration for Br. b) Draw the most correct Lewis structure for BrO3¯ and briefly explain why your Lewis structure is correct. c) If the structure is stabilised by resonance, draw at least one of the possible resonance forms. If it is not stabilised by resonance, briefly explain why. d) What is the electronic geometry of BrO3-? What is its molecular shape? e) Does BrO3 have a dipole moment? Briefly justify your answer. f) On average, would you expect IO3¯ to have longer or shorter bonds than BrO3¯? Briefly explain your answer. g) Which of the following molecules would you expect to have the lowest vapour pressure? Briefly explain your choice. Br HO HO. Br- Compound A Compound B Compound C h) What is the molecular formula for Compound C? What is the empirical formula for Compound C?arrow_forward
- a) Below is a lewis structure of CSO. Draw two resonance structures of this molecule. Assign any formal charges if necessary. b) Now look at your structures. Do they represent equivalent or nonequivalent resonance structures of the original? Why or why not? c) Of all three structures, which contributes the most to the overall resonance hybrid and why? Rank the other two in terms of their contributionarrow_forwardPart A) Draw the following lewis structures and give the formal charges for the atoms as well as the number of valence electrons I2 Part B)According to VSEPR theory, why are bonds and lone pairs spaced as far apart as possible? Part C)Why can we ignore the disposition of the lone pairs on terminal atoms? Part D)What are the bond angles for a molecule having an octahedral electronic geometry with two lone pairs and four bonds on the central atom?arrow_forwardWhy does the molecule NO2+ have the arrangement ONO+rather than NOO+? For each arrangement draw all possiblevalid Lewis and resonance structures (there should be six total,three for each arrangement, each of which has complete octetson all atoms) and include formal charges. Explain your results.arrow_forward
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