LCPO CHEMISTRY W/MODIFIED MASTERING
8th Edition
ISBN: 9780135214756
Author: Robinson
Publisher: PEARSON
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Textbook Question
Chapter 7, Problem 7.24A
Three resonance structures for anisole (Problem 7.20) are shown. Calculate formal charges on C and O atoms and decide which structure makes the largest contribution to the resonance hybrid.
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The two compounds nitrogen dioxide and dinitrogentetraoxide are introduced in Section 3.13.(a) NO2 is an odd-electron compound. Draw the bestLewis diagrams possible for it, recognizing that oneatom cannot achieve an octet configuration. Use formal charges to decide whether that should be the(central) nitrogen atom or one of the oxygen atoms.(b) Draw resonance forms for N2O4 that obey the octetrule. The two N atoms are bonded in this molecule.
Carbon, 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)
C, N, and O are from groups 4, 5, and 6, and their atomic numbers are 6, 7, and 8.
(1) Give a reasonable Lewis structure for CN2−, including formal charges (N.B. the C is the central atom). 2
(2) Give a reasonable Lewis structure for CO2−, including formal charges (N.B. the C is the central atom). 3
(3) Give a reasonable Lewis structure for O2−, including formal charges. 2
(4) Give a reasonable Lewis structure for O3, including formal charges (N.B. the molecule is not cyclic) (5) What is the oxydation state of C in OCN− (N.B. C is the central atom)?
Chapter 7 Solutions
LCPO CHEMISTRY W/MODIFIED MASTERING
Ch. 7 - Use the electro negativity values in Figure 7.4...Ch. 7 - Conceptual APPLY 7.2 An electrostatic potential...Ch. 7 - The dipole moment of AgCI in the gas phaseis...Ch. 7 - Predict which bond has greater percent ionic...Ch. 7 - Select the correct electron-dot structure for H2S...Ch. 7 - Use the octet rule to predict the molecular...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Select the correct electron-dot structure for...Ch. 7 - Identify the correct electron-dot structure(s) for...
Ch. 7 - Prob. 7.11PCh. 7 - Which oxygen species do you predict to be most...Ch. 7 - Draw an electron-dot structure for the following...Ch. 7 - There are two molecules with the formula C2H6O...Ch. 7 - The following structure is a representation of...Ch. 7 - Draw two possible electron-dot structures for the...Ch. 7 - Called “laughing gas, nitrous oxide (N2O) is...Ch. 7 - Draw as many resonance structures as possible for...Ch. 7 - Prob. 7.19PCh. 7 - Prob. 7.20ACh. 7 - Calculate the formal charge on each atom in the...Ch. 7 - Start with the electron-dot structure for the...Ch. 7 - Calculate formal charges on the C and O atoms in...Ch. 7 - Three resonance structures for anisole (Problem...Ch. 7 - The toxicity of the organophosphate insecticides...Ch. 7 - Prob. 7.26PCh. 7 - Prob. 7.27PCh. 7 - The following structure is a representation of the...Ch. 7 - The electron-dot structure for the nerve a gentsar...Ch. 7 - Draw the new electron-dot structures indicated by...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - Two electrostatic potential maps are shown, one of...Ch. 7 - Prob. 7.34CPCh. 7 - Which of the following drawings is most likely to...Ch. 7 - The following ball-and-stick molecular model is a...Ch. 7 - The following hall-and-stick molecular model is a...Ch. 7 - Sinapaldehyde, a compound present in the toasted...Ch. 7 - Vitamin C (ascorbic acid) has the following...Ch. 7 - Match the following descriptions with the type of...Ch. 7 - Why do two atoms come together to form a covalent...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Predict which of the following bonds should be...Ch. 7 - Prob. 7.45SPCh. 7 - What general trends in electro negativity occur in...Ch. 7 - Predict the electro negativity of the undiscovered...Ch. 7 - Order the following elements according to...Ch. 7 - Order the following elements according to...Ch. 7 - Which of the following substances contain bonds...Ch. 7 - Use the electro negativity data in Figure 7.4 to...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Which of the substances...Ch. 7 - Which of the substances...Ch. 7 - Order the following compounds according to the...Ch. 7 - Order the following compounds according to the...Ch. 7 - Prob. 7.58SPCh. 7 - Using only the elements Ca, Cl, and Si, give...Ch. 7 - The dipole moment of BrCl is 0.518 D, and the...Ch. 7 - Prob. 7.61SPCh. 7 - Prob. 7.62SPCh. 7 - Prob. 7.63SPCh. 7 - Why does the octet rule apply primarily to...Ch. 7 - Which of the following substances contains an atom...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron.dot structure for the hydronium...Ch. 7 - Oxalic acid, H2C2O4 , is a mildly poisonous...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Prob. 7.72SPCh. 7 - Identify the fourth-row elements, X, that form the...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Prob. 7.79SPCh. 7 - Methylphenidate (C14H19NO2) , marketed as Ritalin,...Ch. 7 - Pregabalin (C8H17NO2) , marketed as Lyric a, is an...Ch. 7 - The following molecular model is that of...Ch. 7 - Ibuprofen C 13 H 18 O 2 marketed under such brand...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can for...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Benzene has the following structural formula. Use...Ch. 7 - Draw three resonance structures for sulfur...Ch. 7 - Some mothballs used when storing clothes are made...Ch. 7 - Four different structures (a), (b), (c), and (d)...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Calculate formal charges for the C and O atoms in...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Prob. 7.102SPCh. 7 - Prob. 7.103SPCh. 7 - Boron trifluoride reacts with dimethyl ether to...Ch. 7 - Thiofulminic acid, HCNS, has recently been...Ch. 7 - Draw two rcsonancc strutur for methyl isocyanate,...Ch. 7 - In the cyanatc ion. 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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
- Consider the pyrosulfate ion, S2O72-. It has no sulfur–sulfur nor oxygen–oxygen bonds. (a) Write a Lewis structure for the pyrosulfate ion using only single bonds. (b) What is the formal charge on the sulfur atoms for the Lewis structure you drew in part (a)? (c) Write another Lewis structure using six bonds and two O—S bonds. (d) What is the formal charge on each atom for the structure you drew in part (c)?arrow_forwardThree known isomers exist of N2CO, with the atoms in these sequences: NOCN; ONNC; and ONCN. Write resonance structures for each isomer and use formal charge to predict which isomer is the most stable.arrow_forwardAssign formal charges to all atoms in the following Lewis diagrams. (a) SO42 (b) S2O32 (c) SbF3 (d) SCNarrow_forward
- The two compounds nitrogen dioxide and dinitrogen tetraoxide are introduced in Section 3.13. (a) NO2 is an odd-electron compound. Draw the best Lewis diagrams possible for it, recognizing that one atom cannot achieve an octet configuration. Use formal charges to decide whether that should be the (central) nitrogen atom or one of the oxygen atoms. (b) Draw resonance forms for N2O4 that obey the octet rule. The two N atoms are bonded in this molecule.arrow_forward(b) The Murchison meteorite that landed in Australia in 1969 contained 92 different amino acids, including 21 found in Earth organism A skeleton structure (single bond only) of one of these extraterrestrial amino acids is shown below. Draw a Lewis structure, and identify any atoms having a nonzero formal charge. H3N. C ČH2 ČH3 (c) Draw the orbital diagrams and Lewis symbols to depict the formation of Na* and CI ions from the atoms. Give the formula of the compound formed. (d) The predicted bond length for HF is 109 pm (the sum of the covalent radii of H, 37 pm and F, 72 pm), however the actual bond length for HF is shorter (92 pm). It was observed that the difference between predicted and actual bond lengths becomes smaller going down the halogen group from HF to HI Describe these observationsarrow_forward8D.4. Benzene, a common solvent, is a covalent molecular compound which contains only carbon and hydrogen. Its simplest (empirical) formula is CH, and its molecular weight is 78 g/mol to 2 significant digits. What is its molecular formula? 8D.5. Draw the Lewis Dot Structure of (a) phosphorus pentafluoride. What is the formal charge on all atoms? (b) the perchlorate ion- in this case expand the octet for the chlorine atom in order to optimize the formal charges.arrow_forward
- (a) Determine the formal charge of oxygen in the following structure. If the atom is formally neutral, indicate a charge of zero. (b) Draw an alternative Lewis (resonance) structure for the compound given in part (a). Show the unshared pairs and nonzero formal charges in your structure. Don't use radicals. Formal charge on O 0arrow_forwardFor the next compounds/ions, draw two (2) appropriate Lewis structures. One structure must obey the octet rule and the other structure must be a non-octet obeying structure (octet deficient or octet expansion). Be sure to indicate which structure is the “best” structure and explain your choice formal charge arguments and any other points you deem important. (a) BeCl2 (b) POF3 (c) SO42−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
- Diazomethane is a highly poisonous, explosive compound because it readily evolves N2. Diazomethane has the following composition by mass: 28.57% C; 4.80% H; and 66.64% N. The molar mass of diazomethane is 42.04 g>mol. Find the molecular formula of diazomethane, draw its Lewis structure, and assign formal charges to each atom. Why is diazomethane not very stable? Explain.arrow_forward3.) Draw the two possible Lewis structures for acetamide, H₂CCONH2. Calculate the formal charge on each atom in each structure and use formal charge to indicate the more likely structure. Label all bonds as being polar or nonpolar.arrow_forward(a) Compare the bond enthalpies (Table 8.3) of the carbon–carbon single, double, and triple bonds to deduce an averageπ -bond contribution to the enthalpy. What fraction ofa single bond does this quantity represent? (b) Make a similarcomparison of nitrogen–nitrogen bonds. What do youobserve? (c) Write Lewis structures of N2H4, N2H2, and N2,and determine the hybridization around nitrogen in eachcase. (d) Propose a reason for the large difference in yourobservations of parts (a) and (b).arrow_forward
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