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EP GENERAL CHEMISTRY-MOD.MASTERINGCHEM.
11th Edition
ISBN: 9780133897340
Author: Petrucci
Publisher: PEARSON CO
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Textbook Question
Chapter 11, Problem 44E
In which of the following ions would you expect to find delocalized molecular orbitals? Explain. (a)
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Chapter 11 Solutions
EP GENERAL CHEMISTRY-MOD.MASTERINGCHEM.
Ch. 11 - Prob. 1ECh. 11 - Explain why it is necessary to hybridize atomic...Ch. 11 - Describe the molecular geometry of H2O suggested...Ch. 11 - Describe the molecular geometry of NH2 suggested...Ch. 11 - In which of the following, CO32-,SO2,CCl4,CO,NO3-...Ch. 11 - In the manner of Example 11-1, describe the...Ch. 11 - For each of the following species, identify the...Ch. 11 - Propose a plausible Lewis structure, geometric...Ch. 11 - Describe a hybridization scheme for the central Cl...Ch. 11 - Describe a hybridization scheme for the central S...
Ch. 11 - Match each of the following species with one of...Ch. 11 - Propose a hybridization scheme to account for...Ch. 11 - Indicate which of the following molecules and ions...Ch. 11 - In the manner of Figure 11-18, indicate the...Ch. 11 - Write Lewis structures for the following...Ch. 11 - Represent bonding in the carbon dioxide molecule,...Ch. 11 - Use the method of Figure 11-19 to represent...Ch. 11 - Use the method of Figure 11-19 to represent...Ch. 11 - The molecular model below represents citric acid,...Ch. 11 - Malic is e common organic acid found in unripe...Ch. 11 - Shown below are ball-and-stick models. Describe...Ch. 11 - Shown below are ban-and-stick models. Describe...Ch. 11 - Prob. 23ECh. 11 - The structure of the molecule allene, CH2CCH2 , is...Ch. 11 - Angelic acid, shown below, occurs in symbol root,...Ch. 11 - Dimethylolpropionic acid, shown below, is used in...Ch. 11 - Explain the essential difference in how the...Ch. 11 - Describe the bond order of diatomic carbon, C2 ,...Ch. 11 - Prob. 29ECh. 11 - The paramagnetism of gaseous B2 has been...Ch. 11 - Prob. 31ECh. 11 - Is it correct to say that when a diatomic molecule...Ch. 11 - For the following pairs of molecular orbitals,...Ch. 11 - For each of the species C2+,O2,F2+ , and NO+ ; a....Ch. 11 - Write plausible molecular orbital occupancy...Ch. 11 - We have used the term “isoelectronic” to refer to...Ch. 11 - Consider the molecules NO+ and N2+ and use...Ch. 11 - Consider the molecules CO+ and CN- and use...Ch. 11 - Construct the molecular orbital diagram for CF....Ch. 11 - Construct the molecular orbital diagram for SrCl....Ch. 11 - Explain why the concept of delocalized molecular...Ch. 11 - Explain how it is possible to avoid the concept of...Ch. 11 - In which of the following molecules would you...Ch. 11 - In which of the following ions would you expect to...Ch. 11 - The Lewis structure of N2 indicates that the...Ch. 11 - Show that both the valence bond method and...Ch. 11 - A group of spectroscopists believe that they have...Ch. 11 - Lewis theory is satisfactory to explain bonding in...Ch. 11 - The compound potassium sesquoxide has the...Ch. 11 - Draw a Lewis structure for the urea molecule, CO(...Ch. 11 - Methyl nitrate, CH2NO2 , is used as a rocket...Ch. 11 - Fluorine nitrate, FONO2 , is an oxidizing agent...Ch. 11 - Draw a Lewis structure(s) for the nitrite ion, NO2...Ch. 11 - Think of the reaction shown here as involving the...Ch. 11 - Prob. 55IAECh. 11 - Prob. 56IAECh. 11 - The molecule formamide, HCONH2 , has the...Ch. 11 - Pyridine, C2H2N , is used in the synthesis of...Ch. 11 - Prob. 59IAECh. 11 - The ion F2Cl is linear, but the ion F2Cl+ is bent....Ch. 11 - Prob. 61IAECh. 11 - Prob. 62IAECh. 11 - Prob. 63IAECh. 11 - Prob. 64IAECh. 11 - Histidine, an essential amino acid, serves as a...Ch. 11 - The anion I42 is linear, and the anion I5 is...Ch. 11 - Prob. 67IAECh. 11 - A conjugated hydrocarbon has an alternation of...Ch. 11 - An elusive intermediate of atmospheric reactions...Ch. 11 - Resonance energy is the difference in energy...Ch. 11 - Furan, C4H4O , is a substance derivable from oat...Ch. 11 - As discussed in Are You Wondering 11-1, the sp...Ch. 11 - In Chapter 10, we saw that electronegativity...Ch. 11 - Borazine, B2N2H2 is often referred to as inorganic...Ch. 11 - Which of the following combinations of orbitals...Ch. 11 - Prob. 76FPCh. 11 - Prob. 77SAECh. 11 - Prob. 78SAECh. 11 - Explain the important distinctions between the...Ch. 11 - A molecule in which sp2 hybrid orbitals are used...Ch. 11 - Prob. 81SAECh. 11 - The hybridization scheme for the central atom...Ch. 11 - Of the following, the species with a bond order of...Ch. 11 - The hybridization scheme for Xe in XeF2 is (a) sp;...Ch. 11 - Delocalized molecular orbitals are found in (a)...Ch. 11 - Prob. 86SAECh. 11 - Why does the hybridization sp2d not account for...Ch. 11 - What is the total number of (a) bonds and (b) p...Ch. 11 - Which of the following species are paramagnetic?...Ch. 11 - Use the valence molecular orbital configuration to...Ch. 11 - Use the valence molecular orbital configuration to...Ch. 11 - Which of these diatomic molecules do you think has...Ch. 11 - For each of the following ions or molecules,...Ch. 11 - Draw Lewis structures for the NO2 and NO2+ ions,...Ch. 11 - In which of the following is the central atom sp...Ch. 11 - Prob. 96SAECh. 11 - According to molecular orbital theory, the O22 ion...Ch. 11 - What is the angle between the hybrid orbitals...Ch. 11 - Consider the molecule with the Lewis structure...Ch. 11 - Construct a concept map that embodies the ideas of...Ch. 11 - Prob. 101SAECh. 11 - Construct a concept map that describes the...
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- Please solvearrow_forwardRank the compounds in each group below according to their reactivity toward electrophilic aromatic substitution (most reactive = 1; least reactive = 3). Place the number corresponding to the compounds' relative reactivity in the blank below the compound. a. CH₂F CH3 F b. At what position, and on what ring, is bromination of phenyl benzoate expected to occur? Explain your answer. :0: C-O phenyl benzoate 6.Consider the reaction below to answer the following questions. A B C NO₂ FeBr3 + Br₂ D a. The nucleophile in the reaction is: BODADES b. The Lewis acid catalyst in the reaction is: C. This reaction proceeds d. Draw the structure of product D. (faster or slower) than benzene.arrow_forwardPart 2. A solution of 6.00g of substance B in 100.0mL of aqueous solution is in equilibrium, at room temperature, wl a solution of B in diethyl ether (ethoxyethane) containing 25.0 g of B in 50.0 mL 9) what is the distribution coefficient of substance B b) what is the mass of B extracted by shaking 200 ml of an aqueous solution containing 10g of B with call at room temp): i) 100 mL of diethyl ether ii) 50ml of diethyl ether twice iii) 25ml of diethyl ether four timesarrow_forward
- - Rank the following groups of compounds from most acidic (1) to least acidic (4). Place the number corresponding to the compound's relative rank in the blank below the structure. a. NO₂ NO₂ CH2CH2CH2CH2OH CH3 CH3CH2CHOH CH3CH2CH2CH2OH NO₂ CH3CHCH2CH2OH b. OH OH CH₂OH CO₂H HC CN CN CNarrow_forwardGive the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry a. H MgBr 1. ether 2. H₂O* 4 COH b. 1. LIAIH, ether 2. H₂O Choose the best reagent(s) for carrying out the following conversions from the list provided below. Place the letter of the best choice in the blank to the left of the conversion. Reagents may be used more than once. a. 1. CH3MgBr, ether 2. H3O+ NaOH b. 1. PBr3 2. C. 2. 1. (CH3)3SiCl, (CH3CH2)3N CH3MgBr, ether 3. H₂O*+ 2. H3O+ e. 1. p-TosCl, pyridine f. نها g. 2. NaOH CrO3, H₂SO4, H₂O 1. NaBH4, ethanol 2. H30* h. PCC, CH2Cl2 Ovoldo-6 a. b. OH OH H OH O any organicarrow_forwardDetermine the rate law for sodium thiosulfate from the following data: [Na2S2O3] Time (s) 0.0318 230. 0.0636 57.5arrow_forward
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- Propose syntheses of the following compounds starting with benzene or toluene. Assume ortho and isomers can be separated. a. b. O₂N- Cl COOH para 0. Propose syntheses to carry out each of the following conversions. Assume ortho and para isomers can be separated a. Br b. COOH CH3 NH₂ PABA (active ingredient in some sunscreens)arrow_forwardH3C H C=C CH3 H m-chloroperoxybenzoic acid CH2Cl2, rt C-C--. H3CH2CC H H3C CH3 Cl₂ H₂O NaOH H₂O D. S- E. CH3 H₂O₂, H₂O It CH₂O Na + CHI F. HI, H₂O heat G. 4 OH CH3CHCH3 + ICH2CH3 1. NaH (CH3)3COH (CH3)3 COCHCH2CH3 2. CH3arrow_forward5. Show how the ether below could be prepared from toluene and any other necessary reagents. Show all reagents and all intermediate structures. H3C- H3C- CI OCH2CH3arrow_forward
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