Chemistry & Chemical Reactivity
10th Edition
ISBN: 9781337399074
Author: John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher: Cengage Learning
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Chapter 9, Problem 16PS
What is the electron-pair and molecular geometry around the central S atom in sulfuryl chloride. SO2Cl2? What is the hybridization of sulfur in this compound?
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Chapter 9 Solutions
Chemistry & Chemical Reactivity
Ch. 9.1 - Use valence bond theory to describe the bonding in...Ch. 9.1 - Identify the hybridization of each underlined atom...Ch. 9.1 - Use valence bond theory to describe the bonding in...Ch. 9.2 - What is the electron configuration of the H2+ ion?...Ch. 9.2 - Could the anion Li2 exist? What is the ions bond...Ch. 9.2 - The cations O2+ and N2+ are formed when molecules...Ch. 9.3 - Photoelectron spectroscopy is s1milar to the...Ch. 9.3 - What is the energy of a photon with a wavelength...Ch. 9.3 - Using the accompanying figure, state which...Ch. 9.3 - The kinetic energy of an electron ejected from the...
Ch. 9.3 - The N2+ ions that are formed when electrons with...Ch. 9.3 - What is the empirical formula of Tynan purple?Ch. 9.3 - Butter yellow absorbs light with a wavelength of...Ch. 9.3 - Prob. 2.3ACPCh. 9 - Draw the Lewis structure for chloroform, CHCl3....Ch. 9 - Draw the Lewis structure for NF3. What are its...Ch. 9 - Draw the Lewis structure for hydroxylamine, H2NOH....Ch. 9 - Draw the Lewis structure for 1,...Ch. 9 - Draw the Lewis structure for carbonyl fluoride,...Ch. 9 - Draw the Lewis structure for acetamide, CH3CONH2....Ch. 9 - Specify the electron-pair and molecular geometry...Ch. 9 - Specify the electron-pair and molecular geometry...Ch. 9 - Prob. 9PSCh. 9 - What is the hybrid orbital set used by each of the...Ch. 9 - Draw the Lewis structures of the acid HPO2F2 and...Ch. 9 - Draw the Lewis structures of the arid HSO3F and...Ch. 9 - What is the hybridization of the carbon atom in...Ch. 9 - What is the hybridization of the carbon atoms in...Ch. 9 - What is the electron-pair and molecular geometry...Ch. 9 - What is the electron-pair and molecular geometry...Ch. 9 - Prob. 17PSCh. 9 - For each compound below, decide whether cis and...Ch. 9 - Molecular Orbital Theory (See Examples 9.49.6.)...Ch. 9 - Give the electron configurations for the ions Li2+...Ch. 9 - Calcium carbide, CaC2, contains the acetylide ion,...Ch. 9 - Platinum hexafluoride is an extremely strong...Ch. 9 - When sodium and oxygen react, one of the products...Ch. 9 - When potassium and oxygen react, one of the...Ch. 9 - Among the following, which has the shortest bond...Ch. 9 - Consider the following list of small molecules and...Ch. 9 - Prob. 27PSCh. 9 - The nitrosyl ion. NO+, has an interesting...Ch. 9 - These questions are not designated as to type or...Ch. 9 - What is the OSO angle and the hybrid orbital set...Ch. 9 - Sketch the resonance structures for the nitrite...Ch. 9 - Sketch the resonance structures for the nitrate...Ch. 9 - Sketch the resonance structures for the N2O...Ch. 9 - Compare the structure and bonding in CO2 and CO32...Ch. 9 - Numerous molecules are detected in deep space....Ch. 9 - Acrolein, a component of photochemical smog, has a...Ch. 9 - The organic compound below is a member of a class...Ch. 9 - The compound sketched below is acetylsalicylic...Ch. 9 - Phosphoserine is a less-common amino acid. (a)...Ch. 9 - Lactic acid is a natural compound found in sour...Ch. 9 - Cinnamaldehyde ocaus naturally in cinnamon oil....Ch. 9 - The ion Si2 was reported in a laboratory...Ch. 9 - The simple valence bond picture of O2 does not...Ch. 9 - Nitrogen, N2, can ionize to form N2+ or add an...Ch. 9 - Which of the homonuclear, diatomic molecules of...Ch. 9 - Which of the following molecules or ions are...Ch. 9 - Prob. 47GQCh. 9 - The structure of amphetamine, a stimulant, is...Ch. 9 - Menthol is used in soaps, perfumes, and foods. It...Ch. 9 - Prob. 50GQCh. 9 - Suppose you carry out the following reaction of...Ch. 9 - Ethylene oxide is an intermediate in the...Ch. 9 - The sulfamate ion, H2NSO3, can be thought of as...Ch. 9 - The compound whose structure is shown here is...Ch. 9 - Prob. 55ILCh. 9 - Carbon dioxide (CO2), dinitrogen monoxide (N2O),...Ch. 9 - Draw the two resonance structures that describe...Ch. 9 - Draw a Lewis structure for diimide, HNNH. Then,...Ch. 9 - Prob. 59SCQCh. 9 - Consider the three fluorides BF4, SiF4, and SF4....Ch. 9 - When two amino acids react with each other, they...Ch. 9 - What is the connection between bond order, bond...Ch. 9 - When is it desirable to use MO theory rather than...Ch. 9 - Show how valence bond theory and molecular orbital...Ch. 9 - Three of the four molecular orbitals for...Ch. 9 - Lets look more closely at the process of...Ch. 9 - Borax has the molecular formula Na2B4O5(OH)4. The...Ch. 9 - A model of the organic compound allene is shown...Ch. 9 - Prob. 69SCQCh. 9 - Prob. 70SCQCh. 9 - Bromine forms a number of oxides of varying...Ch. 9 - Prob. 72SCQCh. 9 - Urea reacts with malonic acid to produce...
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- Use the References to access important values if needed for this question. What is the IUPAC name of each of the the following? 0 CH3CHCNH₂ CH3 CH3CHCNHCH2CH3 CH3arrow_forwardYou have now performed a liquid-liquid extraction protocol in Experiment 4. In doing so, you manipulated and exploited the acid-base chemistry of one or more of the compounds in your mixture to facilitate their separation into different phases. The key to understanding how liquid- liquid extractions work is by knowing which layer a compound is in, and in what protonation state. The following liquid-liquid extraction is different from the one you performed in Experiment 4, but it uses the same type of logic. Your task is to show how to separate apart Compound A and Compound B. . Complete the following flowchart of a liquid-liquid extraction. Handwritten work is encouraged. • Draw by hand (neatly) only the appropriate organic compound(s) in the boxes. . Specify the reagent(s)/chemicals (name is fine) and concentration as required in Boxes 4 and 5. • Box 7a requires the solvent (name is fine). • Box 7b requires one inorganic compound. • You can neatly complete this assignment by hand and…arrow_forwardb) Elucidate compound D w) mt at 170 nd shows c-1 stretch at 550cm;' The compound has the ff electronic transitions: 0%o* and no a* 1H NMR Spectrum (CDCl3, 400 MHz) 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm 13C{H} NMR Spectrum (CDCl3, 100 MHz) Solvent 80 70 60 50 40 30 20 10 0 ppm ppm ¹H-13C me-HSQC Spectrum ppm (CDCl3, 400 MHz) 5 ¹H-¹H COSY Spectrum (CDCl3, 400 MHz) 0.5 10 3.5 3.0 2.5 2.0 1.5 1.0 10 15 20 20 25 30 30 -35 -1.0 1.5 -2.0 -2.5 3.0 -3.5 0.5 ppm 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppmarrow_forward
- Part I. a) Elucidate the structure of compound A using the following information. • mass spectrum: m+ = 102, m/2=57 312=29 • IR spectrum: 1002.5 % TRANSMITTANCE Ngg 50 40 30 20 90 80 70 60 MICRONS 5 8 9 10 12 13 14 15 16 19 1740 cm M 10 0 4000 3600 3200 2800 2400 2000 1800 1600 13 • CNMR 'H -NMR Peak 8 ppm (H) Integration multiplicity a 1.5 (3H) triplet b 1.3 1.5 (3H) triplet C 2.3 1 (2H) quartet d 4.1 1 (2H) quartet & ppm (c) 10 15 28 60 177 (C=0) b) Elucidate the structure of compound B using the following information 13C/DEPT NMR 150.9 MHz IIL 1400 WAVENUMBERS (CM-1) DEPT-90 DEPT-135 85 80 75 70 65 60 55 50 45 40 35 30 25 20 ppm 1200 1000 800 600 400arrow_forward• Part II. a) Elucidate The structure of compound c w/ molecular formula C10 11202 and the following data below: • IR spectra % TRANSMITTANCE 1002.5 90 80 70 60 50 40 30 20 10 0 4000 3600 3200 2800 2400 2000 1800 1600 • Information from 'HAMR MICRONS 8 9 10 11 14 15 16 19 25 1400 WAVENUMBERS (CM-1) 1200 1000 800 600 400 peak 8 ppm Integration multiplicity a 2.1 1.5 (3H) Singlet b 3.6 1 (2H) singlet с 3.8 1.5 (3H) Singlet d 6.8 1(2H) doublet 7.1 1(2H) doublet Information from 13C-nmR Normal carbon 29ppm Dept 135 Dept -90 + NO peak NO peak 50 ppm 55 ppm + NO peak 114 ppm t 126 ppm No peak NO peak 130 ppm t + 159 ppm No peak NO peak 207 ppm по реак NO peakarrow_forwardCould you redraw these and also explain how to solve them for me pleasarrow_forward
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