EBK PRINCIPLES OF MODERN CHEMISTRY
8th Edition
ISBN: 9781305465091
Author: Butler
Publisher: YUZU
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Chapter 1, Problem 5P
A sample of ascorbic acid (vitamin C) is synthesized in the laboratory. It contains 30.0 g carbon and 40.0 g oxygen. Another sample of ascorbic acid, isolated from lemons (an excellent source of the vitamin), contains 12.7 g carbon. Compute the mass of oxygen (in grams) in the second sample.
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Draw the stepwise mechanism for the reactions
Part I.
a)
Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone
b) Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone
(3,3-dimethyl-2-butanone) and 2, 3-dimethyl - 1,3-butadiene. Give reasonable mechanism
the formation of
the products
For
3. The explosive decomposition of 2 mole of TNT (2,4,6-trinitrotoluene) is shown below:
Assume the C(s) is soot-basically atomic carbon (although it isn't actually atomic carbon in real life).
2
CH3
H
NO2
NO2
3N2 (g)+7CO (g) + 5H₂O (g) + 7C (s)
H
a. Use bond dissociation energies to calculate how much AU is for this reaction in kJ/mol.
Chapter 1 Solutions
EBK PRINCIPLES OF MODERN CHEMISTRY
Ch. 1 - Classify the following materials as substances or...Ch. 1 - Classify the following materials as substances or...Ch. 1 - A 17th-century chemist wrote of the “simple bodies...Ch. 1 - Since 1800, almost 200 sincere but erroneous...Ch. 1 - A sample of ascorbic acid (vitamin C) is...Ch. 1 - A sample of a compound synthesized and purified in...Ch. 1 - Nitrogen (N) and silicon (Si) form two binary...Ch. 1 - Iodine (I) and fluorine (F) form a series of...Ch. 1 - Vanadium (V) and oxygen (O) form a series of...Ch. 1 - Prob. 10P
Ch. 1 - Prob. 11PCh. 1 - Prob. 12PCh. 1 - Pure nitrogen dioxide (NO2) forms when dinitrogen...Ch. 1 - Gaseous methanol (CH3OH) reacts with oxygen (O2)...Ch. 1 - In J. J. Thompson’s experiment depicted in Figures...Ch. 1 - In the problem 15 above, what is vy , the...Ch. 1 - The natural abundances and isotopic masses of the...Ch. 1 - The natural abundances and isotopic masses of the...Ch. 1 - Prob. 19PCh. 1 - More than half of all the atoms in naturally...Ch. 1 - The isotope of plutonium used for nuclear fission...Ch. 1 - The last “missing” element from the first six...Ch. 1 - Prob. 23PCh. 1 - In 1982, the production of a single atom of...Ch. 1 - Prob. 25PCh. 1 - Prob. 26PCh. 1 - Compute the relative molecular masses of the...Ch. 1 - Prob. 28PCh. 1 - Suppose that a person counts out gold atoms at the...Ch. 1 - A gold atom has a diameter of 2.881010m . Suppose...Ch. 1 - The vitamin A molecule has the formula C20H30O ,...Ch. 1 - Arrange the following in order of increasing mass:...Ch. 1 - Mercury is traded by the “flask,” a unit that has...Ch. 1 - Gold costs $400 per troy ounce, and...Ch. 1 - Aluminum oxide (Al2O3) occurs in nature as a...Ch. 1 - Prob. 36PCh. 1 - Soft wood chips weighing 17.2 kg are placed in an...Ch. 1 - In a reproduction of the Millikan oil-drop...Ch. 1 - A rough estimate of the radius of a nucleus is...Ch. 1 - In a neutron star, gravity causes the electrons to...Ch. 1 - Prob. 41APCh. 1 - Naturally occurring rubidium (Rb) consists of two...Ch. 1 - A sample of a gaseous binary compound of boron and...
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- Part I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone and (3,3-dimethyl-2-butanone) 2,3-dimethyl-1,3-butadiene. Give reasonable mechanism the formation of the products Forarrow_forwardShow the mechanism for these reactionsarrow_forwardDraw the stepwise mechanismarrow_forward
- Draw a structural formula of the principal product formed when benzonitrile is treated with each reagent. (a) H₂O (one equivalent), H₂SO₄, heat (b) H₂O (excess), H₂SO₄, heat (c) NaOH, H₂O, heat (d) LiAlH4, then H₂Oarrow_forwardDraw the stepwise mechanism for the reactionsarrow_forwardDraw stepwise mechanismarrow_forward
- Part I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: a) Give the major reason for the exposure of benzophenone al isopropyl alcohol (w/acid) to direct sunlight of pina colone Mechanism For b) Pinacol (2,3-dimethy 1, 1-3-butanediol) on treatment w/ acid gives a mixture (3,3-dimethyl-2-butanone) and 2, 3-dimethyl-1,3-butadiene. Give reasonable the formation of the productsarrow_forwardwhat are the Iupac names for each structurearrow_forwardWhat are the IUPAC Names of all the compounds in the picture?arrow_forward
- 1) a) Give the dominant Intermolecular Force (IMF) in a sample of each of the following compounds. Please show your work. (8) SF2, CH,OH, C₂H₂ b) Based on your answers given above, list the compounds in order of their Boiling Point from low to high. (8)arrow_forward19.78 Write the products of the following sequences of reactions. Refer to your reaction road- maps to see how the combined reactions allow you to "navigate" between the different functional groups. Note that you will need your old Chapters 6-11 and Chapters 15-18 roadmaps along with your new Chapter 19 roadmap for these. (a) 1. BHS 2. H₂O₂ 3. H₂CrO4 4. SOCI₂ (b) 1. Cl₂/hv 2. KOLBU 3. H₂O, catalytic H₂SO4 4. H₂CrO4 Reaction Roadmap An alkene 5. EtOH 6.0.5 Equiv. NaOEt/EtOH 7. Mild H₂O An alkane 1.0 2. (CH3)₂S 3. H₂CrO (d) (c) 4. Excess EtOH, catalytic H₂SO OH 4. Mild H₂O* 5.0.5 Equiv. NaOEt/EtOH An alkene 6. Mild H₂O* A carboxylic acid 7. Mild H₂O* 1. SOC₁₂ 2. EtOH 3.0.5 Equiv. NaOEt/E:OH 5.1.0 Equiv. NaOEt 6. NH₂ (e) 1. 0.5 Equiv. NaOEt/EtOH 2. Mild H₂O* Br (f) i H An aldehyde 1. Catalytic NaOE/EtOH 2. H₂O*, heat 3. (CH,CH₂)₂Culi 4. Mild H₂O* 5.1.0 Equiv. LDA Br An ester 4. NaOH, H₂O 5. Mild H₂O* 6. Heat 7. MgBr 8. Mild H₂O* 7. Mild H₂O+arrow_forwardLi+ is a hard acid. With this in mind, which if the following compounds should be most soluble in water? Group of answer choices LiBr LiI LiF LiClarrow_forward
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