Chemistry by OpenStax (2015-05-04)
1st Edition
ISBN: 9781938168390
Author: Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher: OpenStax
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Textbook Question
Chapter 19, Problem 6E
Which of the following is the strongest oxidizing agent: VO43, CrO42-, or MnO4-?
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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
For
Show the mechanism for these reactions
Draw the stepwise mechanism
Chapter 19 Solutions
Chemistry by OpenStax (2015-05-04)
Ch. 19 - Write the electron configurations far each of the...Ch. 19 - Write the electron con?gurations for each of the...Ch. 19 - Write the electron configurations for each of the...Ch. 19 - Why are the lanthanoid elements not found in...Ch. 19 - Which of the following elements is most likely to...Ch. 19 - Which of the following is the strongest oxidizing...Ch. 19 - Which of the following elements is most likely to...Ch. 19 - The following reactions all occur in a blast...Ch. 19 - Why is the formation of slag useful during the...Ch. 19 - Would you expect an aqueous manganese (VII) oxide...
Ch. 19 - Iron (II) can be oxidized to iron (III) by...Ch. 19 - How many cubic feet of air at a pressure of 760...Ch. 19 - Find the potentials of the following...Ch. 19 - A 2.5624-g sample of a pure solid alkali metal...Ch. 19 - The standard reduction potential for the reaction...Ch. 19 - Predict the products of each of the following...Ch. 19 - Predict the products of each of the following...Ch. 19 - Describe the electrolytic process for refining...Ch. 19 - Predict the products of the following reactions...Ch. 19 - What is the gas produced when iron(II) sulfide is...Ch. 19 - Predict the products of each of the following...Ch. 19 - Balance the following equations by...Ch. 19 - Dilute sodium cyanide solution is slowly dripped...Ch. 19 - Predict which will be more stable, [CrO4]2- or...Ch. 19 - Give the oxidation state of the metal for each of...Ch. 19 - Indicate the coordination number for the central...Ch. 19 - Give the coordination numbers and write the...Ch. 19 - Give the coordination number for each metal ion in...Ch. 19 - Sketch the structures of the following complexes....Ch. 19 - Draw diagrams for any Cis, trans, and optical...Ch. 19 - Name each of the compounds or ions given in...Ch. 19 - Name each of the compounds or ions given in...Ch. 19 - Specify whether the following complexes have...Ch. 19 - Predict whether the carbonate ligand CO32- will...Ch. 19 - Draw the geometric, linkage, and ionization...Ch. 19 - Determine the number of unpaired electrons...Ch. 19 - Draw the Crystal field diagrams for [Fe(NO2)6]4-...Ch. 19 - Give the oxidation state of the metal, number of d...Ch. 19 - The solid anhydrous solid CoCl2 is blue in color....Ch. 19 - Is it possible for a complex of a metal in the...Ch. 19 - How many unpaired electrons are present in each of...Ch. 19 - Explain how the diphosphate ion, [O3P-O-PO3]4-,...Ch. 19 - For complexes of the same metal ion with no change...Ch. 19 - Trimethylphosphine, P(CH3)3, can act as a ligand...Ch. 19 - Would you expect the complex [Co(en)3]Cl3 to have...Ch. 19 - Would you expect the Mg3[Cr(CN)5]2 to be...Ch. 19 - Would you expect salts of the gold(I) ion, Au+, to...Ch. 19 - [CuCl4]2- is green. [Cu(H2O)6]2+ is blue. Which...
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Similar questions
- 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
- Q4: Write organic product(s) of the following reactions and show the curved-arrow mechanism of the reactions. Br MeOH OSO2CH3 MeOHarrow_forwardProvide the correct IUPAC name for the compound shown here. Reset cis- 5- trans- ☑ 4-6- 2- 1- 3- di iso tert- tri cyclo sec- oct but hept prop hex pent yl yne ene anearrow_forwardQ6: Predict the major product(s) for the following reactions. Note the mechanism (SN1, SN2, E1 or E2) the reaction proceeds through. If no reaction takes place, indicate why. Pay attention to stereochemistry. NaCN DMF Br σ Ilm... Br H Br H H NaCN CH3OH KOtBu tBuOH NaBr H₂O LDA Et2O (CH3)2CHOH KCN DMSO NaOH H₂O, A LDA LDA Systemarrow_forward
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