Answer the followings BY EQUATIONS:1. Starting from 2-bromopropane prepare Three from the followings;a. Propeneb. Propanolc. 2-Propanold. Chloropropanee. Acetic acidf. Propane2. An alkene compound with general formula C4H8 was treated with hot potassiumpermanganate (KMnO4). The main product in the reaction mixture was acetic acid(CH3COOH). What is the chemical structure of that alkene?

Answered: Image /qna-images/answer/873cbf4a-dbca-4517-b29e-dea99e6fac28.jpg

Answered: Answer the followings BY EQUATIONS: 1.…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Reagents a. CeHsCHO b. NaOH, ethanol c. Pyrrolidine, cat. H* j. Brz, H* d. H2C=CHCN e. H3O* f. h. BRCH2CH=CH2 i. Na* OEt, ethanol k. K* t-Buo I. CH2(CO,Et)2 m. heat CH2CH2CN LDA g. ELOC(=0)COEt Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda).
projector=1 5. 2-pentanol d. 2-methyl-2-butanol Ethanoic acid (vinegar) when diluted to low concentrations by water can be prepared from 15. ethene by a. reduction with H2, followed by reaction with a strong oxidizer b. addition of HCI, followed by reaction with H,O c. addition of H2O followed by reaction with a strong oxidizer d. addition of Br2, followed by reduction with H2 16. The primary product of the reaction below which uses excess HBr is which of the following? HBr C. Br Br Br Br b. d. Br Br Br Br Br Br 17. Select the compound with the highest boiling point at standard pressure. a. d. CH4 носн,сн,он b. е. CH 3CH 2CH 3 H3C-CH-CH3 он с. CH 3 CH 20H 18. One of the ingredients on a margarine container is listed as "polyunsaturated corn oil". This means that a. many of the carbon-c Page b. many of the polymer 3 l7tiple- urited
1. Fill in the boxes with the missing reagents or major organic products for the alkene reactions. a. HCl b. H2O, H2SO4 с. d. 1. ВН, 2. H2O2, NaOH е. f. CI .CI g. Cl2, H2O h. 1. Н-О, Hg(OАс)2 2. NaBH4, NaOH i. 1. O3 2. Н:0, H-02 j. OH HO.
Pp.30. Subject :- Chemistry
CH2 H3C H3C COOH Reagents e. PB13 f. NaCN then H3O* g. NBS, CCI4 h. CrO3, H2SO4 а. HBr b. Mg, ether c. CO2, ether then H3O* d. BH3, THF then H2O2, OH"
7) You want to synthesize 3-methyl-2-pentene from 2-chloro-3-methylpentane. Which reagent would you use? a. HCI, heat b. NH:(aq), 25°C c. CH:CO2NA, CH:CO2H, heat d. CH3CH2ONA, CH3CH2OH, heat e. CН:CH2ОН, heat
40. Deuterium oxide, D20, is water that contains the stable hydrogen isotope 2H, usually shown as D. When dissolved in deuterium oxide, ethanol undergoes the following reaction: * CH3CH2OH + D½0 → CH;CH2OD + HOD What is the best way of showing that this reaction has occurred? A. By testing the product with phosphorus pentachloride and not getting steamy fumes. B. By determining the mass spectrum of the mixture and showing peaks at m/z values of 20 and 46. C. By fractionally distilling the mixture and determining the amount of CH3CH2OD using a Geiger counter. D. By determining the mass spectrum of the mixture and showing peaks at m/z values by 19 and 47. A В O D
compound c compound f Reagents compound e a. HBr m. 2 equivalents of NaNH2 b. HBr, H2O2, hv H2, Lindlar's catalyst Na / NH3 H2SO4, H9SO4 (sia)2BH then H2O2, NaOH n. m c. H2O, H2SO4 d. Br2 e. Cl2 f. H2, Pd g. Br2, H20 h. Cl2, H2O i. O. d. compound b compound d p. q. 1 equivalent of NANH2 r. S. NBS, hv compound a Br2, hy Cl2, hy t. Os04 then NaHSO3 j. Hg(OAc)2, H2O then NaBH4 k. BH3 then H2O2, NaOH I. u. V. HCI w. (CH3)3CO'K* Og then (CH3)2S The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compound c.
6. Which of the following alcohols is oxidized to a ketone by chromic acid? I. II. III. I. II. OH III. OH CH₂OH 7. What are the major organic products when the following molecule is treated with ozone, and then with Zn/H2O? CH₂ Yu A. I B. II C. III D. IV E. V ,COH O IV. H-C-H IV. COOH V. 2 CH₂O CH₂OH CH₂ C-CH3 OH V. -OH Jº. n&on но- -он Y. A. I B.II C.III D.IV E. V 8. What compound results when 1-heptyne undergoes ozonolysis? A. heptanal B. 2-heptanone C. heptanoic acid D. hexanoic acid and CO2 E. 1-heptanol
Reagents a. CeHsCHO b. NaOH, ethanol c. Pyrrolidine, cat. H* d. H2C=CHCN e. H30* f. LDA g. ELOC(=0)CO,Et h. BRCH2CH=CH2 Na* OEt, ethanol j. Br2, H* k. K* t-BuO 1. CH2(CO2Et)2 m. heat Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda). Submit Answer Try Another Version 1 Item attempt remaining
Which reagent is appropriate for the following reaction. Cyclohexene converted to trans-cyclohexane diol. A. KMNO4, cold, neutral B. 1. OsO4/2. NaHSO3, H2O С. 1. RCOOОН/2. ОН- D. HIO4
2-Methyl-2-butene reacts with HBr in the presence of peroxide to give a. a secondary alkyl bromide. b. a primary alkyl bromide. c. a tertiary alkyl bromide. d. a vicinal dibromide.

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