BrBrBr.BrBr`Br BrBrBrBrDecaBDECompound A: Deca BDEcompound B: product of trichloroethylene(TCE)and tryptamineNH'N'H.CCI,Instructions: Write out two different phase I reactions and one phase II reaction for B, ANDone reaction (Phase I or II) for A, using chemical structures.Please be organized, thank you.

Answered: Image /qna-images/answer/8531ccab-6dcc-47ec-b251-8c4085b285d7.jpg

Answered: Br Br Br. Br Br `Br Br Br Br Br DecaBDE…

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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d) When butane, CH3CH2CH2CH3 and bromine gas, Br2 is exposed to sunlight, monobrominated product are produced. The reaction equation is given below: Apabila butana, CH3CH2CH2CH3 dan gas bromin, Brz terdedah kepada cahaya matahari, produk pembrominan tunggal dihasilkan. Persamaan tindak balas diberikan di bawah: uv CH;CH2CH2CH3 + Br2 A + B i) State the type of reaction. Nyatakan jenis tindak balas tersebut. ii) What is the function of the sunlight in the reaction? Apakah fungsi cahaya matahari dalam tindak balas tersebut? ii) Draw the structure of monosubstituted products, A and B. Label the major product. Lukis struktur bagi hasil penukargantian tunggal, A dan B. Labelkan hasil utama. iv) Draw the propagation steps in the mechanism for the formation of the major product. Lukis langkah perambatan dalam mekanisma bagi pembentukan hasil utama.
HO. Q U H joglo A B C D KMnO4, NaOH cold H2SO4 H₂O 1. BH3-THF 2. H₂O2, NaOH 1. Hg(OAc) 2, H₂O 2. NaBH4, NaOH
What is(are) the major product(s) of the following reaction? 1. ВНз, THF . ............. 2. NaOH, H202 OH HO OH OH II HO II IV Select one: O II, II O II, IV O II, V O IV, V
I. Complete the reaction map below А. HO HO 2 H2/Pt cold KMNO4 3 Ck
Provide the major organic product of the following reaction. I. HNO3. H,SO, 2. Fe, HCI 3. NANO,, HCI 4. HBF, 5. KMNO4, A CHICH3)2
IV. Fill-in the missing the reactant, reagent, or major product. 1. Hg(OAc), , H2O 2. NABH, 1. BiologyEnvironmental S 1. OsO4, pyridine 2 NaHSO,, H,O он 3. 2.
Draw the structure(s) of the major organic product(s) of the following reaction. O N₂ HSO4 • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the sign from the drop-down menu. ● ? Cu₂O/Cu(NO3)2 in H₂O or H₂O, heat ChemDoodleⓇ ▼ #[ ] در
Question 20 (Mandatory) (5 points) Which of the following has(have) a higher oxidation state of carbon than the carbon in formaldehyde, H₂C=O? 1. CH3OH II. HCO₂H III. H₂CO3 ||| II and III I. II. and III
What is the product? CALA © B. C OC. D OD. B MeO₂C A. CO₂Me H MeO₂C. ಚಿಕ C. MeO₂C B. MeO₂C. D.
Reagents m. 2 equivalents of NaNH2 H2, Lindlar's catalyst Na / NH3 p. H2SO4, HgSO4 q. (sia)2BH then H2O2, NaOH 1 equivalent of NaNH2 a. HCI b. HBr n. c. H20, H2SO4 d. Br2 0. n Cl2 е. H2, Pd g. Br2, H20 h. Cl2, H2O f. r. compound a Os04 then NaHSO3 j. Hg(OAc)2, H20 then NABH4 k. BH3 then H2O2, NaOH Oz then (CH3)2S i. compound b I. The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis, reagents from the table (shown in blue) are used to carry out the indicated reactions. In the box below, draw the structure of compound b. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Consider E/Z stereochemistry of alkenes. • If more than one structure fits the description, draw them all. • If a compound is formed more than once, add another sketcher and draw it again. • If the reaction produces a racemic mixture, draw both stereoisomers. Separate structures with + signs from the drop-down menu.
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.
5. Complete the missing reactant and identify the type of reaction CaCO3-CaO+? a) b) ?? + 2AgNO3-2AgCl+Ca(NO3)2 c) ?? + H2SO4- BaSO4+2H++2Cl-.

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