6. Which of the following will yield this compound (image below) when heated with potassium bisulfate? Click all answers that apply to get score. * H H H. Water Butanol Clove oil Peanut oil Peppermint oil 7. Which of the following will absorb and decolorize the highest amount of iodine solution? Click all answers that apply to get score. * Water Butanol Clove oil Peanut oil Peppermint oil

6. Which of the following will yield this compound (image below) when heated with potassium bisulfate? Click all answers that apply to get score. * H H H. Water Butanol Clove oil Peanut oil Peppermint oil 7. Which of the following will absorb and decolorize the highest amount of iodine solution? Click all answers that apply to get score. * Water Butanol Clove oil Peanut oil Peppermint oil

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).
What is the product? CALA © B. C OC. D OD. B MeO₂C A. CO₂Me H MeO₂C. ಚಿಕ C. MeO₂C B. MeO₂C. D.
A. Mel B B. Na, NH3 (1) C. Br2, hv Transformation A: A D L D. NaNH2 E. H₂, Lindlar's cat. F. H₂, Pt G. HBr (1 equiv.) H. 1) xs NaNH2; 2) H,O I. 1) RCO3H; 2) H3O+ Transformation B:
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
1 mole Br CC4 2 moles H,/Pt 1 mole H2 Lindlar's cataly st 2HC1 NANH, CH3C=CH 1. disiamylborane 2. HO ,H,O2,H2O 2HBR H2SO4,HgSO4 Peroxide a. b b. C С. d. e e. f
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.
Chapter 11 CH3 O H3C-CH-C-Br Type of finecional group AC4 habde Bomide) C. Type of functional group. CH3 H3C-CH 2 -Br 3 IUPAC CH, O H3C-CH-C-Br Common Name Acid Anhydnde H30 -CH3 Type of functional group. methexy methiny H3C-C -C-CH3 IUPAC H3C CH3 Common Name
nurbuks alixir 9 and lead). solution of ammonium chloride ) (~Hyl) acetate (Pb(CH3006) ₂ This solid? produces a solid. What is the identity of Bott A. Pb (CH₂COO), B. Pb (NH4)₂ C. (NH4), 4 D) Pb C (W) J Ẹ NH, CH, Coo Expl 49 42-0 CO C-PF St LGO (23 21 HO SA R الموت id boke slit + CXIC moth SHMOB stata G
please make the explanation clear and thank you for your help
4. Draw structures for products of the following reactions. PaCl, (Bu water tBu PdCI, methanol OH CHCI, NaOH, water Me,N LDA, THE, 0°C BulI (2 moles) Bri THF, -78°C Buli THE, °C Br Pd(OAch THE, 0C MeO
Predict the complete products for the following reactions of hydrocarbons and alcohols. Indicate NR if there is NO REACTION
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.