HC=CH Reagents available a. HCI e. На, Рd i. H2 / Lindlar's catalyst b. HBr f. OsO4 then NaHSO3 j. Na / NH3 с. Вг2 g. O3 then (CH3)2S k. (sia)2 BH then H2O2, NaOH d. Cl2 h. 2 equivalents of NaNH2 1. 1 equivalent of NaNH2 The above synthesis scheme was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this scheme, identify the reagents necessary to accomplish the following steps in the production of (3R,4S)-3,4-dibromohexane from acetylene: Step 4: Step 1: Step 3 :

HC=CH Reagents available a. HCI e. На, Рd i. H2 / Lindlar's catalyst b. HBr f. OsO4 then NaHSO3 j. Na / NH3 с. Вг2 g. O3 then (CH3)2S k. (sia)2 BH then H2O2, NaOH d. Cl2 h. 2 equivalents of NaNH2 1. 1 equivalent of NaNH2 The above synthesis scheme was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this scheme, identify the reagents necessary to accomplish the following steps in the production of (3R,4S)-3,4-dibromohexane from acetylene: Step 4: Step 1: Step 3 :

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...

See similar textbooks

Similar questions

What are the products of the following reactions?
From the table of reagents shown below, show how you synthesize the product from the given reactant. H3C NO₂ a. NBS, (PhCO₂), b. Bra, FeBr, c. Br₂, H d. OH e. NaOH(s), A 1. HNO₂, H₂SO 9. H₂ CrO Answer: NO₂ Reagents available. h. CH, CI, AICI, o. CuCN 1. CH₂ CH₂ Br p. H₂O, A 1. CH₂O, A q. CH₂ CH₂ COCI, AICI, k. CH, COCI, AICI r. H₂NNH,, OH A 1. Mg, Et₂0 s. H₂. Pd/C m. CO₂ (s) then H₂0 t. H₂PO, n. HONO 0°C u. Cl₂, FeCla (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Previous Next
12. Give the starting materials or products (whatever is missing) for the following reactions: a. CH3C(CH2)3CCH3 b. 12 b. || NaOH(aq) heat OH- heat H2/Pd-C CH3CH2CH2CHCHO CH3 A Grignard reagent that is a key intermediate in the industrial synthesis of vitamin A can be prepared in the following way: 1. liq NH3 H3O+ 2 C2H5MgBr A (CHO) B HO C (C6H6Mg2Br₂O) Li 2. NH
Reagents CH3 a. HNO3, H2SO4 f. CH3OH LOCH3 b. SnCl2, H3O+ then NaOH(aq) g. CuCN C. HNO2, HCI h. Nal d. HBF4 i. LIAIH4 then H₂O e. KMnO4 j. CH3COCI Choose reagents from the table to synthesize this compound from toluene. Enter the letters in the order that you wish to use the reagents, without spaces or punctuation, i.e. 'adeg'. Submit Answer Try Another Version 2 item attempts remaining Visited
Match the reactions with their products below. HAI(OIBU)3 1. a.) CI 1.) NABH4 2. b.) H. 2.) H3O* 3. (CH3),CuLi c.) OH 4. CH3OH d.) EtgN 5. HN(CH3)2 e.) EtgN
Reagents a. HBr m. 2 equivalents of NaNH2 b. HBr, H2O2, hv c. H20, H2SO4 d. Br2 H2, Lindlar's catalyst Na / NH3 H2SO4, H9SO4 (sia)2BH then H2O2, NaOH n. O. 5 р. е. Cl q. 1 equivalent of NANH2 H2, Pd g. Br2, H2O h. Cl2, H2O OsO4 then NaHSO3 j. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH Og then (CH3)2S f. r. S. NBS, hv Br2, hv Cl2, hv t. i. u. V. HCI I. 2 Previous Next
Which is a possible product of the reaction below?
Fill in the missing reagents. It MAY take more than one step. a. SOH Br b. Br Cl NH2 CI CI CI Br Br
Complete the following reactions
O O X10. Predict the product for the following reaction. O COCH 3 I VI 1. LiAlH4 2. H₂O CH2OH COCH 3 meth CH2OH A. B C. D. I and II E. I and III H- HO II H HO III
NC. HOOC NC. OCH₂CH3 CN IV COOH COOH F OH NC. Reactant-Reagent NO₂ CN HO3S OCH₂CH3 II fuming H₂SO4 CN NaOCH₂CH3 heat hot KMnO4 NO₂ OH SO₂H VI NO₂ V OH COOH COOH Product
Determine the major product of the rxn 1. PB13 (CH3)2CHCH,OH 2. Mg/ether 3. ерохide/H+ а. b. HO. OH OH с. d.