A and C for #5 4. (12 pts) What product is formed when each compound is...
Draw the major organic product when each compound is treated with Tollens' reagent. If no reaction occurs, draw the reactant. Reaction A Reaction BReaction C
Reactions and Reagents 17,37 Draw the product formed when pentanal (CH,CH,CH,CH,CHO) is treated with each reagent. With some reagents, no reaction occurs. a. NaBH. CH,OH e. Na,Cr,O, H,SO4, H,0 1. [1] (CH3)2CuLi; [2] HO b. [1] LIAIH[2] H,0 f. Ag,O, NH,OH J. [1] HCCN: (2] H,0 c. Hz. Pd-C g. (1] CHẠMgar, [2] HẠO k. [CH,CECLI: [2] H,0 d. PCC b. [1] CH, LH: (2] HẠO 1. The product in (a), then TBDMS-CI, Imidazole
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
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ii. Proposed a reasonable structure for the product (C8H62-) formed when the compound 1 below is treated with a strong base butyllithium. (5 pts) 2 C4H9LI 2Lit C3H62 + 2 C4H10 iii. a. Identify the product of the following reaction (8 pts) 1. strong base 2. CH3OCH,CI b. Explain what is involved in this reaction and why it is a reasonable process.
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Draw the product formed when 1-bromobutane is treated with cach reagent. 1. Li (2 equiv) 2. Mg in (CHCH2):0 solvent 3. Li (2 equiv), then Cul (0.5 equiv) 4. The answer in (a), then H;O 5. The answer in (b), then D20 6. The answer in (a), then CH,CCH Draw the product formed when (CH3CH2CH2CH2) CuLi is treated with each compound. In so cases, no reaction occurs. CHн, ,then H,O Draw the product formed when the a.ß-unsaturated ketone A is...
U3 xii. Draw the structure of the intermediate formed when an alkene undergoes epoxidation. If there is no intermediate in the reaction, write none. 3. (26 points) In each of the problem below, provide the reagent(s)s or draw in the structure of the MAJOR product as indicated. For products, be sure stereochemistry is clearly shown when appropriate. If no reaction is expected state No Reaction or write NR. For reagent(s), more than I set may be needed. U3 - ?...
9. (2 pts) Which is the major product formed when the compound shown below is heated? CH3CH2C-CHEC-OH 10. (2 pts) What is the IUPAC name for the following compound? H2N COOH 11. (4 pts each) For each reaction complete the following: 1. Name the starting compound(s). 2. Name the type of reaction 3. Complete the reaction and 4. Draw the final structures. a) CH3CH2CH2COOH + CH3CH2OH H+ → b) 0, + NaOH ?
3. Draw the organic product formed when 1-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs a KH c HBr d HCI e NaHCO r i 1) KH: 2) CH?CHIBr b NaCI
TsCl, pyridine 1TSCI, pyridine, 2) LiAlH Draw the major product formed when 2-pentanol is treated with each reagent(s) 1) H2SO4, A 2) O, 3) Zn, H2O 4. PCC a е b Jones Reagent (Chromic acid + acetone) НСІ 1) H.SO4, A Devise a synthesis of each compound from acetylene (HC= CH) and organic compounds containing two carbons or less. You may use any other required reagents CH, CHCH&CH 5. a CH CHCH-CH,ОН b CH CHCH,CHО cis CH CH2CH-CHCH CO>H d...