need help with last hw problems, please explain and the answers with it thank you 27....
need help on last hw problems, please explain and the answers thank you 6. Draw a structural formula for the major organic product of the reaction shown below. (CH2=CHCMa CuLi 7. Draw a structural formula for the major organic product of the reaction shown below. CuLi Draw structural formulas for organic products A and B. 8. Hао Mg В A H3CC=CH2 ether Br 1. Specify whether the tramsformation shown involves net oxidation of carbon, net reduction of carbon, or neither...
When the 2,7-dimethyl-4-octyne is treated with 2 moles (excess) HBr, the product(s) of the reaction is: CH-CH-CH-CH-CH-CH-CH-CH, B. CH3-CH-CH CH -CH2-CH-CH-CH; C CH-CH-CH2-C-CH3-CH-CH-CH н D. A mixture of a and b would be produced. A mixture of a, b, and e would be produced OB 0 0 0 Which of the following is the correct structure for 4-sec-butyl-1-heptyne? D. none of these OD What is the major organic product obtained from the following reaction? OH M CH,CH-CH-CH2=CH- 3 OH •...
13. (12 pts-4 pts each) Show how you could carry out th how you could carry out the following synthesis reactions by placing the letters corresponding to the appropriate reagents above each ar must be in the correct order to receive full credit. priate reagents above each arrow. The reagents A. HBr, ether B. Br2, CH2Cl2 C. Br2, H2O D. 1. Hg(OAC)2, H2O/THF 2. NaBH4 E. 1. BH3, THF 2. H2O2, OH F. H2SO4, H2O/HgSO4 G. NBS, hy H. H/Pd/C...
please help in answering all of the questions 15. Which is a propagation step in the peride-initiated hydrobromination of 1 butene? (A) CH,CH:CH-CH, HBr -- CH,CH.CH,CH,Br (B) CH.CH.CH-CH,+Br - CH CH.CHCH,Br (C) CH.CH,CH,CH*+ Br-CH,CH,CH.CH, Br (D) ROOR + CH,CH,CH=CH, - RO + KOH + CHỊCH,CH,CH, 35. Indicate which C-H bond has the lowest bond dissociation enthalpy (energy)? (A) H-CH(CH), (B) H-CH (C) H-C(CH,), (D) H-CH,CH, 37 d. Predict the major product for this reaction (A) (B) BE BE (C) Br...
(References) Choose one reagent from the Table to carry out the following conversions (Use letters from the table to specify reagents) Reagents available d. 1. Bry 2. KOH in ethanol a. H, Pt g. KMnO, /H0+ b. 1. NaNH in NH 2. CH3Br e. He / Lindlar catalysth. H,OH,SO4 Hg80 c. 1 equiv Br2 f. 1. BH, in THF 2. H, O, in NaOH i. Li in NH, CH-CH2-C=CH CH-CH2-C-CH - CC-CHE CH CHS Submit Answer Try Another Version tom...
How would you synthesize the following compound from acetylene and reagents in the table? Choose the most efficient route. Specify reagents using letters from the table, first reagent on the left. Example: ab H H CH3CH2CH2 CH2CH3 a. Br2 b. CH3CH I Reagents available d. CH3 CH2CH2CH2Br g. KOH/ ethanol e. Hy / Lindlar's catalyst | h. NaNH / NH3 f. 1. BHz in THF 2. H2O2 in NaOH c. CH3 CH, CH,Br Reagents (in order of use) are Submit...
Which of these anions would be the most nucleophilic towards methyl iodide in an ethanol solution? LI. CH,CH2-C- Which reagent would be best for carrying out this transformation он (B) HO",heat (C) HIO, N-H Cro,cr (PCC) @ C+--Ο- Which reaction sequence would accomplish this t- What is che best rearest or set of reagents to accomplish ICH CH (B) H2, Pd NBS HBr, peroxides (A) KMnO/KOH (B) MCPBA 5 Which series of reactions would best accomplish this 1eWhas is the...
need help with last hw problems please explain and the answers thank you The regiochemistry of oxymercuration/demercuration of alkenes is A. Anti-Markovnikov. B. Markovnikov. C. Subject to solvent effects. D. Unrelated to alkene structure. Which compound has a net molecular dipole? H HHH D. H HH B. ІН The correct IUPAC name for the compound shown below is A. (3E)-3,7-dimethyl-1,3,6-octatriene B. (3Z)-3,7-dimethyl-1,3,6-octatriene C. (3E,6E)-3,7-dimethyl-1,3,6-octatriene D. (3Z,6E)-3,7-dimethyl-1,3,6-octatriene • The correct IUPAC name for the compound shown below is A. (2E, 4E)-5-ethyl-2,4-heptadiene...
1. Calculate AH for each reaction using bond dissociation values. Determine if the reaction is exothermic or endothermic a. CH3CH2CH3 + Br2 — CHșCH,CH,-Br + HBr ОН + H₂O + HI 498 297 aaa 720 - 698 - 22 401 andiotamie Table 6.2 Bond Dissociation Energies for Some Common Bonds IA-B - A. + .B] Bond AH kJ/mol (kcal/mol) Bond AH kJ/mol kcal/mol) 456 569 431 H-Z bonds H-F H-CI H-Br H-1 Н-ОН (136) (103) (88) 368 297 498 (71)...
can someone explain these? I have difficulties eith mechanisms. thank you 10. For each of the following reactions, draw the structure of the major organic product in the box provided. Each numbered set of reagents above or below the arrow represents a complete separate reaction. For multi-step reactions, give only the structure of the final product a) KOCH,CH HOCH.CH b) кови KOtBu HOtBu OTS EtOAc ОТf - сн, -Br сн, снен, KOCH.CH HOCH.CH н DMF кон (alc) DMSO KOtBu Нова...