Identify the best reagents and reaction intermediate by dragging the appropriate label to its position in the following reaction scheme.
Identify the best reagents and reaction intermediate by dragging the appropriate label to its position in...
Provide the missing compounds and reagents in the reaction scheme below. Map at NaOMe, MeOH Select answer 1. NaOMe, MeOH 2. NaOH 3. H30*, heat Select answer NaOMe, MeOH Previous ⓧ Give Up & View Solution O Check Answer e Next Exit Hint
In each reaction box, place the best reagent and Conditions from the list below. H C C H Br Br H2, Lindlar catalyst H20, H2SO4, Hgso4 CH3CH2Br HBr 1-equiv BH3/THF HBr 2-equiv CH3CH2CH2Br CH3Br H202/NaOH Br2 1-equiv NaOH NaNH2 Br2 2-equiv
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below. 2 equiv. NaNHz excess NaNH2 CH3Br H20, H2SO4, HgSO4 Na, NH3 (1) H2O2, NaOH, H2O NaBH4 HBr Br2 CH3CH2Br H2. Lindlar catalyst BH3/THF PBr3
In each reaction box, place the best reagent and conditions from the list below 1 LDA, THF 2) CH3CH2Br 3) 4) 5) 6) CrO3 NaBH4 NaCN CH3Br LiAlH4 Br2, H3Br2, NaOH CH3CN PBr3 KMnO4 Pyridine BH3, THF Br2, FeBr3 H2O
In each reaction box, place the best reagent and conditions from the list below 1) excess NaNH2 2) 3) 4) PBrs H2, Lindlar catalyst ВН+THF 2 equiv. NANH2 CH3Br Hо, НSO4, Hgso NaBH Na, NH3 () HаОг, NaOH, H>o HBr CH3CH2Br Br2
Item 16 Part 1-bromo 2 phenylethane Complete the scheme by dragging the appropriate label to its respective target. Reset Help Bra, Δ CH,CH4Br Bry, hw product of B HBr, OH Submit Request Answer Part 2-phenylethanol
In each reaction box, place the best reagent and conditions from the list below. You have the wrong reagent for the final step. An oxidizing agent is necessary to convert the boron functional group into an enol, which will tautomerize to the aldehyde. 1) Br2 DEDY 2) excess NaNH2, then H20 3) BH3/THF 2 equiv. NaNH2 H2, Lindlar catalyst bromocyclohexane HBr H20, H2SO4, HgSO4 NaBH4 CH3Br CH3CH2Br H2O2, NaOH, H20 SOCI2
Construct a three-step synthesis of trans-2-pentene from acetylene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. (Me = methyl, CH3; Et = ethyl, CH3CH2.) Question 20 of 20 sapling learning Construct a three-step synthesis of trans-2-pentene from acetylene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of...
In each reaction box, place the best reagent and conditions from the list below. Hint : The product is an epoxide, so work backwards to determine the intermediate and reagents. A peracid (such as mCPBA) is not available here, so what other method do you know to form epoxides? What reagent and starting material must be used to form this key intermediate? For the epoxide formation, consider the basicity and nucleophilicity of the base. Sapling Learning macmillan learning In each...
Question 29 of 34 Map In each reaction box, place the best reagent and conditions from the list below. 1) 2) 3) 4) Br2 mCPBA Br2, H20Pd, H2 H202, NaOH, H2O BHyTHF Br2, FeBr HBr NBS, ROOR , hv Previous ⓧ Give Up & View Solution D Check Answer、Next Exit Hint