In each reaction box, place the best reagent and conditions from
the list below.
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In each reaction box, place the best reagent and conditions from
the list below.
O OY...
In each reaction box, place the best reagent and conditions from the list below. OOY NaBHA CH3CH2Br 2 equiv. NaNH2 Brz...
In each reaction box, place the best reagent and conditions from the list below. OOY NaBHA CH3CH2Br 2 equiv. NaNH2 Brz BHY/THF H2O2. NaOH, H20 SOCI HBR H2. Lindlar catalyst H20, H2SO4, HgSO4 bromocyclohexane excess NaNH2, then H2O CH3Br
In each reaction box, place the best reagent and conditions from the list below. In each...
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. You have...
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
In each reaction box, place the best reagent and conditions from the list below. mu have...
In each reaction box, place the best reagent and conditions from the list below. mu have the right idea for generating an alkyne in the first two steps. Remember that a primary alkyne also reacts with NaNH2 to form the alkylide ion, so with only two equivalents of NaNH2 you will d up with a mixture of some alkylide anion, some unreacted vinyl bromide and probably some unreacted vicinal dibromide. Br2 O 2 equiv. NaNH2 OY BH3/THF 3) 4) H2O2,...
In each reaction box, place the best reagent and conditions from the list below. CH3 HBr...
In each reaction box, place the best reagent and conditions from the list below. CH3 HBr CH3Br Br2 H2, Lindlar catalyst bromocyclohexane BH3 THF H202, NaOH, H20 H20, H2SO4 excess NaNH2 CH3CH2Br SOC
In each reaction box, place the best reagent and Conditions from the list below. H C...
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...
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. CH3 BH3 THF H20, H2SO4 excess NaNH2 HBr SOCI2 CH3CH2Br H2, Lindlar catalyst H202, NaoH, H20 Br2 bromocyclohexane CH3Br
In each reaction box, place the best reagent and conditions from the list below. CH3 2)...
In each reaction box, place the best reagent and conditions from the list below. CH3 2) 3) H2, Lindlar catalyst H2O, H2SO4 CH3CH2Br Br2 bromocyclohexane BH3/THF SOCl2 excess NaNH2 HBr CH3Br H2O2, NaOH, H2O
In each reaction box, place the best reagent and conditions from the list below 1) 2)...
In each reaction box, place the best reagent and conditions from the list below 1) 2) 3) 4) HBr PВrg Вн/THF excess NaNH2 H20, H2SO4, HgSO4 NaBH4 CH3Br H2, Lindlar catalyst H2O2, NAOH, H20 СH-CH2Br Br2 Na, NH3 () 2 equiv. NaNH2
Please include the mechanism In each reaction box, place the best reagent and conditions from the...
Please include the mechanism
In each reaction box, place the best reagent and conditions from the list below. CEOY bromocyclohexane H2O, NaOH, H,O H, Lindlar catalyst excess NaNH2, then H2O 2 equiv. NaNH2 CH3Br SOCI H20, H2SO4, HgSO4 CH3CH2B1 NaBH4 BHYTHF НВК Br2
In each reaction box, place the best reagent and conditions from the list below. OOY NaBHA CH3CH2Br 2 equiv. NaNH2 Brz BHY/THF H2O2. NaOH, H20 SOCI HBR H2. Lindlar catalyst H20, H2SO4, HgSO4 bromocyclohexane excess NaNH2, then H2O CH3Br
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. 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
In each reaction box, place the best reagent and conditions from the list below. mu have the right idea for generating an alkyne in the first two steps. Remember that a primary alkyne also reacts with NaNH2 to form the alkylide ion, so with only two equivalents of NaNH2 you will d up with a mixture of some alkylide anion, some unreacted vinyl bromide and probably some unreacted vicinal dibromide. Br2 O 2 equiv. NaNH2 OY BH3/THF 3) 4) H2O2,...
In each reaction box, place the best reagent and conditions from the list below. CH3 HBr CH3Br Br2 H2, Lindlar catalyst bromocyclohexane BH3 THF H202, NaOH, H20 H20, H2SO4 excess NaNH2 CH3CH2Br SOC
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. CH3 BH3 THF H20, H2SO4 excess NaNH2 HBr SOCI2 CH3CH2Br H2, Lindlar catalyst H202, NaoH, H20 Br2 bromocyclohexane CH3Br
In each reaction box, place the best reagent and conditions from the list below. CH3 2) 3) H2, Lindlar catalyst H2O, H2SO4 CH3CH2Br Br2 bromocyclohexane BH3/THF SOCl2 excess NaNH2 HBr CH3Br H2O2, NaOH, H2O
In each reaction box, place the best reagent and conditions from the list below 1) 2) 3) 4) HBr PВrg Вн/THF excess NaNH2 H20, H2SO4, HgSO4 NaBH4 CH3Br H2, Lindlar catalyst H2O2, NAOH, H20 СH-CH2Br Br2 Na, NH3 () 2 equiv. NaNH2
Please include the mechanism
In each reaction box, place the best reagent and conditions from the list below. CEOY bromocyclohexane H2O, NaOH, H,O H, Lindlar catalyst excess NaNH2, then H2O 2 equiv. NaNH2 CH3Br SOCI H20, H2SO4, HgSO4 CH3CH2B1 NaBH4 BHYTHF НВК Br2
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