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. In each reaction box, place the bes...
In each reaction box, place the best reagent and conditions from the list below. n each reaction box...
In each reaction box, place the best reagent and conditions from
the list below.
n each reaction box, place the best reagent and conditions from the list below. The third step is correct, but the others are not. PCC oxidizes an alcohol to a carbonyl group. Which reagents will convert an alkene to a hydroxyl group, and with the necessary regioselectivity? 2) NaBH in EtOH 3) PCC in CH2Cl2 PhCO3H in CH2012 CH30Na in CH3OH B2H6 in THF in CH2Cl2...
in each reaction box place the best reagent and conditions from the list below. aldehyde
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. Your reagent for the third step is incorrect. In this step an alcohol is converted to an aldehyde.
in each reaction box place the best reagent and conditions from the list below cyclohexene
In each reaction box, place the best reagent and conditions from
the list below.
Hint:PCC is pyridinium chlorochromate. Ph represents a phenyl
group, C6H5. Et represents an ethyl group, CH3CH2
1-methylcyclohexene + (?) + (?) ----> 2-methoxyphenol (aka
Guaiacol)
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the bes...
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.
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. In each reaction box, place the best reagent and conditions from the list below. Your reagent for the first step is incorrect. This reaction involved a double elimination of HBr to form an alkyne. Which reagent is a strong base capable of carrying out this reaction ?
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. 1) H3 2) 3) Br2 PBr3 KMnO4 NaOH Br2, FeBr3HBr CrO3. H2S04, H2O HBr, h H202, NaOH, H20 CH30 NBS, ROOR, hv PCC
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. PCC Brz, H20 HBr, hv PBr3 CH3CH2CI, AICI: KMnO4 NBS, ROOR, hy Brz, FeBrz HCOO- HBr CH3CI, AICI: HOC Brz CrO2, H2SO4, H20
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the bes...
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. CH2CCH3 CH3CH2CH2CI, AICI3 CH3COO BH3 THF CrO3, H2SO4 HBr HCEC H202, NaOH, H20 Bra, FeBr3 NBS, ROOR, hv CH3Cl, AICI3 Br2 Brz, H20
FIND REAGENTS? In each reaction box, place the best reagent and conditions from the list below....
FIND REAGENTS?
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.
In each reaction box, place the best reagent and conditions from the list below. A reagent...
In each reaction box, place the best reagent and conditions from the list below. A reagent may be used more than once.) Alkylating with ethyl bromide in steps 2 and 4 will lengthen the alkyne by two carbons at both ends but will not introduce the primary alcohol functional group.
In each reaction box, place the best reagent and conditions from
the list below.
n each reaction box, place the best reagent and conditions from the list below. The third step is correct, but the others are not. PCC oxidizes an alcohol to a carbonyl group. Which reagents will convert an alkene to a hydroxyl group, and with the necessary regioselectivity? 2) NaBH in EtOH 3) PCC in CH2Cl2 PhCO3H in CH2012 CH30Na in CH3OH B2H6 in THF in CH2Cl2...
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. Your reagent for the third step is incorrect. In this step an alcohol is converted to an aldehyde.
In each reaction box, place the best reagent and conditions from
the list below.
Hint:PCC is pyridinium chlorochromate. Ph represents a phenyl
group, C6H5. Et represents an ethyl group, CH3CH2
1-methylcyclohexene + (?) + (?) ----> 2-methoxyphenol (aka
Guaiacol)
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.
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. In each reaction box, place the best reagent and conditions from the list below. Your reagent for the first step is incorrect. This reaction involved a double elimination of HBr to form an alkyne. Which reagent is a strong base capable of carrying out this reaction ?
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. 1) H3 2) 3) Br2 PBr3 KMnO4 NaOH Br2, FeBr3HBr CrO3. H2S04, H2O HBr, h H202, NaOH, H20 CH30 NBS, ROOR, hv PCC
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. PCC Brz, H20 HBr, hv PBr3 CH3CH2CI, AICI: KMnO4 NBS, ROOR, hy Brz, FeBrz HCOO- HBr CH3CI, AICI: HOC Brz CrO2, H2SO4, H20
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. CH2CCH3 CH3CH2CH2CI, AICI3 CH3COO BH3 THF CrO3, H2SO4 HBr HCEC H202, NaOH, H20 Bra, FeBr3 NBS, ROOR, hv CH3Cl, AICI3 Br2 Brz, H20
FIND REAGENTS?
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.
In each reaction box, place the best reagent and conditions from the list below. A reagent may be used more than once.) Alkylating with ethyl bromide in steps 2 and 4 will lengthen the alkyne by two carbons at both ends but will not introduce the primary alcohol functional group.
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