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In each reaction box, place the best reagent and conditions from the list below. (A reagent may be used more than once.)
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In each reaction box, place the best reagent and conditions from the list below. (A reagent may be used more than once.)SO3, H2SO4acetyl chloride, pyridineH3O+, H2O, heatNaOH (room temp)HNO2, H2SO4NaNO3Br2, heatBr2, FeBr3CH3COOHHNO3, H2SO4H2, Pd or Fe/HCl or Sn/HCl
In each reaction box, place the best reagent and conditions from the list below. (A reagent may be used more than once.)
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...
In each reaction box, place the best reagent and conditions from the list below. Hint: Alkynes are slightly acidic hydrocarbons, a property important in extending the carbon chain. Notice that the product contains two more carbon atoms than the reactant. Note also that the product is a racemic vicinal diol with (R,R) and (S,S) configuration. Which of the reagents can produce a diol?
In each reaction box, place the best reagent and conditions from the list below. There is more than one possible route. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. CH3CHO, 2H2O CH2CH2CH2CHO, 2H2O CH3(CH2)2MgBr, H2O CH3MgBr, H2O CH3(CH2)2OH Mg CH3Br PCC HOCH2CH2OH, H+ H3O+
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. Only one of the reagents can react with the very unreactive cyclopentane. A radical intermediate is involved. PCC stands for pyridinium chlorochromate. It oxidizes a primary alcohol to an aldehyde or a secondary alcohol to a ketone.
In each reaction box, place the best reagent and conditions from the list below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. он 2. 3. он он
In each reaction box, place the best reagent and conditions from the list below. (Some reagents may be used more than once) In each reaction box, place the best reagent and conditions from the list below. (Some reagents may be used more than once.)
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...