In each reaction box, place the best reagent and conditions from the list below.
First, acetic acid is reduced to ethyl alcohol with lithium
aluminum hydride followed by water. The ethanol is oxidized to
acetaldehyde by PCC (pyridinium chlorochromate). Then acetaldehyde
reacts with methyl amount in presence of catalytic amount of acid
to form the end product.
Note: PCC is a mild oxidising agent which oxidizes alcohol to
aldehyde. Further oxidation to acid does not occur.
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. 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. 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. 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. 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. You are correct that the third step is a reduction of 2-pentyne. But H2 with a platinum catalyst will reduce it to pentane, while you need an alkene for the next step. NaNH H3C OH HO 2) CH3CH2Br CEC H3C CH3. H3C H2, Pt HO 4) KMno 4, NaOH, H20, cold BH3...
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. 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. Incorrect. A complex mixture of regioisomers would be obtained in the final step if Friedel-crafts acylation were performed as the first step.
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.