Yeah I suppose the question is somewhat badly phrased.xrtzx said:yeah i guess so........
Hence the assumption.nit said:No, bisulfate ion is a weak acid with pKa of 1.92 I think. Hence you can't assume it deprotonates fully, as it can't unless in the presence of base.
It says the beakers are labelled in order of collection AND that pure substances were collected. Since Methyl Propanoate has the second lowest BP it would have been collected in beaker 2.ishq said:We were taught:
The ester methy propanoate is prepared by refluxing a mixture of methanol and propanoic acid with conc sulfuric acid. After the reaction mixture has been cooled and poured into a large volume of water, the following procedure is used to purify the substance -
1. Stir the misture and separate into two layers. Discard the aqueous layer.
2. Add a small amount of sodium carbonate to the organic layer. Add water and shake the mixture. Allow the mixture to separate into two layers. Discard the aqueous layer.
3. Allow the organic layer to stand over a drying agent (anhydrous calcium chloride). Filter off the drying agent.
4. Distill the organic layer to obtain the PURE ester.
So, shouldnt it be Beaker 4?
Why does it say Beaker 2?
Ohh!!!!!Jumbo Cactuar said:It says the beakers are labelled in order of collection AND that pure substances were collected. Since Methyl Propanoate has the second lowest BP it would have been collected in beaker 2.