How could you separate lauric acid from alpha
WebHow could you separate lauric acid from Alpha-naphthol (see table 3.1) Expert Solution Want to see the full answer? Check out a sample Q&A here See Solution star_border … WebHow could you separate lauric acid from naphthol? Hence, in order to separate the two, the mixture can be reacted with an aqueous solution of sodium bicarbonate. This results in the deprotonation of lauric acid forming the sodium laurate salt which is soluble in water.
How could you separate lauric acid from alpha
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WebScience Chemistry Answer & Explanation Solved by verified expert Answered by herianmarie Question 1 Add cyclohexane. Since napthol is insoluble in cyclohexane, then you can filter out lauric acid Question 2 Use water to dissolve NaCl then filter out BaSO 4 Question 3 Submerge in hydroflouric acid. Web#5 To separate lauric acid from a-naphthol you can add cyclohexane to the mixture, and since a-naphthol is insoluble in cyclohexane, then you can decant the Build bright future …
WebHow could you separate lauric acid from a naphthol - Best of all, ... How could you separate lauric acid from alpha. The melting point for lauric acid is about 45 degrees while it is 121 degrees for naphthol. So, in a mixture repeated cycles of slow warming WebHow could you separate lauric acid from a Hence, in order to separate the two, the mixture can be reacted with an aqueous solution of sodium bicarbonate. This results in the deprotonation of lauric acid forming the sodium laurate salt which is soluble in water.
WebHow could you separate lauric acid from alpha Hence, in order to separate the two, the mixture can be reacted with an aqueous solution of sodium bicarbonate. This results in the deprotonation of lauric acid forming the sodium laurate salt which is soluble in water. Web27 de out. de 2016 · 1 Answer anor277 Oct 27, 2016 Well, α −napthol is failry involatile. Explanation: I just looked it up and the normal boiling point of α − napthol is over 250 ∘C. On the other hand, the normal boiling point of acetone is 56 ∘C. And thus a convenient means of separation would be distillation. Can you account for this difference in volatility?
WebHow would you separate laurie acid from alpha-naphtol? I know lauric acid is soluble in cyclohexane, but what would be done after this is added? Decanting then heating? Expert Answer 100% (2 ratings) As it is clearly known that lauric acid is insoluble in α-Napthol but it is fairly solubl … View the full answer Previous question Next question
on that score meaningWebHow could you separate lauric acid from a naphthol - The melting point for lauric acid is about 45 degrees while it is 121 degrees for naphthol. So, in a. ... How could you separate lauric acid from alpha #5 To separate lauric acid from a-naphthol you can add cyclohexane to the mixture, and since a-naphthol is insoluble in cyclohexane, ... on that senseWebHence, in order to separate the two, the mixture can be reacted with an aqueous solution of sodium bicarbonate. This results in the deprotonation of lauric acid forming the sodium laurate salt which is soluble in water. on that shelfWebTo seperate lauric acid from alpha-naphthol you can add cyclohexane to the mixture because alpha-naphthol is insoluble in cyclohexane while lauric acid is soluble in … on that scoreWebHow could you separate lauric acid from alpha. Hence, in order to separate the two, the mixture can be reacted with an aqueous solution of sodium bicarbonate. This results in … on that scheduleWebHow could you separate lauric acid from alpha-naphthol? This problem has been solved! You'll get a detailed solution from a subject matter expert that helps you learn core … on that same veinWebHow could you separate lauric acid from alpha. Hence, in order to separate the two, the mixture can be reacted with an aqueous solution of sodium bicarbonate. This results in the deprotonation of lauric acid forming the sodium laurate salt which is soluble in water. on that situation