2. Below are two other organic dyes that both produce a yellow color when dissolved. Which of the solvents used in this experiment (select one solvent for each dye) could be used to dissolve samples of each of these dyes (individual samples, not a mixture)? HN- Radiant Yellow Alizarine Yellow OH Na

Please answer ALL parts of the following related to organic chemistry.

Solvent #1 is a 50:50 mixture of hexane and ethyl acetate and solvent #2 is 25% hexane. Which solvent mixture is more polar: the 50:50 mixture or the 25:75 mixture? Explain briefly What would happen to the Rf of the spots in solvent #2 compared to solvent #1? Why?

Dispersion Dye, Acid Dye, and Direct Dye Which dye will be the most polar? The least polar? Explain.

Which tracking dye is used in SDS-PAGE? O bromothymol blue O bromophenol blue O coomassie blue O acridine dye

1015MSC Chemistry of Biological Systems II 2021 2. What kind of results do you expect to see when the following compounds are mixed together with the given test solution? Indicate positive or negative in the table below. (a) with 2,4-dinitrophenylhydrazine (b) with Benedict's reagent (c) with lodoform reagent CH3 (d) with Tollen's reagent

A student was trying to determine the identity of an unknown compound.  The melting point of the compound was 117-118oC. The student narrowed the possible compound down to the following:   Compound Melting Point Range acetanilide 113-115oC fluorene 114-116oC mandelic acid 120-122oC A second student, doing the same experiment as above, found that their melting point was 100-108oC.  What is wrong with the student’s melting point? Propose two reasons why the melting point could be incorrect. View keyboard shortcuts

These are IR spectra images that were taken in our lab (first is benzoic acid). Explain the IR peaks corresponding to the functional groups for both products.

3. 'H-NMR interpretation When dissolved in CDC13, phenacetin shows 6 signals. All of the peaks are sharp, except for the signal f not below. Draw the chemical structure of phenacetin, labeling each hydrogen with an alphabetical letter. Make a larger version of the chart below (half or full page), and complete it with the missing information. Explanation of splitting patter 8 (ppm) Letter # H (integration Splitting pattern value) 7.94 f 1 Broad singlet 7.36 e 6.80 d 3.98 с 2.09 b 1.38 a Extra Credit Question 4. Describe/predict how the 'H-NMR spectrum differs for acetaminophen.

The compounds you are separating are; Cholesterol/cholesterol acetate on a silica gel the solvent is ligroin:ether 9:1 Do not forget to find out if cholesterol and cholesterol acetate are colored compounds if not how will you visualize the separation of the products?