Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Which of the compounds given below are the most probable identities of spots A, C, F, and J?  Explain your assignment of the identities of the spots. (Probably in terms if polarity of the compounds, Rf values, etc. anything that falls under paper chromatography).

6. Which molecule will have a larger R, on a SiO₂ TLC plate using 10% Ethyl acetate/hexane as eluent? Draw their structures and explain why. Benzoic acid or ethyl benzene?

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Q.1. Predict the relative intensity of the M, M+1, and M+2 peaks for a low resolution mass spectrum of a compound with molecular formula, C6H13Br. The natural abundances of the select isotopes are given below. 35 Cl: 75.8% 79Br: 50.5% 12C: 98.89% 37Cl: 24.2% (The ratio is almost 3:1) 81Br: 49.5% (The ratio is almost 1:1) 13C: 1.11%

Please Answer Part "B". Part "A" is attached for reference.

5. Properties and IMF: Chlorophyll a and Chlorophyll b are almost identical in structure, but they separated during TLC. Report the RFs you recorded for both molecules. What functional group(s) are different between them? Then explain these RF values by comparing the IMF present in each molecule to those present in the mobile or stationary phase and how this shaped their affinities for each phase. Use the terms RF, IMF, polar, nonpolar, affinity, mobile phase and stationary phase.

Please don't provide handwriting solution

Please help answering all parts of the following question...thank you! From the following sets of data, please propose a reasonable structure for the unknown organic compound. This molecule is entirely composed of C, H, and N only. Please show all of your work and feel free to write on the spectra any clues as to the structure.

In the TLC experiment you are give a mixture of benzoic acid C6H5COOH and 2-hydroxy benzoic acid C6H4 ( OH)COOH. Which will have a higher Rf value in a non polar solvent and why?

Let's say that you found the perfect eluent for separating benzoic acid and naphthalene on a silica gel TLC plate. Which compound would have the higher Rf value after you eluted the plate? (Hint: look up the structures for both of these compounds). O A. It cannot be determined with the given information. O B. Benzoic Acid O C. Neither. They would have the same Rf value. O D. Naphthalene