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(b) Is UV spectroscopy a correct method to
distinguish between the Rectant and Product
Step by step
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- Need all IR and NMR assignments and the structure of the compoundPlease help with these two. Explain your reasoning and show calculation of degree of unsaturation. Also, draw the structure of each compound on IR/NMR spectrum.Writing down all the relevant resonant structures and that of the resonance hybrid, propose a mechanism that explains the reason why methyl benzoate is nitrated in the meta position.
- By giving the reagent and the visible result, differentiate each of the following pairsPart IIB Draw the structure of the synthesized product (do not include side or by products) from experiments performed in Chem 272L. How can IR spectroscopy be used to monitor the progress of each of the following reactions (if reaction went to completion and/or check the purity of the final product)? What absorptions would be observed in the IR spectrum? And if IR spectroscopy could not have been used, briefly explain why.Part IIDraw the structure of the synthesized product (do not include side or by products) from experiments performed in Chem 272L. How can IR spectroscopy be used to monitor the progress of each of the following reactions (if reaction went to completion and/or check the purity of the final product)? What absorptions would be observed in the IR spectrum? And if IR spectroscopy could not have been used, briefly explain why.
- How wouldyou use UV spectroscopy to distinguish between the reactant and the product ?explain with exampleHow can you distinguish a terminal alkyne and a nitrile using IR spectra? Explain using specific examples.IR spectroscopy does not distinguish very well betweenisomers I and J. Explain why. How could UV–vis spectroscopy be used to distinguish between them