You synthesized 1-chlorobutan-2-ol in lab, and the next step is to confirm the identity of your product through characterization. Unfortunately, the IR broke down the day you successfully isolated your product. You tried the NMR, but found that it was fully booked for the whole week. To confirm the identity of your product, your instructor recommended that you perform at least three classical qualitative tests. What tests would you choose and how would you expect your product to react to these tests?

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Q: 8.874 -8.869 8.864 -8.433 L8.430 8.427 8.424 L8.412 8.409 8.406 -8.403 -8.382 -8.379 8.375 -8.363…

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Q: Using the provided 1H NMR spectra of N-(4-Ethoxy-2-nitrophenyl)acetamide, please label the protons,…

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Q: P

A:

Q: c. Describe the coupling pattern (i.e. doublet, triplet, doublet of doublets, etc.) for the peak at…

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Q: i. 4-methyl-2-pentanone 100 - 80 60 40 20 10 20 30 40 50 60 70 80 90 100 m/z Identify the structure…

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Q: 13)A student ran the reaction shown below. What would you expect the structure of the product to be?…

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Q: Sketch an H-NMR spectra of the final product, p-nitroacetanilide

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Q: 4. Assign a structure that is consistent with each of the following 'H NMR spectra. C. C„H1„O…

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Q: 5000 -3000 2000 80 7.5 6.5 6.0 25 어 102

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Q: Evaluate the NMR provided. To what does the peak at around 4 ppm belong? What does this suggest…

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NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.