• Also, identify anything that would stop you from making a unique, positive identification of butan- 2-one. Did the spectra you picked match your initial description? 3. explain why the spectra belongs with the chemical in the bottle.

3 2 1.50 (ppm) 1.00 10 00 5 3 N o (ppm)

1.50 8.1 8 7.9 7.8 7.7 7.6 7.5 7.4 (ppm) 1.00 1.00 10.50 10 8 6 5 3 N (ppm) (2pts) Compound 1: methyl butanoate Provide an identification scheme for methyl butanoate • Include a brief outline of how you would identify methyl butanoate • Insert a drawing of methyl butanoate as well with reasonable peak shifts and descriptions. Also, identify anything that would stop you from making a unique, positive identification of any of the chemicals.

At 2.3 ppm a CH2 attached to the carbonyl has 1 Brief outline to identify methyl butanoate Additional information used to ID methyl butanoate Things that would prevent the identification of methyl butanoate Explain why the spectra belongs with methyl butanoate. Be specific. Strong oxidizing acids may cause a reaction that is sufficiently exothermic to ignite the reaction products. The effect of selective esterase inhibitors showed that both groups can be characterized as carboxylesterase, because © 2003-2020 Chegg Inc. All rights reserved. (2pts) Compound 1: methyl butanoate Provide an identification scheme for methyl butanoate • Include a brief outline of how you would identify methyl butanoate • Insert a drawing of methyl butanoate as well with reasonable peak shifts and descriptions.

6.00 2 o (ppm) 1.00 1.00 10 9 OD 5 3 N 8 (ppm) الي 1.50 2.5 2.3 2.1 21.8 1.6 5 (ppm) 1.4 1.2 1.00 10 7 5 5 (ppm) 2

3 2 1.50 8 (ppm) 1.00 10 8 7 6 5 2 (ppm) Did the spectra you picked match your initial description? The hydrolysis of methyl butyrate and 4-nitrophenyl butyrate by plasma, liver, lung, heart, diaphragm, cerebrum, kidney and duodenum of rat have been compared. The results showed that the two substrates were hydrolysed preferentially by two different groups of the enzyme. 1.00 3.00 8.1 8 7.9 7.8 7.7 7.6 7.5 o (ppm) 2.00 10 9 8 6 5 3 2 2 5 (ppm) Did the spectra you picked match your initial description? Be specific You may also use your knowledge of other tests or chemistries to help ID these chemicals.
Did the spectra you picked match your initial description 2 Brief outline to identify benzaldehyde Additional information used to ID benzaldehyde Things that would prevent the identification of benzaldehyde Explain why the spectra belongs with benzaldehyde.

1.50 3 2 (ppm) 1.00 1.00 10 8 2 5 (ppm) Flammable hydrogen is generated by mixing with alkali metals and hydrides (NTP, 1992).

3 Brief outline to identify 1-chlorobutane Additional information used to ID 1-chlorobutane Things that would prevent the identification of 1-chlorobutane Explain why the spectra belongs with 1-chlorobutane. Additional information used to ID 1-chloro-2-methylpropane Things that would prevent the identification of 1-chloro-2-methylpropane Explain why the spectra belongs with 1-chloro-2-methylpropane.

Did the spectra you picked match your initial description? For each of the following 7 chemicals: • methyl butanoate benzaldehyde • 1-chlorobutane 1-chloro-2-methylpropane butan-2-one • propan-2-ol propanal you will do the following: 1. provide an identification scheme. © 2003-2020 Chegg Inc. All rights reserved. Based on your knowledge of how NMR spectroscopy probes molecules, author a brief outline of how you would identify each of the seven chemicals above Insert a drawing of the chemical as well with reasonable peak shifts and descriptions. 1.00 2 (ppm) 0.67 0.67 10 9 00 7 OD 5 2 (ppm) Heat is also generated by interaction with basic or caustic solutions.

Normal: BIILU X2 | X? 7 Brief outline to identify propanal Additional information used to ID propanal Things that would prevent the identification of propanal Explain why the spectra belongs with propanal. Did the spectra you picked match your initial description? When inserting the image, resize the image and use the image editing tools (select image and click on red button that appears) to crop and rotate the image as needed • You may also use your knowledge of other tests or chemistries to help ID butan-2-one. 3.00 3 2.8 2.5 2.2 2 1.8 1.5 1.2 1 0.8 (ppm) 1.00 2.00 10 8 2 5 (ppm) 2. download the spectra (A-J on the NMR Spectra tile), analyze each, and select the letter ID of the spectra. Be enerifi waliban in carting the image .than Mac and the image dining tale leelast
REPORT SUMMARY 2pts) Compound 1: methyl butanoate Provide an identification scheme for methyl butanoate • Include a brief outline of how you would identify methyl butanoate • Insert a drawing of methyl butanoate as well with reasonable peak shifts and descriptions. Be Specific.

For each of the following 7 chemicals: • methyl butanoate benzaldehyde • 1-chlorobutane 1-chloro-2-methylpropane butan-2-one • propan-2-ol propanal you will do the following: 1. provide an identification scheme.

| E1319 fx180 BEI 991 illi Brief outline to identify methyl butanoate Drawing of methyl butanoate Expected peak shifts and descriptions Additional information used to ID methyl butanoate Things that would prevent the identification of methyl butanoate • Also, identify anything that would stop you from making a unique, positive identification of methyl butanoate. 6 Brief outline to identify propan-2-ol Additional information used to ID propan-2-ol Things that would prevent the identification of propan-2-ol Explain why the spectra belongs with propan-2-ol.

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