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The gasoline additive methyl t-butyl ether (MTBE) has been leaking into groundwater ever since its introduction in the. MTBE can be measured at parts per billion levels by solid-phase microextraction from groundwater to which 25 % (wt/vol) NaCl has been added (salting out, Problem 8-9). After microextraction, analytes are thermally desorbed from the fiber in the port of a gas chromatograph. The figure on the next page shows a reconstructed total ion chromatogram and selected ion monitoring of substances desorbed from the extraction fiber.

(a) What is the purpose of adding NaCl prior to extraction?

(b) What nominal mass is being observed in selected ion monitoring? Why are only three peaks observed?

(c) Here is a list of major ions above m/z50 in the mass spectra. The base (tallest) peak is marked by an asterisk. Given that MTBE and TAME have an intense peak at m/z,73 and there is no significant peak at m/z,73 for ETBE, suggest a structure for m/z,73. Suggest structures for all ions listed in the table.

Short Answer

Expert verified

(a) The inclusion of sodium chloride increases the percentage of organic compounds that will be transported to the fibre extraction process.

(b) Selective ion monitoring is used to measure ion abundance for m/z73, and only three chemicals are stated to have significant intensity in the extract at m/z73 .

(c) The structures shown below can be used as examples.

Step by step solution

01

Definition of NaCl, MTBE, TAME and ETBE

  • The chemical name for salt is sodium chloride. Sodium is an electrolyte that controls how much water your body holds. Nerve impulses and muscle contractions are also affected by sodium.
  • Dehydration, excessive sweating, and other causes of sodium loss are treated or prevented by sodium chloride.
  • The volatile organic compound (VOC) methyl tertiary butyl ether (MTBE) is extensively utilised as a gasoline additive.
  • MTBE is also known as 2-methoxy-2-methylpropane, methyl t-butyl ether, and methyl tert butyl ether.
  • TAME (tert-amyl methyl ether) is a kind of ether that is utilised as a fuel oxygenate.
  • Ethyl tert-butyl ether (ETBE) is a substitute for methyl tert-butyl ether (MTBE) that combines the blending capabilities of MTBE and the renewable nature of ethanol.
02

Determining the purpose of adding NaCl prior to extraction

(a)

  • It is necessary to explain why sodium chloride was added to the extraction earlier.
  • In water, sodium chloride lowers the solubility of non-polar molecules such as ethers. The inclusion of sodium chloride increases the percentage of organic compounds that will be transported to the fibre extraction process.
03

Determining the nominal mass being observed in selected ion monitoring and why only three peaks are observed

(b)

  • The nominal mass seen in selected ion monitoring must be provided, as well as the explanation for the detection of three peaks.
  • The nominal mass seen in chosen ion monitoring, as well as the explanation for the detection of three peaks, must be provided.
  • Selective ion monitoring is used to measure ion abundance for m/z 73, and only three chemicals are stated to have significant intensity in the extract at m/z 73.
04

Determining the structures for all ions listed in the table

(c)

For the values in the table, the peaks must be suggested.

To make suggestions for the peaks for the values in the table

m/z 73 Base peaks for MTBE and TAME have been discovered. This mass relates to M-15 (loss of mass) in the case of MTBE CH3TAME's mass, on the other hand, relates to M-29 (a reduction in C2H5) . The loss of the ethyl group in TAME, which is connected to carbon, suggests that the methyl group lost in MTBE is also tied to carbon, rather than oxygen.

If the methyl group related to oxygen was easily lost from MTBE and TAME, the ethyl group linked to oxygen should be easily lost from ETBE. There isn't a prominent crest at M-29( m/z 73 in ETBE.

The structures shown below can be used as examples.

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Most popular questions from this chapter

(a) What types of solutes are typically separated with a poly(dimethylsiloxane)-coated open tubular column?

(b) What types of solutes are typically separated with a poly(ethylene glycol)-coated open tubular column?

(c) What types of solutes are typically separated with a porous-layer open tubular column?

(a) When would you use split, split less, or on-column injection in gas chromatography?

(b) Explain how solvent trapping and cold trapping work in split less injection.

Here is a student procedure to measure nicotine in urine. A 1.00-mL sample of biological fluid was placed in a 12-mL vial containing 0.7gNa2CO3powder. After 5.00μ²µof the internal standard 5 -aminoquinoline were injected, the vial was capped with a Teflon coated silicone rubber septum. The vial was heated to 80°cfor 20 min and then a solid-phase microextraction needle was passed through the septum and left in the headspace for 5.00min. The fiber was retracted and inserted into a gas chromatograph. Volatile substances were desorbed from the fiber at 250°cfor 9.5min in the injection port while the column was at 60°c. The column temperature was then raised to 250°cat 25°c/minand eluate was monitored by electron ionization mass spectrometry with selected ion monitoring at m/z 84 for nicotine and m / z 144 for internal standard. Calibration data from replicate standard mixtures taken through the same procedure are given in the table.

(a) Why was the vial heated to 80°cbefore and during extraction?

(b) Why was the chromatography column kept at 60°Cduring thermal desorption of the extraction fiber?

(c) Suggest a structure for m / z 84 from nicotine. What is the m / z, 144 ion from the internal standard, 5 -aminoquinoline?

(d) Urine from an adult female nonsmoker had an area ratio m / z .84 / 144=0.51 and 0.53 in replicate determinations. Urine from a nonsmoking girl whose parents are heavy smokers had an area ratio 1.18 and 1.32.

Find the nicotine concentration (μ²µ/L)and its standard uncertainty in the urine of each person.

The graph shows van Deemter curves for n-nonane at . in the 3.0-m-long microfabricated column in Box 24-2 with a -thick stationary phase.

van Deemter curves. [Data from G. Lambertus, A. Elstro, K. Sensenig, J. Potkay, M. Agah, S. Scheuening, K. Wise, F. Dorman, and R. Sacks, "Design, Fabrication, and Evaluation of Microfabricated Columns for Gas Chromatography," Anal. Chem. 2004, 76, 2629.]

(a) Why would air be chosen as the carrier gas? What is the danger of using

air as carrier gas?

(b) Measure the optimum velocity and plate height for air and for carrier

gases.

(c) How many plates are there in the 3 -m-long column for each carrier gas at

optimum flow rate?

(d) How long does unretained gas take to travel through the column at

optimum velocity for each carrier gas?

(e) If stationary phase is sufficiently thin with respect to column diameter, which of the two mass transfer terms (23-40 or 23-41) becomes negligible?

Why?

(f) Why is the loss of column efficiency at high flow rates less severe for

than for air carrier gas?

(a) When a solution containing234mg of pentanol (FM 88.15) and237mg of 2,3 -dimethyl-2-butanol (FM 102.17) in10.0ml was separated, relative peak areas were pentanol: 2,3 -dimethyl-2-butanol = 0.913 : 1.00. Considering pentanol to be the internal standard, find the response factor for 2,3 -dimethyl-2-butanol.

(b) Use Equation 24-8 to find the areas for pentanol and 2,3 -dimethyl-2-butanol in Figure 24-8.

(c) The concentration of pentanol internal standard in the unknown solution was93.7mM . What was the concentration of 2,3 -dimethyl2-butanol?

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