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Heptane, decane, and an unknown had adjusted retention times of 12.6min(heptane),22.9min(decane), and20.0min(unknown). The retention indexes for heptane and decane are 700 and 1000 , respectively. Find the retention index for the unknown.

Short Answer

Expert verified

The unknown has a retention index of 932.

Step by step solution

01

Definition of retention index

  • The retention index of a sample component is a number calculated by interpolation (usually logarithmic).
  • And relating the sample component's adjusted retention volume (time) or retention factor to the adjusted retention volumes (times) of two standards eluted before and after the sample component's peak.
02

Determine the retention index for the unknown.  It is necessary to compute the unknown's retention index.

It is necessary to compute the unknown's retention index.

Retention index of Kovats:

For linear alkanes, the retention index, I, equals 100 times the number of carbon atoms.

I=800 for an Octane molecule.

For a Nonane molecule,l=900

Using the calculation, the retention index of a compound eluted between Octane and Nonane will be between 800 and 900,

l=100n+N-nlogtr'(unknown)-logtr'nlogtr'N-logtr'nThenumberofcarbonatomsinasmalleralkaneisequalton.Nrepresentsthenumberofcarbonatomsinabiggeralkane.trn=smalleralkaneretentiontimehasbeenalteredt'rN=Alkaneretentiontimehasbeenalteredforlargeralkanes.Calculatetheunknown'sretentionindex.Given,Heptaneretentiontimewasadjustedto12.6minutes.Decaneretentiontimehasbeenadjustedto22minutes.Unknownretentiontimewasadjustedto20.0minutes.Heptaneretentionindex=700Decane'sretentionindexis1000.Theunknown'sretentionindexisdeterminedas,l=100n+N-nlogtr'unknown-logtr'nlogtr'N-logtr'nl=1007+(10-7)log(20.0)-log(12.6)log(22.9)-log(12.6)l=1007+(3)1.3010-1.10031.3598-1.1003l=1007+(3)0.20070.2595l=932Theunknown'sretentionindexis932.Theunknown'sretentionindexwascalculatedanddeterminedtobe932.

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Most popular questions from this chapter

The antitumor drug gimatecan is available as nearly pure (S)-enantiomer. Neither pure (R)-enantiomer nor a racemic (equal) mixture of the two enantiomers is available. To measure small quantities of (R)-enantiomer in nearly pure (S)-gimatecan, a preparation was subjected to normal-phase chromatography on each of the enantiomers of a commercial, chiral stationary phase designated (S,S)- and (R,R)-DACH-DNB. Chromatography on the (R,R)-stationary phase gave a slightly asymmetric peak at tr 5 6.10 min with retention factor k 5 1.22. Chromatography on the (S,S)- stationary phase gave a slightly asymmetric peak at tr 5 6.96 min with k 5 1.50. With the (S,S) stationary phase, a small peak with 0.03% of the area of the main peak was observed at 6.10 min.

Chromatography of gimatecan on each enantiomer of a chiral stationary phase. Lower traces have enlarged vertical scale. [Data from E. Badaloni, W. Cabri, A. Ciogli, R. Deias, F. Gasparrini, F. Giorgi, A. Vigevani, and C. Villani, 鈥淐ombination of HPLC 鈥業nverted Chirality Columns Approach鈥 and MS/MS Detection for Extreme Enantiomeric Excess Determination Even in Absence of Reference Samples.鈥 Anal. Chem. 2007, 79, 6013.]

(a) Explain the appearance of the upper chromatograms. Dashed lines are position markers, not part of the chromatogram. What Problems 709 would the chromatogram of pure (R)-gimatecan look like on the same two stationary phases?

(b) Explain the appearance of the two lower chromatograms and why it can be concluded that the gimatecan contained 0.03% of the (R)-enantiomer. Why is the (R)-enantiomer not observed with the (R,R)-stationary phase?

(c) Find the relative retention (a) for the two enantiomers on the (S,S)-stationary phase.

(d) The column provides N 5 6 800 plates. What would be the resolution between the two equal peaks in a racemic (equal) mixture of (R)- and (S)-gimatecan? If the peaks were symmetric, does this resolution provide baseline separation in which signal returns to baseline before the next peak begins?

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.

This problem reviews concepts from Chapter 23. An unretained solute passes through a chromatography column in 3.7 min and analyte requires 8.4 min.

(a) Find the adjusted retention time and retention factor for the analyte.

(b) Find the phase ratio b for a 0.32-mm-diameter column with a 1.0-mm-thick film of stationary phase.

(c) Find the partition coefficient for the analyte.

(d) Determine the retention time on a similar length of 0.32-mm diameter column with a 0.5-mm-thick film of the same stationary phase at the same temperature.

Why is split less injection used with purge and trap sample preparation?

When 1.06 mmol of 1-pentanol and 1.53 mmol of 1-hexanol were separated by gas chromatography, they gave peak areas of 922 and 1570 units, respectively. When 0.57 mmol of pentanol was added to an unknown containing hexanol, the peak areas were 843:816 (pentanol:hexanol). How much hexanol did the unknown contain?

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