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A bonded stationary phase for the separation of optical isomers has the structure

To resolve the enantiomers of amines, alcohols, or thiols, the compounds are first derivatized with a nitroaromatic group that increases their interaction with the bonded phase and makes them observable with a spectrophotometric detector.

When the mixture is eluted with 20 vol% 2-propanol in hexane, the (R)-enantiomer is eluted before the (S)-enantiomer, with the following chromatographic parameters:

Resolution=Δtrwav=7.7

Relative retention(α)=4.53

k for (R)-isomer =1.35

tm=1.00min

wherewavis the average width of the two Gaussian peaks at their base.

(a) Findt1,t2andwawith units of minutes.

(b) The width of a peak at half-height isrole="math" localid="1663582749865" w1/2(Figure 23-9). If the plate number for cach peak is the same, findw1/2for each peak.

(c) The area of a Gaussian peak is1.064×peakheight×w1/2. Given that the areas under the two bands should be equal, find the relative peak heights(heightR//heightS).

Short Answer

Expert verified

a) The values aret1=2.35min,t2=7.11min,wav=0.619min.

b)The half-width of peak 1 is 0.181min.

The half-width of peak 2 is 0.548min .

c) The relative heights of two peaks is 3.0.

Step by step solution

01

Definition of compound

A compound is a substance made up of two or more chemical components that have been chemically bonded together. Covalent bonds and ionic bonds are two typical forms of bonds that hold components in a compound together. In any compound, the components are always present in set ratios.

02

Step 2: Values of t1t2,wav 

a)

To find the retention time of R-isomer,

tmis given as 1.00min.

Retention factor (k) is given as 1.35.

The t1retention time may be computed by substituting the aforementioned numbers in the retention factor equation, as shown below.

k=t1-tmtm=t1-1.001.001.35=t1-1.001.00t1=1.35+1.00t1=2.35min

The R-isomer retention time is computed as 2.35 min.

The retention period of the S -isomer may be calculated using the equation for relative retention.

4.53 is the relative retentionα.

The retention period for R-isomer is2.35mint1.

Relative retentionα=ts¢ts1'

4.53=t2-1.00t1-1.00=t2-1.002.35-1.00t2=4.531.351.00=6.11+1.00

The retention time of S-isomer is 7.11min.

To find the average width, divide the whole length by the total width.

The resolution and difference in retention time of the two isomers may be used to compute the average width.

4.77min is the difference in retention time.

In the problem statement, the solution is provided as 7.7.

As demonstrated below, the average width may be computed.

Resolution=tywas7.7=4.77wavwav=4.777.7=0.619min

The average width at the base is calculated as 0.619min.

03

Step 3:Values of w1/2 for each peak

b)

The equation below can be used to compute the plate number.

N=5.54trw1n2

If the plate number is constant, it may deduce that retention time is proportional to half-width.

Hence,

w1npeak1w12peak2=t1t2=2.357.11=0.330

The average width at the base was calculated as0.62min.

It is known that for each peak, the width (w) is equal to4σ and half-widthw1n is2.35σ.

From the above two equations,w was found as1.70w1/2.

The average base width is 0.62min.

wav=12w1+w2=121.70w1/2peak1+1.70w1/2peak2

It is known that

w1/2(peak1)=0.330(w1/2(peak2)

Substituting this into the basic equation's average width

wav=121.700.330w1/2peak2+1.70w1/2peak2=120.561w1/2peak2+1.70w1/2peak21.24=2.26w1/2peak2w1/2peak2=1.242.261=0.548min

The half-width of peak 2 is 0.548min.

As illustrated below, the half-width of peakmay be determined from this.

w1/2peak1=0.330(w1/2peak2=0.330×0.548=0.18084min=0.181min

In the provided chromatogram, the half-width of both peaks was calculated.

04

Step 4: Relative peak height

c)

The half-width of peak 1 is 0.181min.

The half-width of peak 2 is 0.584min.

The regions under both peaks are equal, according to the problem statement.

HeightR×wR=HeightS×wSHeightRHeright=wSwR=0.5480.181=3.0

The relative heights of the two peaks is calculated as 3.0.

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Most popular questions from this chapter

In monolithic columns60 the stationary phase is a single porous piece of silica or polymer filling the entire column and synthesized within the column from liquid precursors. Monolithic columns offer similar plate height to HPLC particles, but with less resistance to flow. Therefore, faster flow or longer columns can be used. The figure shows separation of isotopic molecules on a long monolithic column. Packed columns have too much resistance to flow to be made so long.

Separation of isotopic molecules on a 440-cm-long monolithic C18-silica column eluted withCH3CN/H2O(30: 70 vol/vol) at 308C. [Data from K. Miyamoto, T. Hara, H. Kobayashi, H. Morisaka, D. Tokuda, K. Horie, K. Koduki, S. Makino, O. Nuñez, C. Yang, T. Kawabe, T. Ikegami, H. Takubo, Y. Ishihama, and N. Tanaka, “High-Efficiency Liquid Chromatographic Separation Utilizing Long Monolithic Silica Capillary Columns,” Anal. Chem. 2008, 80, 8741.]

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