Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

use figure 25-17to suggest which type of liquid chromatography you could use to separate compounds in each of the following categories.

(a)Molecular mass <2000,soluble in octane

(b) Molecular mass <2000 ,soluble in methanol-water mixtures

(c) Molecular mass <2000 ,weak acid

(d)Molecular mass<2000 ,soluble highly polar

(e) Molecular mass <2000 ,ionic

(f)Molecular mass<2000,soluble in water in nonionic various

(g) Molecular mass<2000,soluble in water in water, variety of changes

(h) Molecular mass<2000,soluble in tetrahydrofuran

Short Answer

Expert verified

which type of liquid chromatography you could use to separate compounds.

a)We would use normal-phase chromatography

b)We would use bonded reverse-phase chromatography

c)We would use bonded reverse-phase chromatography.

d)We would use hydrophilic interaction chromatography

e)We would use ion-exchange or ion

f)We would use molecular-exclusion

g)We would use ion-exchange with wide pore stationary phase chromatography

h)We would use molecular-exclusion chromatography.

Step by step solution

01

Molecular mass

Figure 25-17is used to solve this.

If the analyte's molecular mass is less than 2 000 , we use the upper part of the figure. We use the lower part if the molecular mass is greater than 2 000 .Table 25-4can also be used to determine the polarity.

a)Molecular mass <2000,soluble in octane.

We would use normal-phase chromatography to separate compound that has molecular mass below 2 000 and it is soluble in octane.

b)Molecular mass <2000,soluble in methanol-water mixtures

We would use bonded reverse-phase chromatography to separate compound with molecular mass below 2 000 and it is soluble in methanol-water mixtures.

c)Molecular mass <2000,weak acid

We would use bonded reverse-phase chromatography with buffered mobile phase to separate compound with molecular mass below 2 000 and it is weak acid.

02

soluble highly polar

d)Molecular mass <2000,soluble highly polar

We would use hydrophilic interaction chromatography to separate compound with molecular mass below 2 000 and it is highly polar.

e)Molecular mass <2000,ionic

We would use ion-exchange or ion chromatography to separate compound with molecular mass below 2 000 and it is ionic.

f)Molecular mass <2000,soluble in water in nonionic various

We would use molecular-exclusion chromatography to separate compound with molecular mass greater than 2 000 and it is soluble in water, nonionic, various sized solutes.

g)Molecular mass >2000,soluble in water in water, variety of changes

We would use ion-exchange with wide pore stationary phase chromatography to separate compound with molecular mass greater than 2000 and it is soluble in water, variety of charges.

h)Molecular mass >2000,soluble in tetrahydrofuran

We would use molecular-exclusion chromatography to separate compound with molecular mass greater than 2 000 and it is soluble in tetrahydrofuran.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

The figure shows the separation of two enantiomers on a chiral stationary phase.


Sepation of enantiomers of Ritalin by HPLC with a chiral stationary phase.[Data from R.Bakhitar,L.Ramos,and F.L.S.Tse, “Quantification of methlylphenidate in plasma using chiral Liquid-chromatography/Tandem mass spectrometry: Application to Toxicokinetric studies,”Anal Chim Acta 2002,469,261.]

(a)From trandw1/2 find N for each peak.

(b) Fromtrandw1/2find the resolution.

(c)Giventm=1.62min, use Equation23-23with the average N to predict the resolution.

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.]

(a) Unretained thiourea is eluted in 41.7 min. Find the linear velocity ux (mm/s).

(b) Find the retention factor k forC6D6

(c) Find the plate number N and plate height forC6D6

(d) Assuming that the peak widths forC6H5Dand C6D6are the same as that of C6D6, find the resolution of C6H5Dand C6D6.

(f) If we just increased the column length to increase N, what value of N and what column length would be required for a resolution of 1.000?

(g) Without increasing the length of the column, and without changing the stationary phase, how might you improve the resolution?

(h) When the solvent was changed fromCH3CN/H2O(30:70 vol/vol) toCH3CN/CH3OH/H2O(10:5:85), the relative retention for C6H5D andC6D6increased to 1.0088 and the retention factor for C6H6 changed to 17.0. If the plate number were unchanged, what would be the resolution?

Question:The graph shows retention data from aC8silica column with an acetonitrile/water mobile phase.


(a) What mobile phase composition provides greatest retention(k)for the components? Least retention? Coelution (equalk)of two components?

(b) Predict the retention time of each peak at 40%and60%acetonitrite. Draw a chromatogram (a "stick diagram" representing each peak as a vertical line) of the separation at each mobile phase composition.

(c) Would60%acetonitrile yield adequate resolution?

(d) Assuming Gaussian peaks, does the separation at60%acetonitrile have the attributes of a good separation?

To which kinds of analytes do these liquid chromatography detectors respond?

(a) ultraviolet

(b) refractive index

(c) evaporative light scattering

(d) charged aerosol

(e) electrochemical

(f) fluorescence

(g) nitrogen chemiluminescence

(h) conductivity

Suppose that an HPLC column produces Gaussian peaks. The detector measures absorbance at 254 nm. A sample containing equal moles of compounds A and B was injected into the column. Compound A E254=2.26×104M-1cm-1has a height h=128mm and a half-width w1/2=10.1mm. Compound B E254=168×104M-1cm-1has w1/2=7.6mm. What is the height of peak B in millimeters?

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free