In gas chromatography (GC), why do we use a FAME standard instead of an alkane standard and how can we still use this to calculate a retention index?
If you use FAME polyethylene glycol column, 30 meters or 100 meters with temperature ramping starting from 50 oC to 225 oC with 3 oC increase per minute. Phenolic groups can be detected but not on the FAME column, but RTX5 should do the job for that using GC-MS.
Nitrogen content will be best estimated using the Kjeldahl apparatus.
The main advantage of FAME standard over alkane standard is that FAME is more polar than the alkane.
In gas chromatography (GC), why do we use a FAME standard instead of an alkane standard...
Which one would elute first on GC (gas Chromatography, hexane or toluene? why?
Lab #2: Gas Chromatography Theory behind gas chromatography What do all types of chromatography share in common? Relationship between retention time and boiling point/vapor pressure How changing parameters affect the retention time Ramp rate Temperature Length of column Pressure Whether column is packed or unpacked
All Questions are in regards to Gas Chromatography 1. Explain what injection splitting is and why it is necessary to use in this and all of our experiments. 2. What are adjusted and corrected retention data? (See text book and other references if needed) 3. Do you expect peak shapes to be the same for all the standards on column A? Assume column A is non polar such as polymethylsiloxane. Explain 4. What is and what is the advantage of...
I am confused with gas chromatography. The question I am being asked is why did we use column B (silicone oil) for separating 1-butene, trans-2-butene, and cis-2-butene from each other in a GC. I have answered all the other questions but I'm completely stuck on this one; can anyone help please?
For the three gas chromatography graphs in the picture, how do I calculate the ratio of Cl:Br? I believe it has something to do with the area of the peaks (given in the tables below the graphs). Also, how do I determine which is a better nucleophile and why? Thank you! Use this table to correlate the peaks in the GC printouts to product identification. Then use the table entries for area or area% in the GC results to calculate...
Table 2: Alcohol and Ketone Standards GC Retention Times GC#: Retention time Alcohol Standard Mixture Phent ion= 2.05Smin low Peak 1 Compound Name: athanol Rapesnal utanal aclapeatanal 4.755min oilng 6.895min .230 min Peak 2 Compound Name: Peak 3 Compound Name: Peak 4 Compound Name: GC#:1 Ketone Standard Mixture Retention time 2.575un Peak 1 Compound Name: Acclono Butanon a Pentanone 2tHex anon Peak 2 Compound Name: min Peak 3 Compound Name: 615 min 1D. 307 min Peak 4 Compound Name: Part...
Explain the various factors responsible for separation of components of a mixture in chromatography. Explain about the classification of chromatography with few examples. Draw a block diagram of gas chromatograph and explain the function of each component Write a note on the micro syringe use to inject the liquid sample into gas chromatograph. Write a note on principle of working of Gas chromatograph. (How to prepare GC for analysis) Write a note on analysis of chromatogram (Types the method of...
Why do we use Hg vapor for fluorescent light instead of Neon? Why do fluorescent lights use phosphors?
chromatography mechanisms -In ion-exchange mechanism of chromatography, let assume we use cation exchangers, cation will attract to stationary phase and remain binded untill we change th PH to get that cation my question is what I do with PH, raised it decrease it to get the cation? and why? -the same for the covalently binding of protein and antigen in affinity chromatography mechanism, how can I get the protein from antigen? is it by using PH (increa decrease)? of course,...
Why do we use an ANOVA instead of doing multiple T-tests?