Which of the dyes in screen methyl orange is more soluble in water?
Methyl orange is an azo dye that exists in two forms: an acidic red form and a basic yellow form. The basic yellow form is more soluble in water compared to the acidic red form because it is anionic and can form hydrogen bonds with water molecules.
What are the causes of tailing in chromatography?
Tailing in chromatography can be caused by factors such as non-specific interactions between the analyte and the stationary phase, column overload, sample matrix effects, or inaccuracies in the injection process. These factors can lead to peak distortion, decreased resolution, and decreased sensitivity in chromatographic separations.
Polar and non-volatile compounds, such as large biomolecules like proteins or carbohydrates, can be separated by high performance liquid chromatography but not gas chromatography due to differences in their chemical properties and interaction with the stationary phase. Gas chromatography is more suitable for separating volatile and non-polar compounds based on their volatility and interaction with the stationary phase.
What is seal wash in high pressure liquid chromatography?
A seal wash in high pressure liquid chromatography (HPLC) involves flushing solvent through the seals of the pump to prevent contamination and deterioration of the seals over time. This helps maintain the integrity of the pump and prevents leakage, ensuring accurate and consistent results during sample analysis.
What could you do to tea to get sugar to dissolve more slowly?
You can stir or whisk the tea more gently to slow down sugar dissolution. Additionally, using larger sugar crystals or reducing the sugar concentration can also help it dissolve more slowly in tea. Finally, cooling the tea down before adding sugar can slow down the dissolution process.
What is rm value in chromatography?
The rm value (also known as retention factor) in chromatography is a measure of how strongly a compound is retained by the stationary phase relative to the mobile phase. It is calculated as the distance traveled by the compound divided by the distance traveled by the solvent front. The rm value helps in characterizing and identifying compounds based on their behavior in the chromatographic system.
What is a chromatography absorber?
Adsorptive chromatography is an analytical technique used for the chemical separation of mixtures and substances. The technique depends on the principle of selective adsorption (not to be confused with absorption), a type of adhesion.
Why could chromatography be used in investigating the crime?
Chromatography could be used in investigating a crime because it can separate and analyze complex mixtures of substances, such as drugs, poisons, or chemicals found at a crime scene. By identifying and comparing different compounds in samples, chromatography can provide valuable evidence to link suspects, victims, or locations to a crime.
Which solvent gives antimicrobial property?
Solvents like ethanol, isopropanol, and hydrogen peroxide are commonly used in disinfectants and hand sanitizers due to their antimicrobial properties. They can effectively kill bacteria and viruses when used in the right concentrations.
What happens when there is a letter change in DNA?
A letter change in DNA, known as a point mutation, can result in a different amino acid being incorporated into a protein during translation. This can potentially alter the structure and function of the protein. Depending on the location and type of mutation, it can lead to genetic disorders, diseases, or even beneficial traits in an organism.
What is role of ninhydrin in thin layer chromatography?
Ninhydrin is used as a visualization reagent in thin layer chromatography to detect amino acids and other compounds that contain primary amines. When sprayed onto the developed TLC plate and heated, ninhydrin reacts with primary amines to form colored products, allowing for visualization and identification of the separated compounds.
Is hplc chromatography reliable?
Yes, HPLC chromatography is a highly reliable technique for separating and analyzing compounds based on their physical and chemical properties. It is widely used in various industries such as pharmaceuticals, food testing, environmental analysis, and more due to its high sensitivity, accuracy, and reproducibility.
Could the presence of different pigments be detected before separation by chromatography?
Yes, the presence of different pigments can be detected before separation by chromatography through techniques such as UV-Vis spectroscopy or fluorescence spectroscopy. These techniques can provide information about the absorption or emission properties of the pigments present in a sample.
The Screened Methyl Orange moves the furthest
How does perfusion chromatography work?
Perfusion chromatography is a technique
arised
to overcome the problem associated with mass transfer in the separation
of large
molecules such as proteins by high-performance
liquid chromatography (HPLC). Perfusion media are constituted by
two set of pores:
•throughpores
(6000--8000 A
°
)
•
diffusive pores
(800--1500 A
°
) which enable better access
of.
Macromolecules
to the inner of the particle by the combination of convective and diffusive flow.
General
characteristics of
perfusion
chromatography
In conventional liquid chromatography (diffusion chromatography) molecules move to the outer surface of the stationary phase particles by convection which constitutes a rapid step Nevertheless, transport of molecules through a stationary phase particle occurs by molecular diffusion which constitutes a very slow process, especial
ly
in the case of peptides and proteins that present high molecular weights and low diffusion coefficients . As a consequence, a significant increase in bandspreading (loss in resolution) could occur.
In perfusion chromatography (flow-through particle chromatography), stationary phase particles
used are designed to enable a better access of molecules to the inner of these through two classes of pores:
throughpores
(6000–8000 A
°
), which cross
damthe
stationary phase particle from side to side and allow the transport of molecules into the interior of the particle by convective flow and
diffusive pores
(800–1500 A
°
), interconnecting the
throughpore
network and enabling the transport by diffusion In this way, molecules travel by convection
through the column to the stationary phase particle, such as in conventional chromatography. Since there, molecules cross the stationary phase particles by means of a combination of convective and diffusive transport, thus, accelerating the transport of molecules through the particle. This singular bimodal structure significantly enhances mass transport of molecules...
Why do colours separate in chromatography?
Colors separate in chromatography because different compounds have different affinities for the stationary phase and the mobile phase. As the mobile phase travels through the stationary phase, compounds are carried at different rates based on their interactions with the two phases. This results in the separation of the compounds based on their unique properties.
What is true about chemical reactions in a closed system?
In a closed system, matter cannot enter or leave the system, but energy can still be exchanged with the surroundings. Chemical reactions in a closed system will reach equilibrium, where the rates of the forward and reverse reactions are equal and the concentrations of reactants and products remain constant. The total amount of matter in the system will not change during a reaction in a closed system.
Why you use silica gel in chromatography?
Silica gel is commonly used in chromatography as a stationary phase due to its high surface area and ability to adsorb a wide range of compounds. It provides good separation of components based on their size, polarity, and interactions with the silica surface.
How do we remove co2 from a mixture of gases?
Carbon dioxide can be removed from a mixture of gases through various methods such as absorption, adsorption, membrane separation, or cryogenic distillation. These processes selectively capture CO2 molecules from the gas mixture, allowing for separation and removal.
Can you separate 2 compounds with similar retention time in a gas chromatography?
Yes, compounds with similar retention times in gas chromatography can be separated by using different stationary phases or adjusting the temperature gradient of the column. Additionally, using a tandem technique like gas chromatography-mass spectrometry (GC-MS) can help in identifying and separating the compounds based on their mass spectra.
Which sugar are present and not present in the fruit juice?
Fruit juice naturally contains fructose and glucose sugars from the fruit itself. Sucrose, a disaccharide made up of fructose and glucose, may also be present depending on the fruit processed. Lactose, a sugar found in dairy products, would not typically be present in fruit juice unless it has been added during processing.
Why time recorded when half of sulphuric acid ran into reactant mixture?
The time is recorded when half of the sulfuric acid is added to the reactant mixture because it marks the halfway point of the reaction. This allows for better control of the reaction progress and timing of subsequent steps. It also helps to ensure that the reaction proceeds as planned and that the desired outcome is achieved.
Why NH group is more reactive than OH group?
The NH group is more reactive than the OH group because the lone pair on nitrogen in NH group is less stable due to the higher electronegativity of nitrogen compared to oxygen. This makes the lone pair in the NH group more readily available for reactions compared to the OH group. Additionally, the smaller size of nitrogen allows for stronger interactions with other atoms or molecules, increasing reactivity.