Lab 1:Separation and Identification of AA's via Paper chromatography Flashcards

1
Q

define the term mobile phase!

A

something that carries the solutes through the stationary phase.
L> usually a gas or liquid

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2
Q

Stationary phase?

A
  • solid or liquid coated support that is immobile
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3
Q

Whats the third component of chromatography?

A
  • solutes that are separated from the mixture.
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4
Q

Explain the characteristics of the chromatograph paper used in lab!

A
  • paper is made of cellulose which is a polymer made of sugar…has a lot of hydroxy groups which are polar and strongly bind water molecules through hydrogen bonding.
  • paper resembles a liquid coated solid.
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5
Q

interaction of mobile and stationary?

A
  • comprising of polar organic solvents will be passed through the stationary paper either ascending by capillary action or descending due to influence of gravity .
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6
Q

What happens when a solute is exposed to two immiscible liquids?

A
  • it will distribute into liquids according to its solubility in each.
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7
Q

The ratio of solubility in each liquid is called the distribution coefficient, K also called the partition coefficient. What is the formula?

A

k = solubility in mobile phase/ solubility in stationary phase

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8
Q

Polar solutes will interact stronger with ____ and less polar solutes will interact stronger with___.

A
  • stationary phase
  • mobile phase
    L> polar solutes will be retained in the paper earlier on and the less polar ones will travel further.
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9
Q

What is the formula for the retention or retardation factor?

A

Rf= distance solute migrates/ distance mobile phase travelled

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10
Q

What term best describes paper chromatography?

A

partition chromatography

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11
Q

Was ascending or descending chromatography used in this experiment?

A

ascending

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12
Q

Most aa’s will produce a ___ colour when reacting with ninhydrin. __ and ___ have the amino group as part of a ring and give a yellow colour.

A
  • purple
  • proline
  • hydroxyproline
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13
Q

What is the purpose of using two different solvent systems (pH’s) to develop the chromatogram?

A

to separate co-elating solutes in a system to identify if two solutes can be the same if the relationship sustains during development.
ie: show up same on one test
will they on a different one?

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14
Q

If 3 ul of 0.01M alanine (MW 89g/mol) is applied to a spot on paper how many micrograms of solute are present? How many milligrams? Show work!

A
3ul x 1mL/1000ul = 3x10^-3mL
3x10^-3mL x 1L/1000mL = 3x10^-6L 
M=moles/v 
moles= 0.01M x 3x10^-6L = 3x10^-8 moles 
3x10^-8 moles  x 89g/mol = 2.67x10^-6 g 
2.67x10^-6 g x 1x10^6 ug/1g= 2.67ug of alanine 
2.67ug x 1x10^-3mg/ug= 2.67x10^-3 mg
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15
Q

Why do aa’s structure change in response to pH’s of varying environments ?

A

they have both a basic amino group and an acidic carboxylic acid group…….they also have side chains that are basic, acidic, polar or non polar….protonation can lead to development of a net ionic charge which changes the polar nature of something

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16
Q

More ionic charge = the more nonpolar/polar therefore the material will bind /stronger/weaker to the polar stationary phase

A

polar

17
Q

Will an aa have a higher Rf value in a mobile phase that causes it to be more polar or non polar?

A

non polar because it will not be retained as easily by the polar stationary phase.