Spectrophotometry Flashcards

0
Q

What 3 amino acids absorb light?

A

Tyrosine, Tryptophan and Phenylalanine

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1
Q

What wavelength is the colour red?

A

~700nm

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2
Q

What wavelength does tyrosine absorb light at?

A

280nm

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3
Q

What wavelength do haem groups absorb light at?

A

400-450nm

550-610nm

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4
Q

What wavelength is the colour blue?

A

~500nm

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5
Q

What colour is at the wavelength ~700nm?

A

Red

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6
Q

There were 3 absorption bands at: 430nm, 260nm and 280nm - what three things would these correspond to?

A

Haem group, Nucleic acids, Tyrosine/Tryptophan/Phenylalanine

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8
Q

What light source is used for spectrophotometry between 200-350nm?

A

deuterium arc source, a halogen source is used for wavelengths above 300nm

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9
Q

What is the variation in the beer lambert law accounting for stray light?

A

Log{(I0 + S)/(I + S)}

This means that as absorbance increases, so does the margin of error from stray light,

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10
Q

What colour is at ~400nm?

A

Violet

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11
Q

What wavelength do nucleic acids absorb light at?

A

260nm

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12
Q

In the Beer-Lambert law, what 2 things is absorbance equal to?

A

Log(I0/I) and e.c.l

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13
Q

As the absorbance increases will there be a greater or lesser error from stray light?

A

Greater error

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14
Q

When analysing a mixture of 2 components with the goal of finding each of their concentrations, how should you form the beer-lambert equations?

A

A = ecl1 + ecl2

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15
Q

What colour is at ~500nm?

A

Blue

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16
Q

What is a standard curve used for?

A

Used for finding concentration, the beer-lambert Law is not necessarily accurate experimentally due to impact of stray light, as absorbance drops below expected value. Standard curves are used

17
Q

What is the Isobestic point used for?

A

Finding out the total concentration of a mixture of species - cannot discover individual species concentrations from this

18
Q

When analysing a mixture of 2 components, aiming to find the concentrations of both, what 2 values of each species do you require?

A

Molar extinction coefficient (species must have different coefficients) at 2 different wavelengths

19
Q

At what wavelength is it necessary to Quartz cuvettes?

A

Wavelengths BELOW 300nm

For longer wavelengths, optical glass may be used

19
Q

At the Isobestic point, what is the same for the 2 species?

A

When varying wavelength, the Isobestic point is the point at which two species have the same molar extinction coefficient