Lab Questions Flashcards

1
Q

How is the Rf value calculated?

A

Rf = distance of spot/distance of solvent

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2
Q

Which compounds travel further on TLC plates?

A

Non-polar substances

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3
Q

If TLC liquid is more polar, do polar substances travel more or less distance?

A

More distance

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4
Q

What is the equation to find the concentration?

A

n = m/GFM

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5
Q

What are equivalents?

A

Equivalents assess which reactant is limiting and which is in excess

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6
Q

What details are needed for a correct graph?

A

Title
Labelled axises
Units on axis
Axis takes up half of graph paper

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7
Q

How does p-aminophenol become paracetamol?

A

P-aminophenol is acylated to form paracetamol

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8
Q

How is paracetamol purified?

A

By recrystallisation

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9
Q

Why is ethanoic acid water soluble?

A

Carboxylic acid is hydrophilic

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10
Q

Why is paracetamol not very water soluble?

A

Aromatic ring is hydrophobic

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11
Q

How is para-aminophenol formed?

A

Phenol is nitrated to form ortho and para nitrophenol
P and O nitrophenol are separated
P-nitophenol is reduced to p-aminophenol (NO2 becomees NH2)

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12
Q

How is percentage yield calculated?

A

% yield = recrystallised yield/actual yield x100

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13
Q

How can impurities be checked for?

A

Low MP and larger MP range

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14
Q

Why is sulphuric acid added to powered plant?

A

To convert the free base to a salt

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15
Q

Why was DCM used?

A

As an organic solvent to remove impurities as free base is in salt form so aqueous soluble

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16
Q

Why was anhydrous sodium sulphate used?

A

As a drying agent

17
Q

Why is the vitali-morin’s test done?

A

To test for the presence of tropane alkaloids

18
Q

What colour is the Vitali-morin’s test?

19
Q

Why was TLC done for the alkaloids?

A

To examine the the resulting alkaloids for the presence of atropine and hyoscine

20
Q

What can be concluded about hyoscine?

A

Hyoscine is very non-polar as it travelled very far up the plate

21
Q

Why was methanol added to the dried solid?

A

As an organic solvent to extract the free base

22
Q

Why are barbiturates acid?

A

They can donate a proton

23
Q

How is the barbiturate molecule stabilised?

A

Electrons are delocalised around the ring to stabilise the molecule

24
Q

Why was analysis done at different pHs?

A

To mimic different body parts

25
When are barbiturates ionised?
In basic solutions
26
How do barbital and phenobarbital differ?
Phenobarbital has an aromatic ring so is more lipophilic, has higher logP and is less water soluble than barbital
27
Why was the first solution scanned at multiple dilutions?
To construct an absorbance vs concentration calibration curve Used to determine concentration later in the experminent
28
Why was the spectrometer blanked?
To give λ max to analyse further dilutions
29
What happens to the concentration in aqueous as pH increases?
Drug aqueous concentration increases as pH increases
30
What happens to %ionisation as pH increases?
As pH increases, % ionisation increases as barbiturates are ionised in basic solutions
31
What does SMILES stand for?
simplified molecular-input line-entry system
32
Why molecular weight under 500?
Follows Lipinski's rule of 5
33
Why is logP not the best measure of lipophilicity of drugs?
logP can only be used for unionised molecules and most drugs are ionised at physiological pH
34
What is the percentage ionisation of a drug when pKa=physiological pH?
50%
35
What is the percentage ionisation of an acidic drug when pH = pKa + 2?
99%
36
What is the percentage ionisation of a basic drug when pH = pKa - 1?
90%
37
Why was concentrated ammonia added?
To convert the salt to a free base