Pharmacology Flashcards

1
Q

Define Co-ordinate bonding

A

a form of covalent bonding where one atom supplies both shared electrons to the bond.
e.g. Ocygen in H2O and Nitrogen in NH3

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2
Q

What structural cause results in desflurane being more slowly metabolised than isoflurane?

A

Desfluranes Fluourine is more electronegative than chlorine in isoflurane.
This makes the C-F bone more polarised than the C-Cl bond making it more ionic in character and stronger than the C-Cl bond.

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3
Q

When does polarization occur ?

A

When the cation (+ve) distorts the electron cloud of an anion (-ve). causes more electron charge between the two nuclei, thus producing a degree of covalent bonding.

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4
Q

Name the 3 types of intermolecular attraction

A
  1. Van Der waals forces: Weakest force. electrons in the outer shell may form an instantaneous dipole inducing an instantaneous dipole in a neighbouring atom.
  2. Dipole-Dipole attraction: Attraction between polar molecules.
  3. Hydrogen bonding
    Type of dipole-dipole. Strongest. Occurs when hydrogen is bound to a very electrongative atom e.g. oxygen or fluorine. Creates a strongly electronegative atom that then forms dipole-dipole attractions.
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5
Q

How can covalent bonds be broken ?

A
  1. Homolytic fission -> each element takes an electron to form a free radical.
  2. Heterolytic fission- One element takes all the electrons and two oppositely charge ions are formed.
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6
Q

Define a strong electrolyte

A

dissociate completely in an aqueous solution to form separate ions e.g. NaCl -> Na+ and Cl-. Very water soluble but poorly lipid soluble.

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7
Q

Define a weak electrolyte

A

Only some molecules dissociate completely in aqeous solution.
Ionisaztion may be pH dependant.

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8
Q

Which two functional groups are most important in allowing small organic molecules to act as weak electrolytes?

A

Carboxyl COOH and Amine NH2 groups

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9
Q

What is pKa

A

pKa is the pH at which the concentration of the proton donor form is equal to that of the proton acceptor form.

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10
Q

How do you derive pKa?

A

R-COOH ⇔ R-COO- + H+

as an example.

Proton donor (k1) ⇔ Proton acceptor (k2) + H+

At equilibrium K1 = K2

Rearrange

H+ = K1/K2

K1/K2 is the dissociation constant

Negative logarithim of K1/k2 = pKa

i.e. the pH at which the proton acceptor concentration is equal to the proton donator form.

K1/K2 = 1 at equilibrium

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11
Q

What is pH

A

The pH is equal to −log10 c, where c is the hydrogen ion concentration in moles per litre.

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12
Q

When are weak acids and bases ionised?

A

Weak acids are ionised above their pKa

Weak bases are ionised below their pKa

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13
Q

What is the pKa of thiopentol ?
Is it a weak acid or base?

A

pKa 7.6
Weak Acid

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14
Q

What is the pKa of propofol and is it acid or base?

A

pKa 11.0
Weak acid

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15
Q

What is the pKa of etomidate and is it acid or base?

A

pKa 4.2
Weak Base

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16
Q

What is the pKa of Ketamine and is it an acid or base?

A

pKa 7.5
Weak base

17
Q

What is the pKa of Paracetamol and is it acid or base?

A

pKa 9.4
Weak acid

18
Q

What is the pKa of Ibuprofen and is it acid or base?

A

pKa 4.9
Weak acid

19
Q

What is the pKa of Tramadol and is it acid or base?

A

pKa 9.4
Weak base

20
Q

What is the pKa of Fentanyl and is it acid or base?

A

pKa 8.4
Weak base