F335 - MD Flashcards

1
Q

Why is a salt more soluble in water than hexane?

A

Water is polar, there for stronger intermolecular bonds between the salt and water can be made (ion dipole?). These are stronger than the instantaneous dipole-induced dipole IM forces between a non-polar solvent and the salt.

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2
Q

Name of benzene with an NO2 group?

A

Nitrobenzene

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3
Q

Name of benzene with NH2 group?

A

Phenylamine

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4
Q

Reagents, conditions and classification of: benzene to nitro benzene (NO2)

A
  • Concentrate nitric (V) and sulphuric (V) acids.
  • Below 55*C
  • Substitution
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5
Q

Reagents, conditions and classification of: Adding aldehyde (or ketone) to a benzene ring

A
  • Methanoyl Chloride (Or Ethanoyl Chloride, or any longer chain than 1 carbon)
  • Reflux
  • AlCl3
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6
Q

Reagents, conditions and classification of: Replacing SO2 Cl on a benzene ring with SO2 NH2

A
  • Ammonia
  • room temperature
  • substitution
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7
Q

Reagents, conditions and classification of: NHCOCH3 on a benzene to NH2

A
  • NaOH (aq)
  • heat under reflux
  • hydrolysis
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8
Q

Meaning of the term Pharmacophore:

A

The active part of the medicine molecule.

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9
Q

How is the Pharmacophore identified between two substances?

A

The part of one molecule that exactly matches a part of the other molecules

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10
Q

Name the technique that is used to study the shapes of molecules and the way in which they fit together:

A

Computer modelling

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11
Q

Key steps in Retrosynthesis

A
  • Target molecule: disconnection point is identified.
  • Synthon: molecules with different charges that theoretically could make the target molecules but aren’t existing chemicals.
  • Synthetic Equivalent: a real molecule that resembles the synthon and shares vital properties (e.g. ability to obtain a charge around a required atom of the molecule).
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12
Q

How do competitive enzyme inhibitors reduce the rate of an enzyme catalysed reaction?

A
  • Prevent formation of Enzyme-substrate complexes
  • As have similar structure to substrate so will fit into active site of enzyme but will not react (due to different structure).
  • Less substrate can bind with enzymes so the rate of reaction is decreased.
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13
Q

Are competitive enzyme inhibitors temporary or permanent?

A

Temporary.

Leaves enzyme so level of inhibition relies on relative concentration of substrate and inhibitor (as they’re competing)

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14
Q

How do Non-competitive enzyme inhibitors reduce the rate of an enzyme catalyst reaction?

A
  • Prevent formation of enzyme- product complexes i.e. Prevent substrate from reacting to form product.
  • Bind to allosteric site, distorts 3D tertiary structure of enzyme so can no longer catalyse reaction.
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15
Q

Are Non-competitive enzyme inhibitors temporary or permanent?

A

Permanent (except for in metabolic functions)

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16
Q

Nitrobenzene to Phenylamine conditions and reagents.

A
  • Tin Cataylst

- concentrated HCl

17
Q

Conditions and reagents for: Pheylamine to benzene with N2+ Cl-

A
  • Nitric (III) acid (HNO2)

- dilute HCl

18
Q

Conditions and reagents for Benzene to cylcohexane

A
  • Hydrogen (gas)
  • Finely divided Nickel
  • 300*C, 30 atm
    [hydrogenation]
19
Q

What is molecular recognition?

A

A substrate (natural neurotransmitter) has the correct size and shape to fit into a receptor, and will then form bonds at several forms to produce a response.