Lecture 7 Flashcards

1
Q

In the free radical mechanism how are bonds broken?

A

By Homoylsis.

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2
Q

What is homolysis?

A

Breaking of bonds into 2 equal parts.

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3
Q

Homoylsis is common in what type of bonds?

A

Non polar bonds.

No charge on atoms.

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4
Q

What is needed for a free radical mechanism?

A

U/V light- ENERGY

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5
Q

What happens in the initiation step in a free radical mechanism?

A

Radicals are produced.

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6
Q

What happens in the propagation step in a free radical mechanism?

A

Radials react with substrate- New radicals are produced so the reactions continues.

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7
Q

What happens in the termination step in a free radical mechanism?

A

Two radicals combine.

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8
Q

What happens in bond formation between radicals?

A

Each atom DONATES one electron to form a two- electron bond.

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9
Q

In fatty acid and prostaglandin biosynthesis what is needed to start the reaction?
What is produced? How?

A

Enzyme.

Radical is produced as hydrogen is removed.

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10
Q

Damage to DNA can cause CANCER. Small amounts of H2O2 in metabolism produce what radicals? Why?

A

OH radicals because of the weak O2 bond.

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11
Q

What substance prevent radicals from completing a harmful reaction? How?

A

Antioxidants.

Radical reacts with the antioxidant to form a stable radical so they don’t react with a biological molecule.

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12
Q

What enzyme has been developed to make use of reactivity of radicals?

A

CP450

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13
Q

In polar/ ionic mechanisms how are bonds broken?

A

Heteroylsis

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14
Q

In polar/ ionic mechanisms which atom to the electrons move to?

A

The most electronegative atom.

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15
Q

What is heterolysis?

A

One species takes both electrons.

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16
Q

What is an electrophile?

A

Electron lover/ Vacant Orbitals

Fully positive/ slightly positive.

17
Q

What is a nucleophile?

A
Nucleus lover (Positive)
Lewis bases or lone pair of electrons.
18
Q

Are carbocations electrophiles/ nucleophiles? Why?

A

Electrophiles

Carbon centre is electron deficient.

19
Q

Are carbanions electrophiles/ nucleophiles? Why?

A

Nucleophiles

Contain an electron- rich carbon centre.

20
Q

How is the movement of electrons show?

Where does it start from?

A

Curly arrow

Starts with electrons to wherever they are going.

21
Q

What is an addition reaction?

What happens to pie bond in these reactions?

A

Reaction where a SMALL molecule is ADDED to the starting material.

Broken.

22
Q

What is an elimination reaction?

What happens to pie bond in these reactions?

A

Involves REMOVAL of atoms/ groups from 2 ADJACENT atoms in the substrate molecule.

Formed.

23
Q

What is an oxidation reaction?

A

REMOVAL of H2 or INTRODUCTION of OXYGEN

24
Q

What is an reduction reaction?

A

ADDITION of H2.

25
Q

What is a condensation reaction?

A

Reaction involves COMBINATION of two molecules with ELIMINATION of a second small molecule. Addition- Elimination Reaction.

26
Q

What is a substitution reaction?

A

An atom or group directly attached to a carbon in the substrate molecule is REPLACED by another atom or group.

27
Q

What is a rearrangement reaction?

A

Molecule undergoes REORGANISATION of bonds to yield an isomeric product.