Electrophilic addition Flashcards

1
Q

Bond angle of the C-H in a single bond? (Alkane)

A

109.5 degrees

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2
Q

Bond angle of the C-H in a double bond?

A

120 degrees

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3
Q

Why are alkanes less reactive than alkenes?

A

Alkenes and alkynes are generally more reactive than alkanes due to the electron density available in their pi bonds. In particular, these molecules can participate in a variety of addition reactions and can be used in polymer formation

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4
Q

What are the four stages of free radical substitution?

A

1- initiation
2-propagation a
3-propagation b
4- termination

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5
Q

What happens during initiation?

A

Free radicals are produced.

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6
Q

What occurs at the stage of propagation?

A

Radicals react and form different free radicals

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7
Q

What happens in termination?

A

Combination of the free radicals, forming a stable product

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8
Q

What is hetrolytic bond fission?

A

A convalent bond is broken and the shared pair of electrons is taken by one of the atoms

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9
Q

What is homolytic bond fission?

A

The even breaking of a bond, where each atom takes away one electron to form radicals.

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10
Q

What is a primary stucture?

A

When the there is only one CH3 added to the compound

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11
Q

What is a secondary structure

A

Where there are 2 CH3 groups either side of the compound

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12
Q

What is tertiary structure?

A

Where there are 3 CH3 groups branched of the central carbon chain

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13
Q

Why is a pi bond weaker than a sigma bond?

A

a pi bond requires less energy to be broken, the overlap of the atomic orbitals in the pi bond is a sideways overlap which is a weaker overlap compared to the sigma bond which is a head-on overlap.

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