3Halogenoalkanes Flashcards

(25 cards)

1
Q

What does anhydrous mean?

A

In the absence of water

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2
Q

What’s initiation

A

Radical forming step

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3
Q

What’s a nucleophile

A

Electron pair donor

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4
Q

What’s propogation

A

Spreading of the radicals

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5
Q

What’s a radical

A

Free radicals are reactive species with an unpaired electron and are drawn using a dot

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6
Q

What’s termination

A

All radicals are removed

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7
Q

What’s the order of the bond enthalpies from the strongest to the weakest?

A

C-F
C-Cl
C-Br
C-I.
Polarity also decreases

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8
Q

What are primary halogenoalkanes?

A

Have one R group attached to the carbon linked to the halogen

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9
Q

What’s a secondary halogenoalkane?

A

Two R groups are attached to the carbon linked to the halogen.

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10
Q

What’s a tertiary halogenolkane?

A

Have three R groups attached to the carbon linked to the halogen

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11
Q

Describe the solubility of a halogenoalkane

A

The polarity of the bond is not enough to make halogenoalkanes soluble in water, the main imfs are van der waals and dipole dipole attractions.

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12
Q

Describe the boiling point of a halogenoalkane

A

Increases with chain length
Increases going down the halogen group

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13
Q

What’s their trend in reactivity?

A

Reactivity increases going down the halogen group even though C-I is the least polar bond, this is due to their atom size.

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14
Q

What is nucleophillic substitution

A

When halogenoalkanes react with aqueous hydroxide ions
The nucleophile attacks the delta positive carbon and the bond between c and the halogen breaks and the halogen takes the electron.
The halogen results as a nucleophile.

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15
Q

What’s elimination?

A

When halogenoalkanes react with ethanolic hydroxide ions
The nucleophile attacks the hydrogen on the carbon adjacent to the carbon linked to the halogen. The C-H bond breaks and moves to the C=C as a double bond. This breaks the C- halogen bond and the electrons go to the halogen
The halogen results as a nucleophile

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16
Q

What are the products of nucleophillic substitution

A

Alcohol and a halogen ion

17
Q

What’s the products of elimination?

A

An alkene, halogen ion and a water molecule.

18
Q

The bond between the carbon and the halogen are always polar- which one is which?

A

C is always delta positive
Halogen is always delta negative

19
Q

How must nucleophiles be drawn

A

Lone pair of electrons
Negative sign

20
Q

What’s the most important thing to remember when dealing with arrows from nucleophiles?

A

The arrow should come from the lone pair

21
Q

What are the conditions for nucleophillic substitution?

A

Low temp (warm or cool)
An ion to act as a nucleophile
Aqueous conditions

22
Q

What are the conditions needed for elimination

A

Higher temp
Alcoholic- ethanolic acid
The ion acts as a base

23
Q

What does ozone do?

A

Absorb uv radiation

24
Q

Show an example of ozone depletion

A

03 + Cl* —> *OCl + 02
OCl + 03 —> 202 + Cl

Overall= 203 —> 302

25
What are common nucleophiles?
CN:- :NH3 -:OH