3.3.3 Halogenoalkanes Flashcards

1
Q

Reactivity of halogenoalkanes

A

Much more reactive than alkanes

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2
Q

Uses of halogenoalkanes

A

Refrigerants,
Solvents
Pharmaceuticals

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3
Q

Are halogenoalkanes polar or non-polar

A

Polar due to high electronegativity difference between halogen atom and carbon it is bonded to

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4
Q

Nucleophile definition & 3 examples

A

‘Positive loving’ - an electron rich species that can donate a pair of electrons to form a covalent bond
:NH3
:OH-
:CN-

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5
Q

What makes more of a difference in halogenoalkane reactivity - bond enthalpy of electronegativity difference

A

Bond enthalpy, the larger the atom, the weaker the bond, so the lower the bond enthalpy. Iodine has fastest rate of reaction.

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6
Q

Conditions that favour substitution

A

Water solvent
Lower temperature
Lower conc of NaOH/KOH

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7
Q

Conditions that favour elimination

A

Ethanol solvent
Higher temperature
Higher conc of NaOH/KOH
Reflux

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8
Q

Carbocation definition

A

Hydrocarbon molecule in which one of its carbon atoms is only bonded to three other atoms and has a positive charge.

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9
Q

Elimination reaction definition

A

A reaction in which an atom or a group of atoms in a compound is removed from a molecule.

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10
Q

How does NaOH act as a nucleophile and a base

A

Base - Completely ionises water.
Nucleophile - it can donate a pair of electrons

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11
Q

What carbocation is the most stable

A

Tertiary as there is more of an inductive group due to 3 alkyl groups

tertiary > secondary > primary > methyl

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12
Q

Why is ozone beneficial

A

It absorbs ultraviolet radiation

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13
Q

What do CFC’s do

A

Form chlorine radicals which catalyse the decomposition of ozone

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14
Q

Depletion of ozone equations

A

Cl2 –> 2Cl*
Cl* + O3 –> ClO* + O2
ClO* + O3 –> 2 O2 + Cl*

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15
Q
A
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