Module 4 - Alkenes Flashcards

1
Q

What are alkenes?

A

Unsaturated hydrocarbons that contain
at least one C=C bond made up of a 𝜋
bond and a 𝜎 bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the general formula of
alkenes?

A

CnH2n

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How is a 𝜋 bond formed?

A

Electrons in the adjacent p orbitals
overlap above and below the carbon
atoms. They can only be made after a 𝜎
bond is formed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What bond restricts the
rotation of carbon atoms?

A

𝜋 bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the angle and shape
of a double bond?

A

Trigonal planar
120°

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Are they more or less reactive
than alkanes? Why?

A

More reactive due to high electron
density of double bond and the fact the
pi-bond is slightly easier to break

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What intermolecular forces of
attraction do they have?

A

Only London forces due to non-polar
bonds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Are they soluble in water?
Why?

A

No, non-polar bonds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Write an equation for the
complete combustion of
pent-2-ene

A

CH3CH=CHCH2CH3 + 7½O2→ 5CO2+ 5H2O

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the types of isomers
that can be formed using
alkenes?

A

E/Z isomers - due to the restricted
rotation
Cis-trans isomers - if two of the same
substituents are attached to each carbon

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is an electrophile?

A

Species that are electron pair acceptors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the most stable type of
carbocation intermediate?
Why?

A

Alkyl groups have a positive inductive
effect, so the most stable carbocation is
the one bonded to the most other carbon
atoms i.e. A tertiary carbocation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Major products will be formed
from which kinds of
carbocations?

A

Tertiary (or the most stable available)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What conditions are needed
for the electrophilic addition of
H2O to an alkene? What is this
type of reaction called?

A

Steam in the presence of an acid catalyst,
usually phosphoric acid
Reaction is called hydration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the product(s) of the
hydration reaction?

A

An alcohol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What conditions are needed
for the electrophilic addition of
a hydrogen halide to an
alkene?

A

Hydrogen halide gases must be at room
temperature

17
Q

What is the reaction called
when a halogen is added to
alkene?

A

Halogenation

18
Q

How does a molecule with a non-polar bond react as if it is an
electrophile?

A

C=C double bond with a high electron
density induces a temporary dipole in the
halogen molecule → δ+ atom attracted
to double bond

19
Q

How can an alkene be
converted into alkane? What is
the reaction called and what
are the required conditions?

A

Alkene + hydrogen = Alkane
Hydrogenation
Conditions → 150°C, nickel catalyst

20
Q

What is an addition polymer?

A

Many monomers bonded together via
rearrangement of bonds without the loss
of any atom or molecule

21
Q

What are monomers? What
form do they usually take?

A

Molecules which combine to form a
polymer
Usually have a C=C bond which breaks
to leave a repeating pattern

22
Q

What are the ways in which
plastics can be disposed?

6 points

A

● Landfill
● Combustion
● Electricity generation
● Reuse
● Recycle
● Organic feedstock

23
Q

What are the disadvantages of
recycling?

A

● Plastics must be sorted into different types
● Expensive
● Labour intensive
● Requires high technology

24
Q

How does photodegradable
polymers break down?

A

They are broken down chemically using
energy with wavelengths similar to light.
Once the break down begins it is not
possible to stop the process

25
Q

Explain what happens in
organic feedstock

A

Plastics are separated and broken down into
small organic molecules through a series of
reaction. The molecules can then be used
produce plastics and in other industries