Alkenes Flashcards

1
Q

What is the general formula for alkenes?

A

CnH2n (same as cycloalkanes)

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

What is the shape around carbon atoms in alkenes?

A

Trigonal planar

120 degrees

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

What are structural isomers?

A

Same molecular formula, different structural formula

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

What are stereoisomers?

A

Same molecular formula and structural formula but a different 3D arrangement

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

What are Pi bonds?

A

P orbitals on adjacent carbon atoms overlap sideways to form a Pi bond above and below the plane of bonded carbon atoms

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

Definition of localised electrons

A

Electrons that are spread over 2 atoms or less

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

Definition of delocalised electrons

A

Electrons that are spread over more than 2 atoms (Eg benzene)

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

How do you work out E/Z isomerism?

A

Circle the group on each side of the C=C with the highest atomic number
If they are the same side then (Z)
If opposite sides (E)

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

What 2 things do you need in order for something to display E/Z isomerism?

A

C=C double bond (restricted rotation)

Each carbon in C=C double bond must have 2 different groups

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

What other molecules can display E/Z isomerism even though they don’t have a C=C double bond

A

Cycloalkanes as they have restricted rotation

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

What do you need in order for there to be Cis/trans isomerism?

A

C=C double bond

Look for 1 group that is on both sides

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

When are things Cis isomers?

A

When the group that is on both sides of the C=C is the same side (both bottom/both top)

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

When are things Trans isomers?

A

When the group that is on both sides of the C=C are different sides (one bottom, one top)

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

What is more reactive sigma or pi bonds?

A

Pi bond as they are weaker so easier to break/need less energy
Also areas of high electron density so attract positive things.

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

What is the first step of electrophilic addition?

A

Add dipoles to molecule your’e adding
Draw arrow from
Double bond to delta positive atom
Bond in molecule to delta negative atom

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

What is the second step of electrophilic addition?

A

Add delta positive atom to organic
Leftover carbon is carbocation (add a +)
Draw negative ion with lone pair of e-
Draw arrow from lone pair to carbocation

17
Q

What is the third step of electrophilic addition?

A

Draw complete structure

18
Q

What is an electrophile?

A

Atom/group of atoms that can accept a pair of electrons forming a new covalent bond
They are attracted to areas of lots of electrons

19
Q

When is Markownikov’s rule used?

A

When 2 or more products can be made

It is all about the stability of the carbocation and how that determines the major product

20
Q

What is the most stable carbocation?

A

Tertiary

21
Q

What is the least stable carbocation?

A

Primary

22
Q

Which is the major product, the most stable or the least stable?

A

Most stable

23
Q

What are polymers?

A

Chains made of lots of monomers (alkenes)

24
Q

What are made from polymers?

A

Plastics and fuels

25
Q

What is the reaction called when making a polymer?

A

Polymerisation

26
Q

How do you name polymers?

A

Put poly(the name of the alkene used)

27
Q

What happens to viscosity as saturation increases?

A

It increases