alkenes Flashcards

1
Q

what is a hydrocarbon?

A

Compound containing carbon and hydrogen only

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

What is saturated?

A

only has single bonds

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

what is unsaturated?

A

Contains carbon-to-carbon multiple bonds.

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

What is a homologous series?

A

a family of compounds with same general formula and functional group but each successive member differs by CH2

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

Functional group

A

Atom or groups of atoms responsible for molecules chemical properties.

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

How are pi bonds formed?

A

Formed by sideways overlap of two P orbitals, one from each carbon atom of double bond.

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

what is the shape around double bond?

A
  • Three regions of electron density around each carbon atom.
  • Three regions repel each other as far as possible so the bond angle around each carbon atom is 120 degrees.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what does E/Z isomerism involve?

A
  • A c=c bond.
  • Different groups attached to each carbon of the double bond.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is stereoisomers?

A
  • Have same structural formula but a different arrangement of atoms in space.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

reaction of alkenes with hydrogen.
- change in functional group
- conditions
- type of reaction

A

alkene -> alkane
condition -> nickel catalyst
type of reaction -> addition/reduction

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

reaction of alkenes with bromine/chlorine
-change in functional group
- conditions
- reagent
- type of bond fission

A

alkene -> dihalogenoalkane
conditions - room temp
reaction - electrophilic addition
bond fission - heterolyctic
reagent - electrophile

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

what is an electrophile?

A

an electron pair acceptor

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

reaction of hydrogen bromide/ hydrogen chloride with alkanes
- change in functional group
- mechanism
- conditions
- reagent
- type of bond fission

A

alkene -> halogenoalkane
condition -> room temp
mechanism -> electrophilic addition
reagent -> electrophile
type of bond fission -> heterolyctic

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

reaction of alkenes to form alcohols
reagent
conditions

A

reagent - steam
conditions - high temperature 300 to 600 degrees Celsius
high pressure 70 atm
catalyst of concentrated phosphoric acid

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

How to test for alkenes?

A
  • Test for unsaturation.
  • Bromine water will change from orange to colourless once shaking.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is markownikovs rule?

A

H always add on to the side that has the most hydrogen, as this forms the most stable carbocation intermediate.

17
Q

What the most stable alkene and least stable alkene?

A

most stable - primary alkene
least stable - tertiary alkene

18
Q

Reactivity of alkenes.

A

Much more reactive than alkanes because the presence of the pi-bond.
- Being on the outside of the double bond, the pi- electrons are more exposed than the electrons in the sigma-bond.
- A pi bond readily breaks and alkenes undergo addition reactions relatively easily.